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Vacant positions posted in Danish/Ledige stillinger på dansk

Opslået Jobtitel Sted Kategori
25-Apr-2014 Supporter søges til Process support i klinikpakkeriet i Måløv
Clinical Supplies Packaging&Shipping (CSPS) i Måløv søger en ingeniør eller lignende, som vil blive ansvarlig for support af vores produktions- og lagerfaciliteter, samt optimering af processer i de forskel...

Supporter søges til Process support i klinikpakkeriet i Måløv

  • Produktion
  • Danmark - Måløv

Clinical Supplies Packaging&Shipping (CSPS) i Måløv søger en ingeniør eller lignende, som vil blive ansvarlig for support af vores produktions- og lagerfaciliteter, samt optimering af processer i de forskellige teams i klinikpakkeriet. Du vil blive en del af supportteamet og referer til teamlederen for support i CSPS.

Om afdelingen
Du bliver en del af klinikpakkeriet (CSPS) i Måløv sammen med 75 kollegaer, fordelt på 4 teams - en afdeling i konstant udvikling med mange spændende udfordringer. Vi har ansvaret for at pakke og distribuere produkter til kliniske studier over hele verden, og arbejder tæt sammen med resten af den kliniske Supply Chain i CMC for at nå vores ambitiøse mål om at levere produkter i høj kvalitet og til tiden til patienter i hele. Vi arbejder løbende på at optimere vores processer, nedbringe leadtime og brug af ressourcer ved hjælp af diverse LEAN værktøjer.

Jobbet
Som ansvarlig supporter for produktions- og lagerfaciliteter, skal du sikre, at disse til enhver tid er i compliance, samt lever op til de gældende forretningsbehov. CSPS har en produktionsfacilitet bestående af temperaturovervågede lokaler i både pakkeriet og forsendelsen, 6 mindre temperatur kontrollerede lagerrum (hhv. stuetemperatur og køl), samt et stort kølehøjlager. Det er en af dine vigtigste opgaver at sikre, at alle disse lokaler lever op til samtlige krav både kvalitets- og miljømæssigt, idet dette er afgørende for vores godkendelse til at producere. Du vil blive ansvarlig for både at foretage periodiske systemevalueringer og håndtere kvalitetsmæssige afvigelser (Non conformities).

Du vil yderligere være ansvarlig for at optimere brugen af faciliteten og iværksætte nødvendige tilretninger i forhold til konstant ændrede krav, sikre gennemførelse af valideringer og være ansvarlig indenfor dit område ved både interne og eksterne audits. Det forventes, at du driver diverse optimeringer og procesforbedringer indenfor dit område. For at opnå dette, arbejder du tæt sammen med ingeniører, håndværkere, kemikere, teknikere og andre i afdelingen, men har også en del andre samarbejdspartnere både på tværs af Novo Nordisk og eksternt.

Udover ansvaret for faciliteterne, vil du indgå i og drive projekter i vores supportteam. Projekterne vil tage udgangspunkt i nogle af afdelingens fokusområder, som bl.a. er konstant at forbedre processerne både i forhold til GXP, men også i forhold til øget effektivitet.

Vi tilbyder et udfordrende job med muligheden for stor indflydelse på den strategiske retning for, hvorledes vi bruger vores faciliteter i afdelingen, samt hvordan vi udvikler vores processer.

Kvalifikationer
Du er enten uddannet ingeniør eller har en lignende uddannelse og baggrund, hvor du har opbygget kompetancer indefor validering af farmaceutiske faciliteter og udstyr. Det vil være en fordel, hvis du yderligere har kendskab til automatik. Du har desuden god erfaring med GMP og ISO, har et udpræget kvalitetsmindset , og er detaljeorienteret. Du trives i et miljø, hvor der er mange nye udfordringer, og hvor der kan være mange bolde i luften på en gang.

Vi forventer , at du kan arbejde meget selvstændigt, men at du er en teamplayer med en positiv tilgang til udfordringerne. Du har et højt engagement, er fleksibel og ivrig for at skabe gode resultater.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Sofie Boeck på + 45 3075 1429.

Ansøgningsfrist
15. maj 2014

Danmark - Måløv Produktion
24-Apr-2014 Kemiker-vikar
Novo Nordisk skaber fortsat stor vækst og gode resultater. Derfor har vi brug for en processupporter med højt energiniveau og lederambitioner til vores Purification Plant i Kalundborg. Med udgangspunkt i din vi...

Kemiker-vikar

  • Produktion
  • Danmark - Kalundborg

Novo Nordisk skaber fortsat stor vækst og gode resultater. Derfor har vi brug for en processupporter med højt energiniveau og lederambitioner til vores Purification Plant i Kalundborg. Med udgangspunkt i din videregående uddannelse, din viden om kemi og din sans for kvalitet, får du en vigtig rolle i vores arbejde med at understøtte produktionen.

Din nye arbejdsplads er Novo Nordisks produktions-site i Kalundborg. Vi er 2.600 kolleger, der bl.a. producerer 50 % af verdens insulin. Du kan glæde dig til at blive del af en organisation, der altid stræber højere. Alle medarbejdere har naturligvis personlige udviklingsplaner, og vi har sat vores videndeling i system i formaliserede faglige netværk.

Her er tale om et 12 mdrs. barselsvikariat.

Om afdelingen
Dit nye arbejde handler om finrensning af det nye og spændende produkt Victoza i afdelingen PPIII. Du bliver en del af et team på 18 akademikere og teknikere. Vi har ansvaret for processer og udstyr. Det drejer sig bl.a. om kromatografiske søjler, fældning, centrifugering, organisk syntese og råvare/solvent blanderi.

Jobbet
I dette job vil du primært skulle arbejde med vores råvare solvent afsnit, som er et område under stor udvikling, og du vil derfor få mulighed for at forme og sætte retning for denne slags processer fremadrettet. Du supporterer operatørerne i driften og træffer hurtigt beslutninger, hvis der opstår uforudsete driftsstop eller afvigelser – og efterfølgende identificerer du årsagen, ved at bruge systematisk problemløsning og lean-værktøjer. Daglig rapportering og dokumentation er derfor også meget vigtige ingredienser i dit nye job. Herunder håndterer du store datamængder, som du forvandler til forståelige procesbeskrivelser, der viser sammenhænge mellem data og processer.

Kvalifikationer
Kemisk viden og forståelse af processer og udstyr. Du har en videregående kemisk orienteret uddannelse (fx kemi ingeniør), som gør, at du er god til kemi og forstår sammenhængen mellem processer og udstyr. Der er GMP i alt, hvad vi laver, så forståelse og kendskab til dette er et stort plus. Samtidig er du skarp på rapportering og dokumentation og i den sammenhæng er det vigtigt, at du kan lide at behandle og se på data. Derudover er det vigtigt, at du trives i en hverdag med højt tempo, hvor du har rigtig mange kontakter på alle niveauer og på tværs af faggrupper. Da tæt samarbejde er en grundlæggende forudsætning for vores succes, skal du også være udpræget team-player.

Gør dig synlig til et fremtidigt job i produktionen: Vi har løbende nye stillinger inden for processupport. Så er der ikke en stilling, der rammer plet lige nu, så giv din interesse til kende ved at lave en uopfordret ansøgning via novonordisk.com/UA.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Kim Ejlersen på + 45 3075 1099.

Ansøgningsfrist
8. maj 2014.

Danmark - Kalundborg Produktion
24-Apr-2014 Operatører til produktionen i Storkøbenhavn
Føler du dig hjemme i et miljø, hvor ambitionerne er høje og kvaliteten er altafgørende? Brænder du for hele tiden at forbedre din måde at arbejde på? Er du fuld af initiativ og handlekraft, og bliver du motive...

Operatører til produktionen i Storkøbenhavn

  • Produktions operatør
  • Storkøbenhavn

Føler du dig hjemme i et miljø, hvor ambitionerne er høje og kvaliteten er altafgørende? Brænder du for hele tiden at forbedre din måde at arbejde på? Er du fuld af initiativ og handlekraft, og bliver du motiveret af teamwork med gode kolleger?

Så er et job som operatør i Novo Nordisk, Product Supply, måske noget for dig. Her får du mulighed for at gøre en forskel for patienter med diabetes, hæmofili eller andre sygdomme. Samtidig giver vi dig chancen for at udnytte dit potentiale, da vi har fokus på personlig og faglig udvikling. Du kan se frem til et job med stort ansvar, hvor du skaber resultater i samarbejde med dine kolleger.

Product Supply er ansvarlig for produktionen af alle produkter, der sælges af Novo Nordisk. Det er vores opgave at sørge for, at produkterne er tilgængelige, når kunderne skal bruge dem. Vi sikrer også, at alle produkter lever op til de aktuelle kvalitetsstandarder. Product Supply beskæftiger ca. 9.500 medarbejdere. For at opretholde en position, som en af de bedste leverandører af farmaceutiske produkter, fokuserer vi kontinuerligt på at udvikle og forbedre vores måde at arbejde på. Derfor er vi også altid på udkig efter nye dygtige medarbejdere.

Vi søger nu operatører til vores produktion i Bagsværd, Gentofte, Måløv og Hillerød. Der er tale om både permanente og midlertidige stillinger af op til 24 måneders varighed. I din ansøgning bedes du venligst angive tydeligt, hvor du har mulighed for at arbejde, og hvorvidt du er interesseret i vikariater og/eller faste stillinger.

Alsidige operatørjob i alle dele af produktionen
Dine arbejdsopgaver som operatør er varierede, men hovedvægten i jobbet ligger på at betjene produktionsudstyret, sikre at produktionen kører gnidningsfrit og sørge for at produkterne lever op til kvalitets og myndighedskrav. For at efterleve disse krav vil du få til opgave at dokumentere og kontrollere dit arbejde. Ofte vil rengøring af produktionsfaciliteterne og udstyret også være dit ansvar.

Du kan glæde dig til en hverdag i et velfungerende team med 8-30 kompetente kolleger. Mange opgaver løser du i teamwork, hvor kollegialt sammenhold og godt humør er i centrum. Men du får også selvstændigt ansvar for at løse egne opgaver. Vi lægger vægt på udvikling af vores medarbejdere og giver dem løbende de faglige kvalifikationer, som kræves i vores specifikke produktion. Sådan får du mulighed for at deltage i relevante kurser, som også udvider dine fremtidige jobmuligheder i Novo Nordisk.

Du skal regne med, at du kommer til at arbejde på holdskift med skiftevis dag, aften og nattevagter samt weekendvagter, da det meste af vores produktion kører i døgndrift året rundt.

Kvalitetsbevidste og handlingsorienterede operatører
Du har måske erfaring med at arbejde i en produktion men din faglige baggrund er ikke så væsentlig. Det vigtigste er, at du tager ansvar og er meget bevidst om kvaliteten i dit arbejde. Du skal også være klar til løbende at tilegne dig nye færdigheder og til at håndtere de udfordringer og forandringer, som ligger foran dig. I vores produktion er samarbejde vigtigt, så du skal have en positiv indstilling og lysten til at løse opgaver i fællesskab med kolleger. Endeligt har du fair for teknik og IT.

Du har dansk, matematik og engelsk på mindst 9. klasses niveau og/eller en uddannelse som for eksempel industrioperatør, procesoperatør, håndværker eller lignende. For at komme i betragtning til et job hos Novo Nordisk, skal du sammen med dit CV og ansøgning, uploade dokumentation for både folkeskoleuddannelse og evt. anden videre uddannelse.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt ORC (Operatør Rekrutterings Centret) på +45 3079 7628. Telefontiden er onsdag klokken 9.00 - 11.00 samt fredag klokken 13.00 - 15.00.

Ansøgningsfrist
13. maj 2014.

Storkøbenhavn Produktions operatør
24-Apr-2014 Kemiker
Får du energi af udvikling og elsker du at stå i spidsen, når der skal ske forandringer? Og er du ambitiøs med det du gør og en udpræget ’can do’ type? I så fald er du måske vores nye kollega i PP Utility Suppo...

Kemiker

  • Produktion
  • Danmark - Kalundborg

Får du energi af udvikling og elsker du at stå i spidsen, når der skal ske forandringer? Og er du ambitiøs med det du gør og en udpræget ’can do’ type? I så fald er du måske vores nye kollega i PP Utility Support.

Om afdelingen
PP er en del af Novo Nordisks insulinproduktion (DAPI), hvor vi i PP leverer finrenset insulin (Detemir, Degludec og Liraglutide) til færdigvarefabrikker i hele verden. PP Utility Support dækker de 4 PP fabrikker og er en del af PP’s vedligeholdelsesafdeling. Vi er 12 i teamet, som består af operatører, teknikere og kemikere, og er kendetegnet ved at være selvkørende og fagligt stærkt. Vores mål er at sikre, at anlæggene for renset vand sprit kører stabilt.

Jobbet
Dit ansvar er at sikre drift af anlæg for renset-vand og spritanlæg i PP fabrikkerne. Det vil sige, at du følger op på driften og håndterer afvigelser, problemløsning og optimeringsprojekter i samarbejde med PP’s support-teams. Dine ansvarsområder er en kombination af at være på gulvet og at håndtere administrative opgaver ved skrivebordet. Opgaverne på gulvet er sammen med kolleger i og uden for teamet, hvor du ofte er den, der driver processen. Du er med til at sikre at dokumentationen er på plads og udarbejder forskellige produktionsrelaterede rapporter. Du bliver målt på din evne til at håndtere afvigelser og optimeringssager samt anlæggenes oppetid. Du sikrer din succes ved at være en holdspiller og udvise tro på tingene. I teamet formår du at få de andre med dig og i høj grad bidrage til en positiv tilgang til udvikling og optimering af processer. Din erfaring og dit kompetenceniveau afgør omfanget af opgaver og ansvar, hvilket gør det til et udfordrende job hvad enten du er nyuddannet eller har erfaring. Da det er en stilling med mange interessenter på tværs i organisationen, får du rig mulighed for at løfte din faglighed. Du vil arbejde efter LEAN og GMP principper i alle aspekter af processer og arbejdsgange.

Kvalifikationer
Du har en akademisk naturvidenskabelig uddannelse, for eksempel som kemiingeniør, maskiningeniør eller pharmaceut. Du har kendskab til GMP/ISO og LEAN. Du skriver og taler både engelsk og dansk. Gennem studiejobs eller lignende har du vist, at du er kendetegnet ved at være en team-player, der kan få andre med dig. Du motiveres af at være i et dynamisk og udviklende miljø, hvor der hele tiden er fokus på forbedring af både kompetencer og processer. Du går forrest og kender værdien af god dataanalyse og en systematisk tilgang. Du evner med dit gode overblik at håndtere en løbende prioritering af dine opgaver.

På Novo Nordisk’s site i Kalundborg, Vestsjælland, finder du et verdensklasse produktionsmiljø. Vi er stolte over at kunne sige, at vi producerer en væsentlig del af verdens insulin og er langt fremme, når det kommer til teknologi, systemer, metoder og processer. Site Kalundborg er arbejdsplads for mere end 2.400 dedikerede Novo Nordisk medarbejdere, hvilket gør det til det største produktions-site i Novo Nordisks globale produktionsnetværk. Novo Nordisk i Kalundborg er en by i byen og har et areal, der svarer til 270 fodboldbaner, hvilket er en imponerende størrelse. Området, som ligger omkring en times kørsel fra København, har enda eget vejnet og et fritidscenter, hvor medarbejdere kan motionere. Er du vores nye kollega, tør vi godt garantere dig nogle muligheder, du vil have meget svært ved at finde andre steder.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Casper Falkenberg på +45 3079 0374

Ansøgningsfrist
19. maj 2014

Danmark - Kalundborg Produktion
24-Apr-2014 Kemiker med viden om GMP
Brænder du for at arbejde med aseptisk produktion og GMP indenfor miljø hos verdens førende producent af insulin? Hvis du gør så har vi jobbet til dig. Grib muligheden for en karriere der kan bringe dig vidt om...

Kemiker med viden om GMP

  • Produktion
  • Danmark - Bagsværd

Brænder du for at arbejde med aseptisk produktion og GMP indenfor miljø hos verdens førende producent af insulin? Hvis du gør så har vi jobbet til dig. Grib muligheden for en karriere der kan bringe dig vidt omkring både fagligt, personligt og internationalt.

Om afdelingen
Du bliver en del af vores Miljø Support afdeling som består af 75 kolleger, som tæller både miljøsupportere og miljøassistenter. Vi ansvaret for den daglige miljøsupport, prøveudtagning og rengøring af hele vores produktion i Bagsværd, dvs. alle kvalificerede områder. Det er vores ansvar at miljøet til hver en tid lever op til gældende lovkrav og regler så vi kan producere 24/7.

Jobbet
Din fornemmeste opgave bliver at yde support til vores aseptiske produktion ud fra et miljømæssigt perspektiv. I tæt samarbejde med operatører, supportere, teknisk support samt QA løser du en bred vifte af opgaver lige fra procesforbedringer til afvigelsessager. Du sikre dermed at vores produktion kan producere 24/7.

Du spiller en nøglerolle i arbejdet med at sikre drift og frigivelse af produkterne. Det gør du ved være vores garant for at vores miljø altid lever op til gældende lovkrav og at vi altid er i compliance. Du vil også være med til at sætte retning når det kommer til GMP og hvor det er vi skal være særligt opmærksomme på hvor udviklingen går hen.

Kvalifikationer
Du har en relevant uddannelse såsom kemiker, farmaceut, ingeniør eller tilsvarende. Du skal have viden om GMP – gerne relateret til aseptisk produktion. Har du tilmed erfaring fra farmaceutisk produktion samt kendskab til LEAN, er det en fordel.

Som person er du en problemknuser, og du trives i en forandrelig hverdag, hvor din evne til at træffe beslutninger er helt essentiel. Det kommer også til udtryk i forbindelse med overholdelse af compliance som er fundamentet for vores eksistens og der er det vigtigt at du formår at balancere kvalitet og præcision.

Du skal være stærk på analyse, håndtering af data og på IT værktøjer. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Kamilla Vig Jensen på + 45 3075 6450 eller Steen Hasselbalch på + 45 3079 0383.

Ansøgningsfrist
18. maj 2014.

Danmark - Bagsværd Produktion
24-Apr-2014 Kemiker
Har du lyst til at sætte dit præg på en afdeling i rivende udvikling, hvor din primære rolle bliver at have fokus på kvalitet og compliance i et QC laboratorium? Så læs endelig videre, for vi søger en kvalitets...

Kemiker

  • Produktion
  • Danmark - Måløv

Har du lyst til at sætte dit præg på en afdeling i rivende udvikling, hvor din primære rolle bliver at have fokus på kvalitet og compliance i et QC laboratorium? Så læs endelig videre, for vi søger en kvalitets koordinator, som vil være en del af et ledelsesteam, hvor dit ansvar bliver at sikre, at vi altid er på forkant med kvaliteten og sikre, at vi er inspektionsparate. Du vil få mulighed for at forme jobindholdet og kan se frem til et job, hvor frihed, ansvar og din faglige udvikling går hånd i hånd.

Om afdelingen
Sammen med godt 50 yderst motiverede og dygtige kolleger skal du være med til at sikre, at afdelingen altid har det rette kvalitetsniveau. Afdelingen er et driftslaboratorium for tablet produktionen af hormoner og orale antidiabetes produkter. Afdelingen er en del af Biopharm QC området, som består af 6 QC afdelinger. Din nye afdeling er især kendetegnet ved en uformel tone og et godt sammenhold, hvor vi gerne hjælper hinanden med at nå fælles mål. Vi belønner engagement og giver den enkelte medarbejder plads til at udfolde og udvikle sig både fagligt og personligt.

Jobbet
Du bliver en del af afdelingens leder/stab-team, hvor dit fokus, i samarbejde med afdelingens ledelse, bliver at sikre det rette kvalitetsniveau, og hele tiden arbejde på at løfte kvalitetsniveauet for afdelingens dygtige og engagerede medarbejdere. Du skal sikre, at afdelingen til enhver tid er inspektionsparat til audits fra både interne og eksterne myndigheder. Du vil skulle indgå i et tæt samarbejde med QC-områdets øvrige kvalitetskoordinatorer i forhold til sparring samt fastsættelse af mål og retning for hele området. Alt i alt vil du kunne se frem til en spændende og udviklende stilling med gode muligheder for selv at påvirke din dagligdag og på sigt din fremtidige karriere.

Kvalifikationer
Du har helt sikkert solid erfaring med kvalitet og/eller GMP produktion eller QC-laboratorium, og du er nu klar til at tage et endnu større ansvar. Du har en relevant naturvidenskabelig uddannelse (Farmaceut, kemiingeniør, cand. scient. el. lign.). Dine gode kommunikationsevner og din udadvendte og afslappede personlighed gør, at det falder dig naturligt at skabe tætte relationer til mange mennesker og faggrupper. Det er vigtigt, at du har gode kommunikationsevner, fordi du som kvalitetskoordinator kommer til at bidrage væsentligt til det gode samarbejde med mange faggrupper. Det er endvidere vigtigt, at du arbejder systematisk og kan prioritere dine opgaver. Du har det store overblik, når du skal træffe kvalitetsmæssige beslutninger, men har også fagligheden med, så du kan dykke ned i detaljen om nødvendigt. For at få succes i stillingen skal du være engageret og udvise høj grad af selvstændighed. Du trives i en hverdag med høj intensitet og ser det som din fornemmeste opgave at få fulgt opgaverne til dørs.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling, som du vil have svært ved at finde andre steder.

Kontakt
Vil du vide mere om stillingen så kontakt Helle Bang på + 45 3079 0612

Ansøgningsfrist
15. maj 2014

Danmark - Måløv Produktion
24-Apr-2014 Studentermedhjælper
Studentermedhjælper til Steno Center for Sundhedsfremme Vil du være med til at udvikle nye tilgange til at mindske ulighed i sundhed og forebygge diabetes? - og har du lyst til at være en del af et konkret for...

Studentermedhjælper

  • Studerende
  • Danmark - Gentofte

Studentermedhjælper til Steno Center for Sundhedsfremme

Vil du være med til at udvikle nye tilgange til at mindske ulighed i sundhed og forebygge diabetes? - og har du lyst til at være en del af et konkret forsknings- og udviklingsprojekt om sundhedsfremme i udsatte byområder? Så skal du måske være vores studentermedhjælper?!

Steno Center for Sundhedsfremme er et forskningscenter, som udvikler ny viden, metoder og tilgange til sundhedsprofessionelle og andre aktører, som kan skabe bæredygtig social forandring til fremme for folkesundheden. Centeret integrerer social- og humanvidenskabelig forskning for at skabe nye tilgange på et område, som trænger til at blive videnskabeligt fornyet. Centerets ambition er at udvikle et nationalt og internationalt kraftcenter med fokus på social forandring.

Social Network Study – borgerinddragelse og sundhedsfremme

Steno Center for Sundhedsfremme fokuserer på forebyggelse af type 2 diabetes. I projektet lægger vi vægt på en teoretisk og metodisk tilgang til borgerinddragelse og sundhedsfremme i relation til socialt udsatte befolkningsgrupper og lokalsamfund. Brugen af social netværksanalyse gør det således muligt at identificere centralt placerede netværk og personer, som kan inddrages i lokalt definerede, kulturelt sensitive og dermed bæredygtige sundhedsfremmetiltag.

Stillingen

På Steno Center for Sundhedsfremme, Steno Diabetes Center, søger vi en studentermedhjælper til the Social Network Study. Arbejdet vil omfatte forskellige opgaver som litteratursøgning, transskription og anden databehandling. Der vil dog i den første tid være absolut hovedvægt på etnografisk feltarbejde og gennemførelse af semi-strukturerede interviews i forbindelse med et konkret projekt i Københavns Kommune. Ansættelsen er i gennemsnit tre dage om ugen, og løber frem til årets udgang. Der må påregnes en øget arbejdsindsats i de første måneder. Dele af arbejdet vil foregå på vores samarbejdsinstitutioner.

Din profil

• Du har en bachelor i et relevant fag, fx sundhedsfremme, sociologi, etnologi eller antropologi.

• Du har solid erfaring med brug af kvalitative metoder herunder feltarbejde med interviews.

• Du mestrer til fulde dansk og engelsk i skrift og tale.

• Du er kreativ, engageret, resultatorienteret og en god kollega.

• Du har faglig og menneskelig modenhed og kan både arbejde selvstændigt og i et tæt samarbejde i en tværfaglig gruppe, hvor en positiv indstilling og humoristisk sans er afgørende.

• Du er tolerant og kan kommunikere med folk med forskellig baggrund.

Det er desuden en fordel, hvis du har erfaring med at:

• arbejde på forskningsprojekter.

• arbejde i tværfaglige miljøer.

• har kendskab til arabisk, tyrkisk eller somali.

• arbejde med samfundsvidenskabelige metoder og teorier.

Ansøgning

Din ansøgning, på dansk eller engelsk, skal indeholde:

• Din motivation og baggrund for at søge stillingen (max 1 side)

• CV (max 2 sider)

Ansøgningen sendes elektronisk senest fredag 9. maj 2014, kl. 12.00. Stillingen ønskes besat snarest muligt.

Kontakt

Yderligere information fås fra Anette Hindhede tlf. 3079 7935.

Om Steno

Steno Diabetes Center er en af verdens førende institutioner inden for diabetesbehandling og forebyggelse. Steno ejes af Novo Nordisk A/S og er en 'not for profit' virksomhed, der arbejder i partnerskab med det danske sundhedssystem. Steno står for behandlingen af ca. 5.600 mennesker med diabetes. For yderligere oplysninger, se www.steno.dk.

Danmark - Gentofte Studerende
24-Apr-2014 Laborant
Har du lyst til at arbejde med karakterisering og HPLC i en spændende afdeling, som forestår og behersker en bred vifte af analytiske teknikker, så er dette job utvivlsomt noget for dig. Om afdelingen...

Laborant

  • Forskning og Udvikling
  • Danmark - Måløv

Har du lyst til at arbejde med karakterisering og HPLC i en spændende afdeling, som forestår og behersker en bred vifte af analytiske teknikker, så er dette job utvivlsomt noget for dig.

Om afdelingen
CMC Analytical Support er en afdeling med 67 medarbejdere dedikeret til analyse af Novo Nordisks portefølje af både diabetes og biofarmaceutiske proteiner i klinisk udvikling. Afdelingen udfører analyse og karakterisering af peptider, proteiner, råvarer og lækstoffer. Afdelingen er en del af CMC Drug Product Development i R&D og bor i moderne laboratorier i Måløv.

Jobbet
Du vil primært arbejde med strukturopklaring af produkter og urenheder ved LC-MS (og evt. NMR) samt peptid mapping ved HPLC/UHPLC. I stillingen kommer du til arbejde med udvikling og validering af analysemetoder samt frigivelsesanalyser. Det meste af din tid vil du bruge i laboratoriet, men du vil også være ansvarlig for databehandling og afrapportering af de opnåede resultater. Du vil arbejde tæt sammen med både kemikere og andre laboranter på tværs af Novo Nordisks projekt portefølje. Herudover vil du deltage i øvrige laboratorieopgaver, som f.eks. vedligeholdelse inkl. kvalificering af udstyr samt udarbejdelse af instruktioner.

Da vi arbejder under GMP, er en omhyggelig dokumentation en selvfølge.

Vi optimerer løbende vores arbejdsprocesser via LEAN og du forventes at være engageret i arbejdet med problemløsning og optimeringer sammen med dine kollegaer. Sproget i det daglige er dansk, men vi forventer at du kan både skrive og læse engelsk på teknisk/fagligt niveau.

Kvalifikationer
Du har en uddannelse som laborant eller lignende. Du har mindst 2-3 års solid erfaring inden for strukturopklaring af peptider/proteiner ved LC-MS (f.eks. Orbitrap og Synapt) og MALDI. Du har erfaring med HPLC/UHPLC og gerne peptid mapping. Du er kvalitetsbevidst og har gerne GMP erfaring. Du kan arbejde selvstændigt og kan lide at tage ansvar for analyser og udstyr. Du skal kunne veksle mellem at arbejde på flere forskellige projekter med fokus på selve analysen fra prøveforberedelse til afrapportering af resultatet. Du skal udvise fleksibilitet i en hverdag, hvor opgaverne hurtigt kan blive omprioriteret i overensstemmelse med teamet. Du har en god struktureret tilgang til arbejdet og har lyst til at arbejde sammen med flere forskellige kemikere. Det er yderligere en fordel, at have erfaring med andre teknikker som NMR, sekventering, og gelelektroforese samt erfaring fra pharmaceutisk industri.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel.

Kontakt
Vil du vide mere om stillingen, så kontakt Marianne Olsen på + 45 3079 2650 eller Camilla Schmidt på + 45 3079 5479

Ansøgningsfrist
7 maj 2014.

Danmark - Måløv Forskning og Udvikling
24-Apr-2014 Administrativ QA assistent
Vi søger en ambitiøs administrativ assistent med reference til afdelingslederen i Biopharm QA QC & Support. Om afdelingen...

Administrativ QA assistent

  • Kvalitetssikring
  • Danmark - Gentofte

Vi søger en ambitiøs administrativ assistent med reference til afdelingslederen i Biopharm QA QC & Support.

Om afdelingen
Du skal have lyst til at arbejde for en mellemstor Quality Assurance afdeling, hvor trivsel og høje ambitioner går hånd i hånd. Vi er placeret i Gentofte, men har aktiviteter på andre sites.

Afdelingen beskæftiger sig med kvalitetssikring af Quality Controle analyse aktiviteter og Manufacturing Development opgaver.

Jobbet
Du er ledelsens højre hånd og yder højt kvalificeret support og sikrer en velfungerende infrastruktur.

Du skal kunne lide at arbejde selvstændigt og synes om at løse praktiske opgaver, der letter hverdagen for andre. Du ser ofte selv, hvor du kan gøre en forskel, og tager initiativet til dette.

Stillingen består hovedsagligt i at udføre de administrative opgaver, der støtter afdelingen til at nå dens mål. Dette omfatter dels en række faste administrative opgaver for afdelingen, såsom vedligehold af afdelingsmappe, og løbende opdatering af vores GlobeShare sider. Endvidere vil der være praktiske opgaver for afdelingslederen, såsom opfølgning på udvalgte afdelingsmål, faste evaluerings opgaver og budgetopfølgning. Desuden vil du være en nøgleperson i planlægningen og afviklingen af den praktiske side af myndighedsinspektioner i Biopharm.

Endelig er jobbet kendetegnet ved en række ad hoc opgaver så som afregning i Concure og ICE, samt administration af nyansættelser og fratrædelser.

Udfordringen er at sikre, at alle afdelingernes administrative processer altid er ”up to date” samtidig med at kollegerne i afdelingen oplever en god og målrettet hjælp til de administrative opgaver, der tilgår løbende.

Du ser en udfordring og en mission i at forbedre samarbejdsrelationer i og uden for afdelingen. Samarbejdet i funktionen, og med resten af Biopharm, er vigtigt. Du skal derfor have lyst og evne til at kommunikere, være fleksibel og initiativrig. Du vil være en aktiv deltager i Biopharm QA´s administrative medarbejders netværk.

Arbejdet foregår i et afslappet og uformelt miljø, hvor vi lægger vægt på trivsel, vilje til at gøre en forskel, humor og engagement.

Kvalifikationer
Du har en relevant administrativ uddannelse og gerne flere års erfaring. Du har erfaring med IT systemer inklusiv MS Office. Du har allerede demonstreret overbevisende resultater og en ambitiøs tilgang til dit arbejde.

Dine opgaver kræver både selvstændighed og evne til at kommunikere, og du skal have gode formuleringsevner i både skrift og tale.

Som person er du engageret og struktureret med et positivt livssyn og trives med mange store udfordringer.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Ulla Thinggaard på + 45 3075 2104.

Ansøgningsfrist
14. maj 2014

Danmark - Gentofte Kvalitetssikring
23-Apr-2014 Pakkeriassistent
Har du lyst til at være en del af et team, som har ansvaret for pakning af kliniske produkter, som pakkes i henhold til GMP? Kan du holde overblikket og bevare roen i en hverdag, som kan være både hektisk og om...

Pakkeriassistent

  • Produktions operatør
  • Danmark - Måløv

Har du lyst til at være en del af et team, som har ansvaret for pakning af kliniske produkter, som pakkes i henhold til GMP? Kan du holde overblikket og bevare roen i en hverdag, som kan være både hektisk og omskiftelig?

Så er du måske en af den nye engagerede kollega, vi søger i Clinical Supplies Packaging(CSP) i Packaging teamet, som er en del af CMC.

Om afdelingen
Du bliver en del af klinikpakkeriet (CSPS) i Måløv sammen med 75 kollegaer, fordelt på 4 teams - en afdeling i konstant udvikling med mange spændende udfordringer. Vi har ansvaret for at pakke og distribuere produkter til kliniske studier over hele verden, og arbejder tæt sammen med resten af den kliniske Supply Chain i CMC for at nå vores ambitiøse mål om at levere produkter i høj kvalitet og til tiden til patienter i hele. Vi arbejder løbende på at optimere vores processer, nedbringe leadtime og brug af ressourcer ved hjælp af diverse LEAN værktøjer

Jobbet
Teamets primære ansvar består i at forberede pakkemateriale til pakning (herunder bl.a. print af etiketter) og pakke produkter til kliniske studier. Pakningen foregår både manuelt og på en automatiseret pakkelinie. Dette job er dog udelukkende til den manuelle pakning.

Du vil indgå i et team med meget dedikerede medarbejdere, og som består af 6 pakkeriteknikere, 2 håndværkere, 1 planlægger og 25 operatører.

Som pakkeriassistent er du primært ansvarlig for manuel pakning og etikettering af vials, penfills, og dumaer til kliniske studier, men din rolle kan udvides til fremtagning af produkter fra lageret, kontrolopgaver, samt udfærdigelse af batchdokumentation. Du kan også forvente at deltage i Lean aktiviteter samt løse mange ad hoc opgaver i relation til pakkeprocessen.

Jobbet er et dagholdsjob og er midlertidigt frem til december 2015.

Kvalifikationer
Der kan være flere uddannelsesmæssige tilgange til jobbet, men vi forestiller os, at du har en relevant baggrund, der matcher udfordringerne i jobbet, gerne suppleret med en uddannelse på operatørniveau som f.eks. industrioperatør. Det er en fordel, hvis du har erfaring med og forståelse for arbejdsgangene ved pakkeordrer til kliniske studier og kendskab til farmaceutiske produkter, arbejdsprocesser og dokumentationskrav.

Jobbet kræver, at du kan håndtere komplekse pakkeopgaver, samt at du har et kvalitetsmindset, der sikrer, at du aldrig går på kompromis med kvaliteten af det, du leverer. Dit arbejde kommer til at foregå i samarbejde med mange forskellige medarbejdere og du skal derfor have gode samarbejds og kommunikationsevner, samt være en udpræget team-player.

Da vi tit arbejder under tidspres er det vigtigt, at du kan holde hovedet koldt i pressede situationer. Selvom du indgår i et team, er det vigtigt, at du kan arbejde selvstændigt, og at du har en positiv og konstruktiv tilgang til opgaveløsning og forandringer. Kendskab til GMP og LEAN er en fordel, men ikke et krav. Sidst men ikke mindst forventer vi, at du er fleksibel, positiv og har et godt humør.

Ansættelse ønskes snarest muligt.

Fast dagholdsstilling til medarbejdere med min. 3 års anciennitet eller medarbejdere, der har været via revalideringsforløb

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Martin Baunø Nielsen på +45 3075 1760

Ansøgningsfrist
11. maj 2014

Danmark - Måløv Produktions operatør
22-Apr-2014 Professional
Er procesforbedringer lige dig? Og har du lyst til at arbejde med aseptisk produktion hos verdens førende producent af insulin? Så har vi det helt rigtige job til dig som produktionsingeniør til processupport i...

Professional

  • Produktion
  • Danmark - Bagsværd

Er procesforbedringer lige dig? Og har du lyst til at arbejde med aseptisk produktion hos verdens førende producent af insulin? Så har vi det helt rigtige job til dig som produktionsingeniør til processupport i Bagsværd. Grib muligheden for en karriere med gode udviklingsmuligheder, en dynamisk hverdag og en stor kontaktflade i en international virksomhed.

Om afdelingen
Du bliver en del en afdeling som sikrer drift og frigivelse fra én af vore fyldelinjer i Bagsværd. Som en del af Proces Support & Teknisk Support får du ca. 10 kolleger, som tæller både ingeniører, farmaceuter, kemikere og supportere. Tilsammen har vi ansvaret for den daglige driftssupport til fyldelinjen.

Jobbet
Din fornemmeste opgave bliver at yde daglig support til driften af vores aseptiske fyldeproces så vi opretholder en stabil og kontinuerlig produktion. I tæt samarbejde med operatører, supportere, teknisk support og QA løser du en bred vifte af opgaver lige fra procesforbedringer, valideringer og afvigelsessager. Når der opstår udfordringer i vores produktion, er det dig, der sikrer overblikket, så problemerne kan løses hurtigt og effektivt. Du spiller således en nøglerolle i arbejdet med at sikre drift og frigivelse af produkterne – og du, at afdelingen altid er i compliance med gældende lovkrav. Deltagelse i større og mindre optimerings- og standardiseringsprojekter bliver også en del af din nye hverdag.

Kvalifikationer
Vi forestiller os, at du har en relevant akademisk uddannelse såsom produktions-, kemi-, maskin- eller procesingeniør, farmaceut, biolog, mikrobiolog eller lignede. Uanset din baggrund skal du have viden om

GMP – gerne relateret til aseptisk produktion. Har du tilmed erfaring fra farmaceutisk produktion (herunder FDA) samt kendskab til valideringsarbejde og LEAN, er det absolut et plus. Som person er du en problemknuser, og du trives i en dynamisk hverdag, hvor din evne til at træffe beslutninger er helt essentiel. Da kvalitet og præcision er afgørende i lægemiddelindustrien, er det også vigtigt, at du er kvalitetsbevidst og har lyst til og erfaring med skriftlig dokumentation. For at få succes i stillingen er fortrolighed med IT og evnen til at sætte dig ind i nye systemer alfa og omega. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så er du meget velkommen til at kontakte Søren Dam på + 45 3079 1815.

Ansøgningsfrist
11. maj 2014

Danmark - Bagsværd Produktion
22-Apr-2014 Rensningstekniker til API finrensningspilotanlæg i Bagsværd
Har du lyst til en alsidig dag, hvor du bruger dine kompetencer ift. proceskendskab, procesafvikling, udstyrskendskab samt GMP-dokumentation på et højt niveau? Så har vi stillingen til dig i CMC API Development...

Rensningstekniker til API finrensningspilotanlæg i Bagsværd

  • Forskning og Udvikling
  • Danmark - Bagsværd

Har du lyst til en alsidig dag, hvor du bruger dine kompetencer ift. proceskendskab, procesafvikling, udstyrskendskab samt GMP-dokumentation på et højt niveau? Så har vi stillingen til dig i CMC API Development, Downstream Pilot Plants, bygning 1T i Bagsværd hvor vi søger 1 selvstændig og erfaren tekniker med flair for både proces og papirarbejde.

Om afdelingen
Den ledige stilling er i Multikolonne teamet i Bagsværd, som er en del af en større afdeling med ca. 70 ansatte fordelt i 4 oprensningspilotanlæg på tværs af Bagsværd og Gentofte. Teamet har 8 teknikere samt 4 kemikere. Fra 1. januar 2015 er det planen, at alle teknikere skal på holddrift, dvs. jf. turnusplan indeholdende aften- og weekendvagter.

Kerneydelsen er levering af API til de kliniske studier, hvilket produceres kampagnevis, dvs. anlægget håndterer forskellige processer og proteiner. Sidste år havde vi eks. 6 forskellige produkter igennem anlægget. Vi har naturligvis en del rutineopgaver, men i og med vi er en del af udviklingen, er der sjældent 2 dage, der er ens.

Jobbet
Vi tilbyder et spændende og afvekslende job i et åbent og dynamisk arbejdsmiljø med god mulighed for faglig og personlig udvikling.

Arbejdsopgaverne vil være relateret til procesafviklingen i anlægget med fokus på præparativ oprensning, dvs. kemiske modifikationstrin, søjleoprensning, fældning, centrifugering og frysetørring. Du vil også skulle deltage i andre af teamets opgaver i forbindelse med løbende kontrol af bl.a. udstyr, råvarehåndtering, miljøprøver mv.

I afdelingen arbejder vi med cLEAN og stræber efter at forenkle samt gøre vore arbejdsprocesser værdiskabende. Det forventes derfor, at du har en konstruktiv tilgang til opgaverne, bidrager og er i stand til at føre forbedringer ud i livet. Du arbejder systematisk med problemløsning og er opsøgende ift. at tale med data.

Kvalifikationer
Du er uddannet kemotekniker, procesteknolog, levnedsmiddeltekniker eller lignende, og det er en stor fordel at du har praktisk oprensningserfaring i laboratorie-/pilotskala eller fra produktionen dvs. erfaring med søjlekromatografi, GMP samt proces kontrolsystemer (Sattline og Unicorn) eller som minimum med tilsvarende styresystemer.

Du motiveres af at sikre stabile processer og går foran, når der er udfordringer med udstyr eller proces, så produktionsplanerne overholdes, og vi dermed kan levere rette mængder til rette tid og i rette kvalitet.

Evne til samarbejde og kommunikation er en nødvendighed, da opgaverne bliver løst i fællesskab, og samtidig forventes det, at du tager ansvar og kan løfte opgaver selvstændigt.

Vi lægger vægt på, at du har et godt humør og kan lide at tage fat i opgaverne, også når de ikke bliver lagt tilrette foran dig.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Teamleder Charlotte Hother le Fevre på tlf. +45 3075 1148.

Ansøgningsfrist
2. maj 2014

Danmark - Bagsværd Forskning og Udvikling
22-Apr-2014 Industritekniker - med speciale indenfor plast
Vi har brug for dit engagement og dine kompetencer i vores støbeafdeling, for at vedligeholde og optimere vores produktions linjer til at være blandt de allerbedste i verden. Om afdelingen...

Industritekniker - med speciale indenfor plast

  • Produktion
  • Danmark - Hillerød

Vi har brug for dit engagement og dine kompetencer i vores støbeafdeling, for at vedligeholde og optimere vores produktions linjer til at være blandt de allerbedste i verden.

Om afdelingen
Novo Nordisks DMS Production er placeret i Hillerød. Her arbejder 90 engagerede medarbejdere, som er ansvarlige for alle faser af produktionen fra plastgranulat til den præmonteret insulinpen FlexTouch ® og FlexPen ®. Du bliver del af en afdeling, hvor LEAN står højt på dagsordenen Vi stræber efter ambitiøse mål og optimere løbende på vores arbejdsgange og processer. Vi har samtidig stort fokus på trivsel og udvikling af medarbejdere.

Jobbet
Du vil indgå i vores Plast-Tech. Support team, som i dag består af 16 Plastteknikere, og 9 Automatikteknikere.

Vi varetager reparationer og vedligeholdelse på vores forme med tilhørende ekstraudstyr. Vi arbejder på rulleskift og dækker produktionen 24/7.

Vi er en afdeling i rivende udvikling, hvor nyt udstyr er en del af hverdagen, og foruden daglig vedligehold og fejlretning, kommer du til at medvirke i optimeringsprojekter og daglig systematisk problemløsning.

Udfordringerne er mange, derfor har vi positive forventninger til dig.

Så har du mod og lyst til at medvirke til løsning af tekniske problemstillinger og forbedringer både i samarbejde med teamet - men også selvstændigt - Så kan vi tilbyde dig et dynamisk produktionsmiljø, gode kollegaer samt træning i vore linjer, så vi i fællesskab når i mål.

Stillingen er kategoriseret som F3

Kvalifikationer
Vi forestiller os, at du har en faglig uddannelse som industritekniker, værktøjsmager, maskinarbejder, eller anden relevant baggrund. Vi ser gerne du har flere års indgående kendskab til plastsprøjtestøbning og optimering af forme og ekstraudstyr.

Det er nødvendigt, at du er vant til at anvende IT, da IT danner grundlag for en stor del af vores processer, og arbejdsgange. Det er desuden vigtigt, at du har stærk kvalitetsforståelse, da vi arbejder indenfor ISO/GMP.

Som person har du gode samarbejdsevner og et opsøgende service mind-set. Du er fleksibel med stor ansvarsfølelse, og parat til en hverdag med variation i opgaverne. Du er en holdspiller og en god kollega, der altid er parat til at give en hånd med.

Endvidere lægger vi vægt på, at du har en god ordenssans samt et godt humør.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Grith Albrecht på + 45 3075 8559.

Ansøgningsfrist
30. april 2014

Danmark - Hillerød Produktion
16-Apr-2014 QC Supporter
Har du erfaring med GMP og kan du håndtere så forskelligartede opgaver som projektledelse, afvigelseshåndtering, problemløsning og dokumentskrivning? Trives du desuden med at arbejde med kvalitetskontrol? Hvis ...

QC Supporter

  • Produktion
  • Danmark - Bagsværd

Har du erfaring med GMP og kan du håndtere så forskelligartede opgaver som projektledelse, afvigelseshåndtering, problemløsning og dokumentskrivning? Trives du desuden med at arbejde med kvalitetskontrol? Hvis svaret er ja, kan du måske være vores nye QC Supporter.

Om afdelingen
Du vil blive en del af QC Packaging Materials i Bagsværd. Vi er ansvarlige for kvalitetskontrol af trykte- og primære pakkematerialer til produktionsafdelinger i Danmark og resten af verden. Vores fokus er at levere høj kvalitet til de aftalte deadlines – hver gang. I dag er vi 41 dedikerede medarbejdere i to teams, og den aktuelle stilling ligger i QC Printed Pack teamet.

Jobbet
Dine overordnede mål i jobbet er at sikre compliance og nå deadlines for afdelingens opgaver indenfor både kvalitet og levering af trykte pakkematerialer. Du koordinerer og er operationelt ansvarlig for projekter, hvor du definerer milestones og sikrer at vi når de aftalte deadlines. Du er ansvarlig for forbedringsprojekter i afdelingen og deltager i tværorganisatoriske grupper. Du får en vigtig rolle i at supportere QC-assistenterne i deres daglige arbejde og i at sikre at vores måleudstyr lever op til gældende krav for området. Derudover er håndtering af afvigelser og dokumentskrivning andre vigtige opgaver. Generelt kan du se frem til et spændende, alsidigt og udfordrende job.

Kvalifikationer
Du har en akademisk uddannelse sandsynligvis indenfor naturvidenskab. Du har erfaring fra GMP, og måske tilmed praktisk erfaring med kvalitetskontrol. Derudover er du interesseret i kalibrering og validering af IT-baserede kvalitetskontrolsystemer. Hvis du ikke allerede har praktisk erfaring med LEAN er du motiveret for at lære det. Du er struktureret og analytisk, kan identificere årsager og efterfølgende tilpasse metoder/procedurer/processer for at forebygge at problemet vender tilbage. Du trives med at have kontakt til mange mennesker, og du bruger dine gode kommunikationsevner til at skabe gode relationer til interessenter. For at lykkes i jobbet er det vigtigt, at du kan arbejde selvstændigt og planlægge dine egne opgaver. Du taler og skriver flydende dansk og du mestrer engelsk på professionelt niveau.

Hos Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Michael Lange +45 3079 1995.

Ansøgningsfrist
4. maj 2014

Danmark - Bagsværd Produktion
15-Apr-2014 Akademiker til IM2 Fermentation Support, Kalundborg
Brænder du for et job i et travlt produktionsmiljø? Kan du lide at lave grundig og systematisk problemløsning på baggrund af data, ved brug af LEAN-værktøjer, og trives du med at arbejde på tværs af faggrænser?...

Akademiker til IM2 Fermentation Support, Kalundborg

  • Produktion
  • Danmark - Kalundborg

Brænder du for et job i et travlt produktionsmiljø? Kan du lide at lave grundig og systematisk problemløsning på baggrund af data, ved brug af LEAN-værktøjer, og trives du med at arbejde på tværs af faggrænser? Så er du måske den akademiker vi søger til vores gæringssupport team.

Om afdelingen
Vil du være med til at sikre kvaliteten af insulinprodukter på de allerførste trin i produktionsprocessen? Så er du måske vores nye kollega i afdelingen Fermentation, hvor vi har ansvaret for både gæringsproces, utilitysystemer og produktionsudstyr. Dit team består af supportere med både tekniks og akademisk baggrund, som konstant overvåger procesafvikling, gæringstanke og de fysiske anlæg i fabrikken – Insulin Manufacturing II (IM2) i Kalundborg. Glæd dig til et job, hvor du er med til at gøre en forskel for produktionen af bl.a. human insulin og moderne insuliner.

Jobbet
Sammen med teamet får du ansvaret for at sikre, at produktkvaliteten er i orden i henhold til gældende myndighedskrav. Dine primære opgaver bliver bl.a. at overvåge og søge fejlårsager og trends i processen via vores it-systemer, ligesom du udarbejder SOPs, e-logs, reviews og afvigelsesrapporter. Du opretter ændringssager og sparrer med dine kolleger i vedligeholdsafdelingen. Desuden kommer du til at deltage i og drive mindre og større projekter med henblik på at optimere vores udstyr og processer. Vi arbejder indgående med Lean, og på vores daglige tavlemøder bidrager du med ideer til at sætte struktur på vores problemløsning og igangsætte f.eks. workshops. Du kan se frem til en stilling, hvor du får rig mulighed for at udvikle dine personlige og faglige kompetencer og sætte dit præg på samarbejdet i afdelingen. Jobbet indebærer specifikt ansvaret for vores vand- og dampanlæg. Det er således dit ansvar at følge op på kvaliteten af vand og damp, som har stor fokus i afdelingen, og foretage årlige afrapporteringer af dette. Som ansvarlig for vand/damp vil du endvidere blive en del af procesgruppe på tværs af Diabetes API, hvor du vidensdeler og harmoniserer med øvrige fabrikker i DAPI.

Kvalifikationer
Din baggrund er en relevant akademisk uddannelse og gerne erfaring fra kemisk, farmaceutisk eller fødevareproduktion. Du har god forståelse for samspillet mellem proces og udstyr og kendskab til GMP eller et lignende kvalitetssystem. Med andre ord er du yderst kvalitetsbevidst, og har du erfaring med optimering af såvel produktion som administrative processer, er det en fordel. Dine kolleger eller studiekammerater kender dig som en engageret og positiv person, der er meget bevidst om sit ansvar. Du kan både arbejde selvstændigt og indgå i tæt samarbejde – også selvom det er på tværs af team og faggrænser. Endelig interesserer du dig for Lean, og du er positivt indstillet over for forandringer, da du er god til at se muligheder frem for begrænsninger.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Thomas Neergaard på + 45 3075 3994

Ansøgningsfrist
4. maj 2014

Danmark - Kalundborg Produktion
15-Apr-2014 Studentermedhjælper
Studentermedhjælper til Steno Center for Sundhedsfremme Vil du være med til at udvikle nye tilgange til at forebygge diabetes? - og har du lyst til at være en del af et konkret forsknings- og udviklingsprojekt...

Studentermedhjælper

  • Studerende
  • Danmark - Gentofte

Studentermedhjælper til Steno Center for Sundhedsfremme

Vil du være med til at udvikle nye tilgange til at forebygge diabetes? - og har du lyst til at være en del af et konkret forsknings- og udviklingsprojekt om sundhedsfremme? Så skal du måske være vores studentermedhjælper?

Steno Center for Sundhedsfremme er et forskningscenter, som udvikler ny viden, metoder og tilgange til sundhedsprofessionelle og andre aktører, som kan skabe bæredygtig social forandring til fremme af folkesundheden i relation til diabetes. Centeret integrerer social- og humanvidenskabelig forskning for at skabe nye tilgange på et område, som trænger til at blive videnskabeligt fornyet. Centerets ambition er at udvikle et nationalt og internation¬alt kraftcenter med fokus på social forandring.

SoL Odsherred – Sundhed og Lokalsamfund

Steno Center for Sundhedsfremme fokuserer på forebyggelse af type 2 diabetes med udgangspunkt i børnefamilier og lokalsamfund. Inspireret af supersetting konceptet, som arbejder med sundhedsfremme baseret på synergier mellem forskellige arenaer (settings), søger SoL at fremme sundhed og trivsel blandt familier med små børn i tre lokalsamfund i Odsherred Kommune. Projektet implementeres i samarbejde med Aalborg Universitet og Forskningscenter for Forebyggelse og Sundhed i Glostrup.

Stillingen

På Steno Center for Sundhedsfremme, Steno Diabetes Center, søger vi en studentermedhjælper til SoL Odsherred projektet. Arbejdet vil omfatte forskellige opgaver, som litteratursøgning, transskription, mødeforberedelse og arbejde med videnskabelige manuskripter. Der vil dog i den første tid være hovedvægt på gennemførelsen af semi-strukturerde interviews i forbindelse med en interessent-analyse i Odsherred Kommune. Ansættelsen er i gennemsnit tre dage om ugen i Forebyggelsesgruppen ved Steno Center for Sundhedsfremme og vil vare til udgangen af 2014. Der må påregnes en øget arbejdsindsats i de første måneder. Dele af arbejdet vil foregå i Odsherred Kommune.

Din profil

• Du har en bachelor i et relevant fag, fx folkesundhedsvidenskab, sundhedsfremme, pædagogik, sociologi, antropologi, idræt eller psykologi.

• Du har solid erfaring med brug af kvalitative metoder herunder interviews.

• Du er dygtig, ambitiøs, motiveret, selvstændig, kreativ, engageret, resultatorienteret og en god kollega.

• Du har faglig og menneskelig modenhed og kan både arbejde selvstændigt og i et tæt samarbejde i en tværfaglig gruppe, hvor en positiv indstilling og humoristisk sans er afgørende.

• Du er tolerant og kan kommunikere med folk med forskellig baggrund.

• Du mestrer til fulde dansk og engelsk i skrift og tale.

Det er fordel, hvis du har erfaring med at:

• arbejde på forskningsprojekter.

• arbejde med feltarbejde i institutioner.

• arbejde i tværfaglige miljøer.

• arbejde med børn, familier og sundhedsfremme.

Ansøgning

Din ansøgning, på dansk eller engelsk, skal indeholde:

• Din motivation og baggrund for at søge stillingen (max 1 side)

• CV (max 2 sider)

Ansøgningen sendes elektronisk senest torsdag 1. maj 2014, kl. 12.00. Stillingen ønskes besat snarest muligt.

Kontakt

Yderligere information fås fra Paul Bloch (50926617).

Om Steno

Steno Diabetes Center er en af verdens førende institutioner inden for diabetesbehandling og forebyggelse. Steno ejes af Novo Nordisk A/S og er en 'not for profit' virksomhed, der arbejder i partnerskab med det danske sundhedssystem. Steno står for behandlingen af ca. 5.600 mennesker med diabetes. For yderligere oplysninger, se www.steno.dk.

Danmark - Gentofte Studerende
15-Apr-2014 Kvalificerings og- valideringsekspert til strategisk vigtig satsning
Vil du være en del af et innovativt produktionsmiljø, hvor vi pakker Novo Nordisks hæmofili-produkter og aldrig går på kompromis med kvalitet? Har du solid erfaring med kvalificering af udstyr og /eller valider...

Kvalificerings og- valideringsekspert til strategisk vigtig satsning

  • Produktion
  • Danmark - Kalundborg

Vil du være en del af et innovativt produktionsmiljø, hvor vi pakker Novo Nordisks hæmofili-produkter og aldrig går på kompromis med kvalitet? Har du solid erfaring med kvalificering af udstyr og /eller validering af processer på brugersiden fra medicinalbranchen? Og er du klar til en ekspertrolle, hvor du sætter din GMP viden helt i front til gavn for kolleger og patienter over hele verden? Så kan du meget vel være vores nye Kvalificerings- og proces supporter.

Biopharms nye pakkeri er en strategisk vigtig satsning, der skal sikre den fremtidige kapacitet til at pakke Novo Nordisks hæmofili-produkter samt GlucaGen® Hypokit. Det giver et dynamisk arbejdsmiljø, hvor vi på samme tid skal sikre stabile leverancer af livsvigtig medicin til vores kunder, håndtere forberedelsen af en ny pakkelinie samt støtte og udføre flere projekter i afdelingen.

Om afdelingen
Afdelingen i Biopharm, Finished Products består pt. af ca. 60 dygtige medarbejdere, der alle beskæftiger sig med pakning af NovoSeven® og NovoEight® og på sigt flere hæmofiliprodukter og GlucaGen® Hypokit. Afdelingen er relativ ny og forventes ligeledes at vokse betragteligt over de kommende år. Afdelingen er opdelt i tre teams; et produktions team, et proces support team og et teknisk support team. Du vil indgå i proces support teamet, hvor dine kommende kolleger består af akademikere og laboranter.

Jobbet
I Biopharm lægger vi vægt på, at alle tager et personligt ansvar for kvalitet, opgaver og hinanden. Vi sætter ambitiøse mål, samtidig med at vi fokuserer på stabil leverance til vores kunder. Din primære opgave er at være overordnet ansvarlig på bruger siden, når processerne skal valideres samt sikre kvalificering af vores udstyr. Både ved revalideringer og efterhånden som vi bygger vores produktion op.

Du vil fungere som afdelingens valideringsekspert ved inspektioner og audits. En del af dit arbejde vil også bestå i support til produktionen, udarbejdelse af afvigelser og frigivelse af vores produkter. Din arbejdsdag vil således blive afvekslende og til tider hektisk, da driften af vores fuldautomatiserede pakkelinje er essentiel for gennemførelse af produktionen. Arbejdet vil foregå i tæt dialog med mange medarbejdergrupper både i og udenfor afdelingen. Det betyder, at vi stiller lige store krav til selvstændighed og det at være en god teamplayer.

Kvalifikationer
Til tiltrædelse snarest søger vi en kollega, der har en solid baggrund indenfor kvalificering og/eller validering. Den ideelle kandidat har minimum 5 års erfaring indenfor færdigvareproduktion af medico- eller medicinalprodukter og en stor og dokumenteret forståelse for GMP. Du har en relevant uddannelsesmæssig baggrund som farmaceut, produktions-, kemi- eller maskiningeniør.

Du er en stærk kommunikator, der bliver lyttet til, når vi taler kvalificering, og er rigtig god til at formidle denne viden til andre. Du er vant til at arbejde selvstændigt, tage ansvar og finde løsninger i selv pressede situationer. Samtidig sikrer du involvering og ejerskab blandt dine kolleger, og er god til at etablere samarbejde på tværs af faggrænser. Du er åben og ærlig, og i stand til at give og modtage konstruktiv feedback. Vi arbejder i en GMP reguleret virksomhed, hvorfor du lægger vægt på detalje, struktur og kvalitet i dit arbejde.

Da Novo Nordisk A/S er en international virksomhed, er det et krav, at du behersker engelsk og dansk, såvel mundtligt som skriftligt.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Vi giver vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Nanna-Freja Riis Larsen på + 45 3079 1736.

Ansøgningsfrist
28. april 2014

Danmark - Kalundborg Produktion
15-Apr-2014 Kvalitetsassistent til Pilot Plant
Her er muligheden for at bruge din viden inden for GMP og kvalitetssystemer til at hjælpe Chemical Supply Pilot udvikle og fremstille næste generations lægemidler. Om afdelingen...

Kvalitetsassistent til Pilot Plant

  • Kvalitetssikring
  • Danmark - Bagsværd

Her er muligheden for at bruge din viden inden for GMP og kvalitetssystemer til at hjælpe Chemical Supply Pilot udvikle og fremstille næste generations lægemidler.

Om afdelingen
Chemical Development er vi 40 medarbejdere, som er organiseret i 3 teams og geografisk placeret i både Måløv og Bagsværd. Vi er ansvarlige for udvikling og opskalering af kemiske processer til support af til prækliniske og kliniske studier. Afdelingen dækker over en bred vifte af procesteknologier fra klassisk organisk syntese over fastfase syntese til kromatografisk oprensning. I teamet Chemical Supply Pilot er vi 17 kollegaer der sammen er ansvarlige for afvikling af pilotproduktioner, indsamling af procesdata samt optimering af fremstillingsprocesserne.

Jobbet
Som QMS assistent i afdelings pilot team, Chemical Supply Pilot, bliver du involveret i den daglige support til GMP produktion af API og mellemprodukter. Du vil få en bred vifte af ansvarsområder og opgaver i forbindelse med den daglige support.

Dit primære ansvarsområde som QMS assistent vil være det daglige ansvar for kvalitets-sikringsarbejdet, dvs. ansvarlig for at planlægge, opbygge og monitorere kvalitetssystemet i afdelingen. Endvidere har QMS assistenten ansvaret for at vedligeholde og effektivisere afdelingens kvalitetssystem og sammen med andre QMS repræsentanter være med til at vedligeholde og effektivisere områdets kvalitetssikringssystem.

I det daglige samarbejder du med en lang række af vores kollegaer, for at sikre compliance af processer og udstyr. Du er erfaren i brugen af IT systemer der understøtter den daglige GMP drift ift. den supporterende del, som dokumentation og kvalitet. Du er kvalitetsbevidst og en person der trives med opgaver som er en blanding af foranderlig og rutinemæssig karakter.

Kvalifikationer
Du har flere års erfaring med kvalitets arbejde inden for den farmaceutiske industri og har en teknisk baggrund (procesteknolog, farmakonom, laborant eller tilsvarende). Du er velorganiseret og trives med at der er orden og struktur i dokumentation og systemer.

Du har med fordel kendskab til de IT systemer der benyttes til kvalitetssikring inden for NovoNordisk (IsoTrain/QBIQ, LIMS, Omnirim mm) samt gerne kendskab til miljømonitorering af klassificerede områder.

På det personlige plan trives du med en høj grad af fleksibilitet – og med din evne til at omstille dig, befinder du dig rigtig godt i en stilling, hvor dagene ikke ligner hinanden. Du er struktureret, en god planlægger og har stort fokus på kvalitet i dit arbejde. Samtidig sætter du pris på en uformel tone og tæt samarbejde i teamet. Du er engageret, tager initiativ og søger selv udfordringer, du har et ”can do mind-set”.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Henrik Svane på + 45 3075 5695 eller Thomas Pittelkow på + 45 3079 3936

Ansøgningsfrist
9. maj 2014

Danmark - Bagsværd Kvalitetssikring
15-Apr-2014 Teamleder
Er du klar til at lede og motivere et team af højt kvalificerede kollegaer i et team, der arbejder med support til Biopharm AP produktioner i Gentofte og Kalundborg og sikre konsistens imellem både nye og marke...

Teamleder

  • Produktion
  • Danmark - Gentofte

Er du klar til at lede og motivere et team af højt kvalificerede kollegaer i et team, der arbejder med support til Biopharm AP produktioner i Gentofte og Kalundborg og sikre konsistens imellem både nye og markedsførte produkter? Kan du sætte en klar retning for dit team og fungere som en inspirerende sparringspartner for dine medarbejdere? Kan du bevare roen og prioritere opgaver i et dynamisk og hektisk miljø? Så har vi en stor mulighed for dig i Biopharm AP support.

Om afdelingen
I Biopharm AP Support er vi mere end 50 kompetente kolleger, der yder support til de forskellige AP produktionsprocesser inden for Biopharms portefølje bestående af hæmofiliprodukter, Norditropin ® og GlucaGen ®. Afdelingen fungerer som et bindeled mellem udvikling og produktion, så vi har fingeren på pulsen i alle de spændende nye og markedsførte produkter i Biopharms pipeline. Afdelingen er i dag opdelt i to teams, men da afdelingen fortsat vokser, etablerer vi nu et tredje team med ansvar for en kombination af nye og markedsførte produkter. Dit job bliver at lede dette nye team og være en del af den daglige ledelse i afdelingen. Afdelingen er placeret i Gentofte.

Jobbet
Som teamleder i det nye team, kommer du til at lede et team på ca. 13-15 fagligt dygtige og kompetente medarbejdere. De vigtigste opgaver bliver at sikre koordinering og prioritering af support til AP produktionerne, håndtering og koordinering af produkt-og procesorienterede opgaver samt sikre svar på spørgsmål fra myndighederne.

Nøglen til succes ligger i din evne til at en være en inspirerende, coachende og motiverende leder, der på samme tid, kan håndtere administrative opgaver og kontakt til mange interessenter i en kompleks organisation. For at opnå dette, skal du lede dine medarbejdere på daglig basis, og sørge for, at vi har de rigtige ressourcer i teamet.

Du spiller også en væsentlig rolle i løbende at skabe forbedringer gennem brugen af LEAN, så vi hele tiden optimerer vores arbejdsprocesser. Det gør du bl.a. gennem målstyring, systematisk problemløsning og opfølgning på efterlevelse af standarder. Du kan se frem til et miljø, hvor der hele tiden sker noget, og hvor du hver dag skal træffe vigtige beslutninger i forhold til levering, prioritering og skarpe deadlines.

Kvalifikationer
Du har en baggrund, som farmaceut, ingeniør eller tilsvarende, suppleret med solid erfaring i farmaceutisk produktion, der arbejder i overensstemmelse med GMP/ISO. Du har en naturlig interesse i personaleledelse og dit CV afspejler minimum 5 år ledelsesmæssig erfaring.

Du har en god sans for planlægning, arbejder systematisk og struktureret og er i stand til at opretholde det generelle overblik. Det er vigtigt, at du kender værdien af at skabe tillid og respekt fra kolleger og medarbejdere og ved, hvordan man kan motiverer sine medarbejdere i en travl og skiftende hverdag. Du har gode kommunikationsevner på dansk og engelsk. Du er i stand til at dele viden på ethvert organisatorisk niveau, og med din udadvendte og proaktive indstilling kan du nemt oprette et netværk på tværs af organisationen. Endelig har du et vågent øje for kvalitet og formår at prioritere dit arbejde til at opfylde enhver deadline.

Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

I Novo Nordisk, Biopharmaceuticals, bruger vi vores kompetencer, engagement og ambition om at hjælpe mennesker med hæmofili og væksthormonmangel og ændre deres liv. Ved at arbejde sammen med os, vil du have mulighed for at gøre det samme i et globalt erhvervsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Martin Arendt Petersen på + 45 3079 8228

Ansøgningsfrist
30. april 2014

Danmark - Gentofte Produktion
15-Apr-2014 Processupporter
Brænder du for aseptisk produktion og vil du arbejde hos verdens førende insulinproducent? Vi mangler en dygtig kollega til at supportere vores aseptiske fyldeproduktion. Grib muligheden for et job med masser a...

Processupporter

  • Produktion
  • Danmark - Bagsværd

Brænder du for aseptisk produktion og vil du arbejde hos verdens førende insulinproducent? Vi mangler en dygtig kollega til at supportere vores aseptiske fyldeproduktion. Grib muligheden for et job med masser af udvikling, en afvekslende hverdag med stor indflydelse og ansvar i en international virksomhed.

Om afdelingen
I afdelingen er vi ca. 70 medarbejdere, hvoraf vi er 10 processupportere, som dagligt yder support til en af vores fyldelinjer. Afdelingen består af operatører, teknikkere, ingeniører, farmaceuter og kemikere som alle arbejder tæt sammen og på tværs af flere afdelinger.

Vores fornemmeste opgave er at sikre vores produktion køre 24/7 og altid levere insulin til vores kunder i rette kvalitet og til rette tid.

Jobbet
Din vigtigste opgave bliver at yde en god og effektiv support så vi sikre en stabil drift af vores aseptiske fyldeproces. Undervejs vil du skulle bidrage til at løse en bred vifte af opgaver lige fra procesforbedringer, valideringer, systematisk problemløsning og afvigelsessager.

Når der opstår udfordringer i vores produktion, er det dig, der sikrer overblikket, så problemerne kan løses effektivt og korrekt. Du spiller således en nøglerolle i arbejdet med at sikre driften og samtidig være garant for frigivelse af vores produkter.

En stor del af dit arbejde vil foregå i samarbejde med andre hvor sparring og udveksling af ideer og viden vil være essentiel for opgaveløsningen. Du vil også skulle byde ind med viden og evner når det kommer til compliance og kvalitet så vi altid lever op til gældende myndighedskrav.

Som Aseptisk Processupporter kan vi tilbyde dig et udfordrende og innovativt miljø med gode muligheder for både personlig og faglig kompetence udvikling. Du vil opleve et godt sammenhold og et fælles ønske om at sørger for vores patienter for deres medicin.

Kvalifikationer
Du har en relevant naturvidenskabelig uddannelse som produktions-, miljøkemi- eller kemiingeniør, cand. scient el. lign. Du har et stort indblik i proteinkemi og aseptisk produktion. Desuden har du et godt kendskab til GMP/ISO reglerne og erfaring med audits.

Du besidder flere års erfaring fra lignende stilling, og det falder dig naturligt at tage ansvar, sætte retning og træffe beslutninger for dig selv og dine kollegaer i det daglige arbejde.

Du har evt. før været projektleder, haft ansvar for dele af produktionsprocesser eller andre tværgående processer, som gør, at du har et naturligt overblik og drive. Derudover har du solidt kendskab til LEAN, og det er en selvfølge for dig at bruge problemløsningsværktøjer i dit daglige arbejde. Samtidig skal du have lyst til at facilitere, udfordre og hjælpe dine kollegaer med brugen af disse værktøjer i hverdagen, så vi fortsat løfter vores høje niveau.

Du kommunikerer klart og tydeligt på både dansk og engelsk. Du er mål- og ansvarsbevidst og har viljen til at gå forrest både fagligt og i samarbejdet med alle faggrupper. Du er nysgerrig og udfordrende, og du tør tage styringen og danne dig et overblik ved f.eks. tværgående projekter og systematisk problemløsning. Ligeledes skal du kunne lære fra dig og være indstillet på indimellem at indtage en mentorrolle for andre processupportere eller operatører i fabrikken.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Jeanette Hejli Sørensen på + 45 3075 2412.

Ansøgningsfrist
15. maj 2014

Danmark - Bagsværd Produktion
14-Apr-2014 Kemiker
Kan du hjælpe os med at etablere og drive en moderne og professionel fyldefabrik? Så kan du blive en del af Novo Nordisk’s største investering i Danmark i mange år. Vi ser frem til at invitere dig ind i en proj...

Kemiker

  • Produktion
  • Danmark - Kalundborg

Kan du hjælpe os med at etablere og drive en moderne og professionel fyldefabrik? Så kan du blive en del af Novo Nordisk’s største investering i Danmark i mange år. Vi ser frem til at invitere dig ind i en projektorganisation, der består af fagligt dygtige, ambitiøse og målrettede medarbejdere.

Om afdelingen
I Biopharm-divisionen af Novo Nordisk har vi blandt andet ansvaret for at producere NovoSeven®, de kommende generationer af hæmofili-præparater, Glucagon og andre Biopharm produkter. Vi oplever en stigende efterspørgsel og har valgt at etablere en ny fabrik i Kalundborg for at sikre fyldning af vores produkter.

Afdelingen kommer til at bestå af lidt over 100 medarbejdere, som over de næste par år skal oplæres og trænes i vask og sterilisation, formulering, fyldning, frysetørring og inspektion af biofarmaceutiske produkter.

Jobbet
I jobbet som Fylde kemiker vil du komme til at samarbejde tæt med operatører, supportere og QA. Hovedvægten i projektfasen vil være at deltage i kvalificeringen af udstyret og processen, samt at sikre en glidende overgang fra projekt til produktion.Når der opstår udfordringer i vores projekt/produktion, er det dig, der sikrer overblikket, så problemerne kan løses hurtigt og effektivt.Deltagelse i større og mindre optimerings- og standardiseringsprojekter bliver også en del af din nye hverdag, samt deltagelse ved myndighedsinspektioner. Derudover deltager du aktivt i at yde daglig support til driften af vores aseptiske produktion. Du spiller således en nøglerolle i arbejdet med at sikre drift og frigivelse af produkterne – og så sikrer du, at afdelingen altid er i compliance med gældende lovkrav.

Kvalifikationer
Du er farmaceut, kemiingeniør eller lignende og har lyst til at udvikle dig i et farmaceutisk produktionsmiljø. Kendskab til mikrobiologi er et stort plus. Du har erfaring fra arbejdet i et GMP-reguleret miljø og forstår, hvad der er god adfærd i en aseptisk produktion. Samtidig kender du til LEAN-værktøjer og er i stand til at bruge det på et højt fagligt niveau.Dine formidlings og kommunikationsevner er i top, og du er en ørn til at samarbejde. Det falder dig også helt naturligt at skabe overblik, selvom du varetager mange forskellige opgaver på samme tid. Samtidig er du resultatorienteret, initiativrig, engageret, fleksibel og vant til at tage ansvar. Sidst, men ikke mindst, har du har en positiv indstilling og lyst til at være en nøgleperson i en stor afdeling. Du taler og skriver både dansk og engelsk flydende.

Site Kalundborg er en by i byen, kun godt en times kørsel fra København. Området er på 1.350.000 m2 med eget vejnet. Vi er 3.500 mennesker i alt fordelt på 16 fabrikker, og vi producerer bl.a. 50 % af verdens insulin. Site Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Anne-Mette Meldgaard på +45 3075 0190.

Ansøgningsfrist
11. maj 2014

Danmark - Kalundborg Produktion
14-Apr-2014 Senior QA med et projektorienteret fokus
Vil du være en del af et projektorienteret QA miljø, og have ansvar for kvaliteten i flere af vore store strategiske projekter? Er du klar til en ekspertrolle med markant ansvar, hvor du aldrig går på kompromis...

Senior QA med et projektorienteret fokus

  • Kvalitetssikring
  • Danmark - Kalundborg

Vil du være en del af et projektorienteret QA miljø, og have ansvar for kvaliteten i flere af vore store strategiske projekter? Er du klar til en ekspertrolle med markant ansvar, hvor du aldrig går på kompromis med kvalitet og compliance til gavn for kolleger og patienter over hele verden? Så grib chancen og søg jobbet som QA i Novo Nordisk´s største færdigvarefabrik i Kalundborg.

Om afdelingen
Du bliver en del af QA for Site Danmark (SDK) i Kalundborg, hvor vi tæller 40 dedikerede og engagerede medarbejdere som er fordelt på tre teams – et der varetager QA for aseptisk produktion, hvor vi skal udvide med en fyldelinje og to der varetager QA for montage- og pakke processer samt projekter. Sammen med 9 engagerede kolleger udgør du afdelingens QA med ansvar for kvaliteten i strategisk vigtige projekter både i produktion, IT og lager. Der bliver arbejdet i højt tempo med konstant fokus på compliance og kvalitet. Dette sker i tæt samarbejde med både interne og eksterne projektledere i SDK.

Jobbet
Du får rollen som den afgørende QA person, der med din høje faglighed og kvalitetsviden er med til at bygge kvalitet ind i processerne og udstyret. Du vil deltage i projekter – både store og små – hvor du igennem din viden og kompetencer skal tilsikre, at systemer og processer er i compliance med GMP reglerne. Du får en central rolle og vil skulle træffe afgørende beslutninger, når projekterne skal planlægges og gennemføres.

Foruden opgaver og udfordringer i de projekter, som du er QA på, vil du samtidig være ansvarlig for at QA godkende CR-sager, kvalificeringer, SOP’er og afvigelser relateret til den daglige drift. Du vil blive involveret i problemløsninger i samarbejde med produktionen.

Nogle af de store projekter du skal lykkes med er bl.a.: Revalidering af produktionslinjer, hvor alle montage og pakke linjer skal revalideres. Dette projekt løber i flere år og vil give dig god indsigt i validering. Desuden har vi grundet nye krav om stregkoder på produkter igangsat Serialiseringsprojektet, som varer til 2017. Og i år, på den kortere bane, er vi igang med etablering af ny fyldelinje i aseptisk område. Ved hver implementering skal vi igennem hele valideringsforløbet – fra A-Z.

Kvalifikationer
Du er uddannet farmaceut, ingeniør eller relevant cand.scient uddannelse, og dit cv afspejler minimum 4 års erfaring indenfor QA og/eller GMP produktion, hvor du har fået et bredt kendskab til GMP og farmaceutisk produktion. Derudover skal du kunne kommunikere på både dansk og engelsk – mundtligt så vel som skriftligt.

Vi kan tilbyde et job hvor du er den der samler trådene og udstikker kursen for dine samarbejdspartnere. Du får selvstændigt ansvar for at træffe de afgørende beslutninger. Vi tilbyder et positivt arbejdsmiljø med et ønske og vilje til at løse udfordringer og vi har en åben og ærlig dialog, som foregår i øjenhøjde med hinanden. Du deler gerne ud af dine gode råd og faglige argumenter.

Arbejdsdagene vil være alsidige – ikke to dage er ens, hvilket kræver høj grad af struktur, effektivitet og godt humør.

Du kan lære mere om Novo Nordisk Product Supply og arbejdet i QA ved at bruge linket www.novonordisk.com/careers/QA

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Jytte Holm Iversen på +45 3079 7767.

Ansøgningsfrist
27. april 2014

Danmark - Kalundborg Kvalitetssikring
11-Apr-2014 Laborant
Har du den viden og erfaring der skal til, for at skabe nyt og udvikle fremtidens diabetes produkter? Hvis ja, så har du muligheden for at spille en nøglerolle i CMC Diabetes Formulation Development i Måløv. So...

Laborant

  • Forskning og Udvikling
  • Danmark - Måløv

Har du den viden og erfaring der skal til, for at skabe nyt og udvikle fremtidens diabetes produkter? Hvis ja, så har du muligheden for at spille en nøglerolle i CMC Diabetes Formulation Development i Måløv. Som bindeledet mellem forskning og produktion, er vi ansvarlige for at udvikle subkutane injicerbare formuleringer og processer – hele vejen fra tidlig udvikling til fase III klinikstudier og registrering.

Om afdelingen
Afdeling CMC Diabetes Formulation Development, som er en del af R&D, er organiseret i to teams med i alt 30 personer. Afdelingen repræsenteres i projektgrupper på tværs af organisationen, hvor vi hele tiden bestræber os på at levere resultater af en høj kvalitet. Du vil blive en del af Team Diabetes Formulation Development I som er ansvarlig for formuleringsudvikling og procesudvikling, inklusiv stabilitet og dokumentation til kliniske studier.

Team Diabetes Formulation Development I består af 6 laboranter og 12 kemikere samt en teamleder. Vi er gode kollegaer, som sætter pris på samarbejde og teamwork.

Jobbet
Vi kan tilbyde et spændende og udfordrende arbejdsmiljø, hvor du kan bidrage ved at gøre en forskel. Dine opgaver bliver efter overordnede retningslinjer fra kemiker eller teamleder, selvstændigt at planlægge, fremstille, resultatvurdere og præsentere resultater fra udviklings- og stabilitetsforsøg. Du vil skulle planlægge, forberede og gennemføre præparation af aseptiske formuleringer til formuleringsudviklingsforsøg og stabilitetsstudier. Vi forventer, at du aktivt deltager i tilrettelæggelse af det daglige arbejde i laboratorierne således, at projekternes tidsplaner kan overholdes, samt at du er med til løbende at forbedre vores processer gennem cLEAN.

Kvalifikationer
Laboratorieteknisk basisuddannelse som f.eks. farmakonom, bioanalytiker, laborant eller kemotekniker. Du har praktisk faglig erfaring indenfor områderne proteinkemi og udvikling af sterile, farmaceutiske præparater suppleret med generel viden om GXP og anvendelse af IT software. Erfaring eller interesse for Excel vil være en fordel. Du er teamwork-orienteret med gode evner for samarbejde og du har lyst til at lære nyt. Du er omhyggelig, ferm til at organisere og planlægge dit arbejde, og du kan arbejde selvstændigt og ansvarsfuldt i laboratoriet. Som person er du positiv, fleksibel og har et godt humør.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Rozana Sten på + 45 3075 2472.

Ansøgningsfrist
27. april 2014.

Danmark - Måløv Forskning og Udvikling
11-Apr-2014 Automatik Specialist med højt drive og godt humør
Har du stor viden om drift af automatik systemer i et GMP-miljø? Og har du erfaring fra den farmaceutiske verden eller lignende reguleret industri? Vi søger en højt kvalificeret akademisk / teknisk profil med g...

Automatik Specialist med højt drive og godt humør

  • Produktion
  • Danmark - Kalundborg

Har du stor viden om drift af automatik systemer i et GMP-miljø? Og har du erfaring fra den farmaceutiske verden eller lignende reguleret industri? Vi søger en højt kvalificeret akademisk / teknisk profil med gode samarbejdsevner, der trives med at arbejde både operationelt og projektorienteret.

Om afdelingen
Biopharm AP’s fyldefabrik i Kalundborg er en ny aseptisk påfyldnings facilitet, der er ansvarlig for at formulering og fyldning af NovoSeven®, Glukagon® og andre biofarmaceutiske produkter.

IT & Automatik teamet er ansvarlig for drift og vedligeholdelse af facilitetens IT & Automatik udstyr, der dækker kontrolsystemer til formulering, påfyldning, frysetørring, capping og støtte processer. Vi er kendetegnet ved, at vi kender og tager vare på hinanden, og dermed bliver man som ny medarbejder meget hurtigt en del af fællesskabet. Vi lægger meget vægt på engagement, ansvarlighed, respekt og samarbejde samt en positiv, humoristisk omgangstone.

Jobbet
Vi er på udkig efter et nyt medlem til teamet, der kan spille en central rolle i at sikre den rette grad af compliance i de resterende valideringer, driftsfasen og i fremtidige projektvalideringer. Du vil sikkert også drive automatik relaterede opgraderings og forbedringsprojekter.

Vi arbejder primært med teknologierne Proficy iFix, Proficy Historian, PAS -X, Siemens S7 PLC og Siemens WinCC Flexible. Alle automationssystemer er tilsluttet vores fælles procesnetværk. iFix programmering vil også være en del af dit job, specielt i forbindelse med optimering og forbedring af vores SCADA systemer.

Du vil medvirke til at sikre, at vi opererer og validerer vores automatikudstyr, i overensstemmelse med eksterne myndigheders og interne Novo Nordisks krav. Du vil ligeledes støtte dine teamkollegaer i denne proces.

Kvalifikationer
Først og fremmest er du en team-player, og du brænder for at udvikle dit speciale og lære nye ting. Du har et godt humør og en struktureret tilgang til at løse udfordringer på en systematisk, enkel og effektiv måde.

Du har gode kommunikationsevner, både skriftligt og mundtligt, og du kan kommunikere teknisk komplekse informationer til ikke-tekniske kolleger.

Du har sikkert en ingeniør eller lignende akademisk baggrund, med mindst 3 til 5 års erfaring. Det er et krav at du har erfaring med iFix og Historian, samt Computer-System-Validation i et GMP reguleret miljø.Har du derudover erfaring med GAMP og 21 CFR Part 11, er det en yderligere fordel.

Du er en engageret, struktureret, kvalitetsbevidst person, der tager ansvar for både din egen og afdelingens opgaver. Du trives i et arbejdsmiljø hvor ændringer kan ske hurtigt, og du formår at holde fokus eller ændre kurs alt efter hvad der kræves. Du stortrives i en rolle, hvor du kan udfolde din faglige viden og bringe din argumenter og forhandlingsevner i spil. Du byder forandringer velkommen og udfordrer gerne vores måde at gøre tingene på, så vi bliver endnu bedre.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Hvis du ønsker at vide mere om stillingen, så kontakt Anders Engberg på + 45 3079 2628.

Ansøgningsfrist
30. maj 2014

Danmark - Kalundborg Produktion
11-Apr-2014 Kemiker Lab
Har du lyst til at arbejde i et team i vækst med inspirerende kolleger med team spirit? Sætter du din faglighed højt og er omhyggelig med det, du laver? Har du sans for sproglig formulering og synes du også det...

Kemiker Lab

  • Produktion
  • Danmark - Kalundborg

Har du lyst til at arbejde i et team i vækst med inspirerende kolleger med team spirit? Sætter du din faglighed højt og er omhyggelig med det, du laver? Har du sans for sproglig formulering og synes du også det er sjovt at være med i praktisk arbejde i laboratoriet? Så kunne du være præcis den kollega, vi søger i Seed Lab and IPC?

Om afdelingen
Biopharmaceuticals er en del af Novo Nordisks produktion, hvor vi producerer en række af Novo Nordisks produkter. Vi er i alt 1.800 medarbejdere fordelt på flere af Novo Nordisks sites på Sjælland. Du bliver en del af Biopharmaceuticals produktion i Kalundborg, hvor vi producerer den aktive ingrediens i produktet NovoSeven® (hæmofili-præparat). Produktionsprocessen består af mammal celledyrkning med efterfølgende kromatografisk oprensning og vi producerer døgnet rundt, året rundt. Vi udgør i alt ca. 100 medarbejdere på det 3.500 mand store site i Kalundborg.

Jobbet
Seed Lab and IPC er et team på 4 kemikere og 9 laboranter. Vi udfører den første del af opformeringsprocessen i produktionen af NovoSeven®. Vi udfører analyser som overvågning af produktionsprocessen. Vi indgår således i produktionslinjen og er samtidigt et laboratorium. Dette giver en spændende bredde i opgaver og dagligdag. Vi følger skarpt op på driften hver dag, håndterer hændelser, reviewer logbøger og opdaterer SOP’er. Dokumentation og overholdelse af krav og regler er en vigtig brik i arbejdet, som sker i tæt samarbejde med vores QA afdeling. Du vil arbejde tæt sammen med laboranter og øvrige kemikere i teamet, såvel i laboratoriet som ved skrivebordet.

Produktionsdelen udgøres af vores Podelaboratorium, hvor vi under aseptiske forhold opformerer mammale celler fra ampul til produktionstank. Laboratoriedelen omfatter IPC (In Process Control) analyser, pH, celletælling, mikroskopi, glucose, titreringer, ELISA og PCR under kvalificering. I jobbet indgår kvalificering af udstyr og analysemetoder. Vi står overfor at skulle kvalificere både nye nitrogenfrysere og inkubatorer, samt nyt udstyr til ELISA og at skulle indføre PCR og indrette et nyt laboratorium.

Kvalifikationer
Du har en akademisk naturvidenskabelig uddannelse, ingeniør, cand. polyt, cand. scient eller cand. pharm. Du taler og skriver dansk og engelsk på højt niveau. Din erfaring og dit kompetenceniveau afgør omfanget af opgaver og ansvar, hvilket gør det til et udfordrende job, hvad enten du er nyuddannet eller har erfaring. Du kan kombinere højt kvalitetsniveau med overholdelse af deadlines, er omhyggelig og gør dig umage med dit arbejde. Du er fleksibel og tør være åben og ærlig, da det er nøglen til tillid og samarbejde i et team. Du skal kunne fokusere, samtidig med at du har overblik over dine opgaver og deadlines.

Din positive indstilling og dit smittende engagement gør det nemt for dig at samarbejde med kolleger uanset organisatorisk placering.

Novo Nordisk i Kalundborg er en by i byen. Vi er 3.500 mennesker i alt fordelt på 16 fabrikker med en lang række forskellige funktioner, så der er rige muligheder for faglig udvikling.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Trine Wolff på + 45 3075 5032.

Ansøgningsfrist
27. april 2014

Danmark - Kalundborg Produktion
11-Apr-2014 Automatikingeniør
CMC API Development har ca. 350 ansatte. Vi er ansvarlige for API fremstilling og proces-udvikling af nye API kandidater til alle Novo Nordisk udviklingsprodukter. Dette inkluderer områderne gæring, dyrkning, k...

Automatikingeniør

  • Forskning og Udvikling
  • Danmark - Bagsværd

CMC API Development har ca. 350 ansatte. Vi er ansvarlige for API fremstilling og proces-udvikling af nye API kandidater til alle Novo Nordisk udviklingsprodukter. Dette inkluderer områderne gæring, dyrkning, kemisk syntese, grovrens og finrens. Der er stor fokus på en stabil produktion og altid et stort antal spændende projekter i pipelinen. Vi søger derfor en dygtig automatikingeniør, som har lyst til at beskæftige sig med drift og kvalificering af proceskontrolsystemer samt deltagelse på større og mindre investerings-projekter.

Om afdelingen
Vi er en teknisk supportafdeling og vores primære opgaver er at supportere og sikre en stabil drift. Vi er ca. 45 personer og dækker over mange faggrupper herunder: projektledelse, automatik, vedligehold, kalibrering, SAP og drift af forsyningsanlæg. I teamet Technical Compliance and Automation løser vi en lang række opgaver i forbindelse med drift og vedligehold af automatik-systemer samt projektkoordinering af mindre anlægsopgaver.

Jobbet
Du bliver en del af et team på 9 engagerede ildsjæle, som er dedikerede til at supportere vores kunder på tværs af alle pilotanlæg i Bagsværd. Din opgave er overordnet support på automatik, hvor vi har SattLine og DeltaV som PCS systemer. Jobbet indebærer sikring af at styresystemerne er i compliance med gældende regler, håndtering af daglig support samt trouble shooting i kontrolrummet. Du vil gennemføre ændrings- og kvalificeringsopgaver i samarbejde med vores kunder i piloterne.

Som person er du god til at holde styr på dine opgaver og du arbejder selvstændigt. Du er selvsikker og er i stand til at sætte dig igennem og få indflydelse. Dine stærke kommunikative kompetencer gør dig til en troværdig og overbevisende kommunikator.

Du formår at sprede entusiasme og energi omkring dig, og du besidder stærke networking og relationelle kompetencer.

Vi er en organisation som løbende har behov for at udvikle nye ledere, derfor vil ambitioner om ledelse være at en fordel.

Du kommer helt sikkert ikke til at kede dig og kan se frem til en afvekslende hverdag i samarbejdet med vores kunder på tværs af organisationen samt med vores eksterne leverandører.

Kvalifikationer
Du har gennemført en akademisk uddannelse og har erfaring samt en stærk interesse for automatik. Vi er underlagt store kvalitetskrav, så forståelse og kendskab til GMP, GAMP, ISA95/88 er et plus. Høj disciplin omkring opgaveudførelse og grundig dokumentation af alt udført arbejde er et krav. Vi lægger vægt på, at du har et godt humør og kan lide at tage fat i opgaverne, også når de ikke bliver lagt tilrette foran dig.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med mange gode kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Andreas Heuer på + 45 3079 8595.

Ansøgningsfrist
30. april 2014

Danmark - Bagsværd Forskning og Udvikling
11-Apr-2014 Processupporter til Victoza
Novo Nordisk skaber fortsat stor vækst og gode resultater. Derfor har vi brug for en processupporter med højt energiniveau og lederambitioner til vores Purification Plant i Kalundborg. Med udgangspunkt i din vi...

Processupporter til Victoza

  • Produktion
  • Danmark - Kalundborg

Novo Nordisk skaber fortsat stor vækst og gode resultater. Derfor har vi brug for en processupporter med højt energiniveau og lederambitioner til vores Purification Plant i Kalundborg. Med udgangspunkt i din videregående uddannelse, din viden om kemi og din sans for kvalitet, får du en vigtig rolle i vores arbejde med at understøtte produktionen.

Din nye arbejdsplads er Novo Nordisks produktions-site i Kalundborg. Vi er 2.600 kolleger, der bl.a. producerer 50 % af verdens insulin. Du kan glæde dig til at blive del af en organisation, der altid stræber højere. Alle medarbejdere har naturligvis personlige udviklingsplaner, og vi har sat vores videndeling i system i formaliserede faglige netværk.

Om afdelingen
Dit nye arbejde handler om finrensning af det nye og spændende produkt Victoza i afdelingen PPIII. Du bliver en del af et team på 18 akademikere og teknikere. Vi har ansvaret for processer og udstyr. Det drejer sig bl.a. om kromatografiske søjler, fældning, centrifugering, organisk syntese og råvare/solvent blanderi.

Jobbet
I dette job vil du primært skulle arbejde med vores råvare solvent afsnit, som er et område under stor udvikling, og du vil derfor få mulighed for at forme og sætte retning for denne slags processer fremadrettet. Du supporterer operatørerne i driften og træffer hurtigt beslutninger, hvis der opstår uforudsete driftsstop eller afvigelser – og efterfølgende identificerer du årsagen, ved at bruge systematisk problemløsning og lean-værktøjer. Daglig rapportering og dokumentation er derfor også meget vigtige ingredienser i dit nye job. Herunder håndterer du store datamængder, som du forvandler til forståelige procesbeskrivelser, der viser sammenhænge mellem data og processer.

Kvalifikationer
Kemisk viden og forståelse af processer og udstyr. Du har en videregående kemisk orienteret uddannelse (fx kemi ingeniør), som gør, at du er god til kemi og forstår sammenhængen mellem processer og udstyr. Der er GMP i alt, hvad vi laver, så forståelse og kendskab til dette er et stort plus. Samtidig er du skarp på rapportering og dokumentation, og i den sammenhæng er det vigtigt du kan lide at behandle og se på data. Derudover er det vigtigt, at du trives i en hverdag med højt tempo, hvor du har rigtigt mange kontakter på alle niveauer og på tværs af faggrupper. Da tæt samarbejde er en grundlæggende forudsætning for vores succes, skal du også være udpræget team-player. Vi har en forventning om du bor inden for en rimelig afstand af Kalundborg eller være villig til at flytte.

Gør dig synlig til et fremtidigt job i produktionen: Vi har løbende nye stillinger inden for processupport. Så er der ikke en stilling, der rammer plet lige nu, så giv din interesse til kende ved at lave en uopfordret ansøgning via novonordisk.com/UA.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så er du meget velkommen til at kontakte Kim Ejlersen på + 45 3075 1099.

Ansøgningsfrist
25. april 2014

Danmark - Kalundborg Produktion
11-Apr-2014 Laborant til Protein Test Maskinen
Vi søger fagligt stærke laboranter som trives med at arbejde med mange forskellige teknologier inden for rekombinant protein produktion til en afdeling under Protein Chemistry området. Om afdelingen...

Laborant til Protein Test Maskinen

  • Forskning og Udvikling
  • Danmark - Måløv

Vi søger fagligt stærke laboranter som trives med at arbejde med mange forskellige teknologier inden for rekombinant protein produktion til en afdeling under Protein Chemistry området.

Om afdelingen
Protein Chemistry området består af 20 forskningskemikere og 25 laboranter fordelt på tre forskellige forskningsenheder. Protein Chemistry er en del af Diabetes Protein Engineering funktionen i Diabetes Research Unit (DRU) og er involveret i den tidlige fase af frembringelsen af nye terapeutiske proteinkandidater til behandling af diabetes og fedme. Vore medarbejdere arbejder primært inden for vores ekspertiseområder som er proteinoprensning, analyseudvikling og karakterisering.

Protein Test Maskinen er en afdeling på 15 personer, som udgør en yderst vigtig basis for at supportere den tidlige R&D pipeline for Novo Nordisk. Formålet er løbende at kunne levere et højt antal færdigoprensede rekombinante proteiner til de første analyser af proteinernes biologiske og terapeutiske potentiale. Leveringen af proteiner foregår på basis af en high-throughput teknologisk platform som er det centrale omdrejningspunkt for afdelingen. Proteinerne vil blive delvist karakteriseret for at sikre høj kvalitet.

En stor ekspertise indenfor rekombinant ekspression og proteinoprensning er nødvendig for at kunne levere proteinerne og afdelingen benytter sig af adskillige teknologier inden for både protein kemi og molekylær biologi. Protein Test Maskinen har en meget stor berøringsflade med hele forskningsorganisationen, da den samarbejder med flere forskningsprojekter og grupper både i Novo Nordisk DK og Novo Nordisk Beijing.

Jobbet
Du vil primært komme til at arbejde med protein oprensning teknikker. Du vil arbejde med etablering og kørsler af nye oprensningsscreeninger og oprensningsprocedurer ved brug af state-of-the-art oprensnings teknologi. Endvidere omfatter arbejdet UPLC/HPLC kørsler, anvendelse af eletroforetiske metoder, MS analyse og stabilitets studier af de oprensede proteiner. Erfaring inden for ekspression af proteiner i mammale cellelinjer eller mikrobielle organismer betragtes som en fordel. Du forventes at bidrage til løbende optimering af disse discipliner og på baggrund af din store praktiske erfaring deltage aktivt i den videre udvikling af afdelingen.

Kvalifikationer
Du har en solid baggrund og ekspertise indenfor proteinoprensning og anvendelse af FPLC systemer (ÄKTA) samt proteinhåndtering og analyse. Du har ligeledes kendskab til metoder indenfor rekombinant protein ekspression. Du trives godt med at levere til deadlines, er omstillingsparat i forhold til dit job, tager gerne imod nye teknologiske udfordringer og arbejder selvstændigt. Du har ordenssans og er vant til løbende at optimere dine arbejdsgange, så de bliver endnu bedre. PC kendskab er en fordel og god praksis for data dokumentation er påkrævet. Som person er du positiv, fleksibel og har et godt humør.

Du er udadvendt og er god til at arbejde sammen med dine kollegaer.

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel

Kontakt
Vil du vide mere om stillingen, så kontakt Allan Shaw på + 45 3079 4403.

Ansøgningsfrist
30. april 2014.

Danmark - Måløv Forskning og Udvikling
10-Apr-2014 Teknisk processupporter til Pakkeri
Vil du arbejde med verdensklasse produktion af Novo Nordisks montage og pakning af insulinprodukter i Kalundborg. Og er du klar til et markant ansvar med fokus på kvalitet, produktion og processer samt faglig o...

Teknisk processupporter til Pakkeri

  • Produktion
  • Danmark - Kalundborg

Vil du arbejde med verdensklasse produktion af Novo Nordisks montage og pakning af insulinprodukter i Kalundborg. Og er du klar til et markant ansvar med fokus på kvalitet, produktion og processer samt faglig og personlig udvikling? Så er du sikkert vores nye kollega i processupporter teamet, der består af 15 højt engagerede medarbejdere? Vi skaber fortsat stor vækst og gode resultater og har derfor brug for en processupporter med højt energiniveau og gerne lederambitioner.

Om afdelingen
Du kommer til at indgår i Prefilled Device Support, Site Ka i Kalundborg. Vi supporterer driften af montage- og pakkelinier, optimerer processer og sikrer udstyrets valideringstilstand, så vi kan holde antallet af afvigelser på et minimum. Vi håndterer ændringer og løser problemer effektivt og i komplet overensstemmelse med gældende krav.

Jobbet
Dit ansvar er at supporter montage- og pakkelinjer i afdelingen Prefilled Device, således at kravene til validering, kvalitet, compliance og GMP er overholdt. Du vil få ansvaret for en konkret produktionslinje, hvor din hverdag byder på tekniske udfordringer og du løser pludseligt opståede problemer i produktionen, også her anvender du LEAN værktøjerne. Du sørger hele tiden for at skabe fremdrift i dine opgaver bl.a. ved at involvere relevante kolleger fra andre områder til opgave- og problemløsning. Du deltager i inspektioner - både eksterne og interne audits.

Din primære kontaktflade er operatører, reparatører og ledere i produktionen samt logistik og QA. Du sikrer din succes ved at holde fokus på dels kvalitet og leadtime på dine opgaver samt sikre en god relation til dine interessenter.

Du trives som en del af et engageret team, hvor vi lægger stor pris på samarbejde og trivsel. Derfor er det helt essentielt, at du er både åben og udadvendt og samtidig har en god portion empati. Teamet står over for en spændende udfordring, som er at skabe stabile processer, samtidig med at kapaciteten øges. Ud over det øges kravet om compliance hele tiden. Området er i det hele taget i en rivende udvikling, hvor vi har mange bolde i luften og mange interessenter at forholde os til.

Kvalifikationer
Du har en videregående uddannelse med et videnskabelig eller teknisk fokus som fx proces- eller produktionsingeniør gerne suppleret med relevant erfaring. Du er dit ansvar bevidst og formår at træffe de nødvendige beslutninger for at løse udfordringer med sans for effektivitet og kvalitet. Du har et godt overblik og en skarp analytisk sans, som gør det nemt for dig at skære ind til benet og gennemskue sammenhænge fx mellem processer, materialer og udstyr.

Er du nyuddannet skal du besidde et stort drive for at lykkes i stillingen, og du skal indstille dig på en stejl læringskurve. Du taler og skriver flydende engelsk og dansk.

I Novo Nordisk baseres beslutninger og handlinger på deres indflydelse på samfundet, miljøet og muligheden for at skabe økonomisk overskud. Det skaber tilsammen en ansvarlig kultur med et sundt og engageret arbejdsmiljø.

Kontakt
Vil du vide mere om stillingen, så kontakt Ole S. Iversen på + 45 3075 2649.

Ansøgningsfrist
5. maj 2014.

Danmark - Kalundborg Produktion
10-Apr-2014 Specialist drømmejob i QA til større projekter
Vil du være med til at præge og sætte faglig retning for en afdeling i rivende udvikling og vækst? Brænder du for at gøre en forskel og forbedre mange menneskers liv ved at sikre kvaliteten af insulinproduktion...

Specialist drømmejob i QA til større projekter

  • Kvalitetssikring
  • Danmark - Kalundborg

Vil du være med til at præge og sætte faglig retning for en afdeling i rivende udvikling og vækst? Brænder du for at gøre en forskel og forbedre mange menneskers liv ved at sikre kvaliteten af insulinproduktionen i Product Supply? Har du solid erfaring med QA og ønsker du at gå specialistvejen ved at prøve kræfter med større kvalificering- og valideringsprojekter? Så er du måske den rette person til jobbet som Senior QA Kemiker til QA for Insulin Manufacturing II i Kalundborg, verdens største insulinproduktion.

Om afdelingen
QA for Insulin Manufacturing II er en afdeling i rivende udvikling med pt. 35 engagerede og motiverede medarbejdere fordelt på 3 teams. Vi er ansvarlige for Novo Nordisks produktion af human insulin API, lige fra gæring til finrensning.

Vores fornemmeste opgave er at yde kvalitets support til alle aktiviteter i produktionen både til daglig drift og større projekter. Du vil blive en del af teamet med de mest erfarne QA medarbejdere, der er med til at drive de store strategiske projekter inden for QA.

Jobbet
Dit overordnede ansvar er at sætte retning for kvalitet og compliance ud fra de myndighedskrav, vi efterlever. Det gør du ved at udfordre og godkende forslag og løsninger samt coache produktionen til at levere i den rette kvalitet.

Som senior QA medarbejder bliver du afdelingens orakel, der har svar på alle detaljer i forbindelse med GMP. Dit job bliver f.eks. at sagsbehandle validerings- og kvalificeringsdokumentation samt løbende at vurdere compliance-niveauet og identificere og prioritere eventuelle gaps. Som den erfarne QA kemiker får du en særlig opgave i at drive og lede større projekter indenfor blandt andet kvalificering og validering.

Du vil få mange faglige udfordringer i en meget varierende hverdag, hvor ikke to dage er ens. I tilfælde af komplicerede afvigelser er det dig, der er med til at sætte retning for, hvordan de løses. Du får en stor kontaktflade til produktionens afdelinger, og det er derfor væsentligt, at dine kommunikative evner er stærke, og at du kan samarbejde på tværs i organisationen.

Kvalifikationer
Du har en akademisk uddannelse som fx cand.scient, ingeniør, pharmaceut eller dyrlæge kombineret med erfaring fra farmaceutisk produktion. Da vi søger en erfaren senior QA med en stærk faglig profil forestiller vi os, at du har mindst 5 års erfaring med fortolkning af GMP regler indenfor QA, alternativt mindst 7 års erfaring med arbejdet i GMP regulerede miljøer indenfor farmaceutisk produktion eller en viden, der svarer til dette. Med din baggrund inden for GMP ved du, hvordan komplicerede afvigelser skal løses, og hvordan vi får et godt samarbejde både i afdelingen og med vores samarbejdspartnere.

Du beskrives som en person med et godt humør og en åben tilgang til dine omgivelser. Du skal selvstændigt kunne drive processer og med en god energi kunne håndtere udfordringer, også i de mere travle perioder.

Site Kalundborg er en by i byen, kun godt en times kørsel fra København. Området er på 1.350.000 m2 med eget vejnet. Vi er 3.500 medarbejdere i alt fordelt på 16 fabrikker, og vi producerer bl.a. 50 % af verdens insulin. Site Kalundborg kan helt kort sammenfattes til: udviklingsmuligheder uden ende.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Du kan lære mere om Novo Nordisk Product Supply og arbejdet i QA ved at bruge linket www.novonordisk.com/careers/QA

Kontakt
Vil du vide mere om stillingen så kontakt Nanna-Freja Riis Larsen på + 45 3079 1736.

Ansøgningsfrist
28. april 2014

Danmark - Kalundborg Kvalitetssikring
10-Apr-2014 Kvalitetsansvarlig kemiker til nyt pilot plant i Bagsværd
Har du lyst til at tage ejerskab for at sikre kvaliteten i et helt nyt anlæg til oprensning af fremtidens insuliner og GLP-1’er i pilotskala, så er muligheden her. Vi står overfor udfordringen at skulle øge fre...

Kvalitetsansvarlig kemiker til nyt pilot plant i Bagsværd

  • Forskning og Udvikling
  • Danmark - Bagsværd

Har du lyst til at tage ejerskab for at sikre kvaliteten i et helt nyt anlæg til oprensning af fremtidens insuliner og GLP-1’er i pilotskala, så er muligheden her. Vi står overfor udfordringen at skulle øge fremstillingskapaciteten indenfor vores stigende udviklingsportefølje af diabetes produkter. Til den opgave søger vi en dygtig og engageret kemiker.

Om afdelingen
Afdelingen er Downstream Pilot Plants, som hører under området CMC API Development. Afdelingen består af 4 eksisterende pilot plants, der oprenser proteiner til toksikologiske og kliniske studier og et supportteam, der understøtter driften af anlæggene.

Jobbet
Vi tilbyder en spændende stilling som kvalitetsansvarlig kemiker. Du bliver ansvarlig for kvalitets-fagpakken i projektet, hvor du i tæt samarbejde med de øvrige medarbejdere i teamet får til opgave at gennemføre kvalificering iht. GMP-reglerne og bringe det nye pilotanlæg i stabil drift.

Dermed får du en vigtig opgave i at skabe en rød tråd igennem projektforløbet, således at de beslutninger og valg vi træffer undervejs er med til at sikre gode simple løsninger, der i sidste ende betyder stabil drift og compliance med GMP-reglerne. Når anlægget er indkørt og i drift, vil opgavernes art ændre sig til at fokusere på den løbende drift, men stadig med kvalitet og GMP som primært fokus.

Jobbet kræver, at du har tæt samarbejde med de andre i teamet samt vores samarbejdspartnere, herunder det rådgivende ingeniørfirma, QA og teknisk support.

Vi tilbyder et spændende og afvekslende job i et åbent og dynamisk arbejdsmiljø, hvor du vil opleve stor frihed til at løse opgaverne på din måde. Du vil i teamet få en flok engagerede og hjælpsomme kolleger, der ligesom du synes, at det er vigtigt, at det er sjovt at gå på arbejde.

Kvalifikationer
Du har en naturvidenskabelig uddannelse som f.eks. cand. scient. eller ingeniør. Du forventes at tage lederskab for kvalitets-fagpakken – og vores drømmekandidat har tilsvarende erfaring med kvalificering og validering ifm. et større anlægsprojekt i den farmaceutiske branche.

Det er vigtigt, at du det ene øjeblik evner at bevæge dig på konceptuelt niveau ift. de overordnede valideringsprocedurer, for øjeblikket efter at kunne finde en praktisk løsning på eks. en valideringsafvigelse. Det er påkrævet, at du tør tage initiativ til at opsøge viden og at du kan beslutte, hvordan du kommer videre med opgaverne.

Da det rådgivende ingeniørfirma er fra England, skal du være flydende på engelsk.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Thomas Busch på telefon + 45 3079 0533.

Ansøgningsfrist
7. maj 2014.

Danmark - Bagsværd Forskning og Udvikling
10-Apr-2014 Erfaren projektleder til Facility Management
Har du solid erfaring med projektledelse, og kan du sikre rettidig eksekvering af større, komplekse byggeprojekter? Så læs endelig videre. For at kunne gennemføre ændringer på vores bygninger og installatione...

Erfaren projektleder til Facility Management

  • Produktion
  • Danmark - Bagsværd

Har du solid erfaring med projektledelse, og kan du sikre rettidig eksekvering af større, komplekse byggeprojekter? Så læs endelig videre.

For at kunne gennemføre ændringer på vores bygninger og installationer lukker vi den aseptiske produktion i Bagsværd ned to gange om året. Vi har derfor brug for en erfaren projektleder til denne kritiske og tværorganisatoriske opgave.

Om afdelingen
Du bliver en del af Facility, Metrology and Fine Mechanics, hvor vi er 40 kolleger, som arbejder målrettet for at yde support til den aseptiske produktion. Vi sikrer forsyninger af bl.a. vand, damp og ventilation og overvåger at disse er stabile. Vi sikrer, at alt udstyr i produktionen er kalibrereret og at huset fremstår i god stand. Vores værksted fremstiller reservedele og udstyr til den aseptiske produktion.

Jobbet
Som projektleder skal du stå for både planlægning og eksekvering af nedlukningen af vores produktion om sommeren og vinteren. Du skal sikre, at alle arbejder i og på bygningen udføres til tiden, til den aftalte pris og i henhold til gældende retningslinjer for en aseptisk produktion dvs. i henhold til GMP.

Sommer og vinter nedlukning er for os to meget kritiske perioder, hvor vi skal nå at udføre alt det arbejde, vi ikke kan lave mens produktionen kører. Det betyder, at der arbejdes 24/7 i nedlukningsperioden, og at en afgørende succes faktor er, at deadline for genopstart af produktionen overholdes.

Foruden disse to årlige projekter vil du ligeledes blive trænet til rollen som ekspert i vores interne projektledelsessystem, ligesom du skal lede øvrige byggeprojekter. Du vil derfor blive en vigtig spiller i forbindelse med vores samlede projekt portefølje.

Kvalifikationer
Du har en videregående uddannelse, en god teknisk forståelse og sans for kvalitet. Vi lægger vægt på, at du har en dokumenteret og solid projektledererfaring, som du kan have erhvervet fra bygge- og anlægsbranchen eller en farmaceutisk virksomhed.

Nedlukningsopgaven kræver stort overblik, en evne til at gøre det komplekse simpelt og modet til at prioritere. Gode kommunikationsevner er ligeledes vigtige for at få succes i jobbet. For være en succes i dette job vil struktur, analytiske evner og leder erfaring blive set som et plus.

Endelig er det en klar forudsætning, at du er fleksibel i forhold til, hvornår du afholder ferie, da nedlukningerne foregår i sommerferien og mellem jul og nytår. Vi forventer også at du behersker både dansk og engelsk i skrift og tale.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden inden for diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Jimmie Madsen på telefon + 45 3079 5992.

Ansøgningsfrist
27. april 2014.

Danmark - Bagsværd Produktion
09-Apr-2014 Supporter fyldeafdeling
I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her ha...

Supporter fyldeafdeling

  • Produktion
  • Danmark - Kalundborg

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel. Finder du denne udfordring inspirerende og udfordrende er du er måske den nye supporter i vores tekniske support med ansvar for vores avancerede fyldelinier fra Bosch.

Om afdelingen
I Biopharm divisionen af Novo Nordisk har vi blandt andet ansvaret for at producere NovoSeven®, de kommende generationer af hæmofilipræparater, Glucagon og andre Biopharm produkter. Vi oplever en stigende efterspørgsel og har valgt at etablere en ny fabrik i Kalundborg for at sikre fyldning og pakning af vores produkter. Fyldefabrikken vil indeholde følgende processer; Vask og Sterilisation, Formulering, Fyld og Frysetørring.

Jobbet
Vores nye aseptiske fyldefabrik er udstyret med helt nye fyldelinier fra Bosch der netop nu er under kvalificering. Du skal primært supportere disse fyldelinier og det tilhørende perifere udstyr i det aseptiske område, med såvel daglige support som optimeringsopgaver. Du får mulighed for både at blive en vigtig GMP sparringspartner for drift teamets reparatører, der klarer de daglige praktiske vedligeholdelsesopgaver, og proceskemikere i deres arbejde med at sikre processer vedligeholdes og løbende optimeres.

Da du vil fungere som support for et team af kvalificerede reparatører, så vil det være en stor fordel du har have teknisk indsigt og forståelse for systemerne, så du på den ene side kan supportere og sparre med reparatørerne i dagligdagen ligesom du understøtte fabrikkens proces kemikere i deres arbejde med at sikre udstyrets validerede tilstand. Du vil få mulighed for selvstændigt at drive optimerings projekter i området, og i det hele taget være med til at sikre vores nye fyldelinier hver gang everer til tiden i verdensklasse.

Vi ser frem til at invitere dig ind i et team, der består af 21 fagligt dygtige, ambitiøse og målrettede medarbejdere og giver dig samtidig mulighed for at sætte dit præg på fremtidige arbejdsgange og de organisatoriske rammer.

Kvalifikationer
Du har formentlig en ingeniør eller maskinmester baggrund, og du har gennem din karriere opnået erfaring med drift, vedligehold og support opgaver af lignende systemer i den, gerne i den farmaceutiske industri.

Det forventes, at du anvender officepakken på et højt niveau, og du ubesværet kan tale og skrive engelsk.

Uanset din baggrund skal du have viden om GMP – gerne relateret til aseptisk produktion. Har du tilmed erfaring fra farmaceutisk produktion samt kendskab til kvalificering af udstyr, samt LEAN, er det absolut et plus.

Kvalitet og præcision er afgørende i vores industri, så det er vigtigt, at du er kvalitetsbevidst og har lyst til og har erfaring med skriftlig dokumentation der vil blive en stor del af dit arbejde Du formår proaktivt at etablere et godt arbejdsnetværk og gode relationer samt tænke optimering i enhver arbejdsopgave. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Peter René Jensen på +45 3079 2663.

Deadline
25.april 2014

Danmark - Kalundborg Produktion
08-Apr-2014 Laborantpraktikanter
Til ansættelse pr. 1 Februar 2015 Vi søger 16 laborantpraktikanter til Bagsværd, Gentofte, Hillerød, Måløv og Kalundborg. Bliv en del af et udfordrende, internationalt forskningsmiljø...

Laborantpraktikanter

  • Elev
  • Danmark - Måløv

Til ansættelse pr. 1 Februar 2015

Vi søger 16 laborantpraktikanter til Bagsværd, Gentofte, Hillerød, Måløv og Kalundborg.

Bliv en del af et udfordrende, internationalt forskningsmiljø
Vil du arbejde i en branche, der har fingeren på pulsen? Er du dynamisk har du gå-på-mod og kan du lide at arbejde systematisk? Så bliv laborantpraktikant i Novo Nordisk, som en del af et engageret team, der brænder for at skabe gode resultater. Du skal være i gang med eller have gennemført den teoretiske del af din laborantuddannelse. Har du derudover erfaring fra f.eks. fritidsjob eller udlandsophold, så kan det være en fordel.

Hvordan er uddannelsen?
Som laborantpraktikant får du bl.a kendskab til avanceret protein- eller molekylærbiologi, moderne bioteknikker som f.eks gensplejsning og godt indblik i det almene laboratorie- og driftsarbejde. Vi benytter os af det nyeste udstyr og teknikker inden for alle områder. I løbet af din 1-årige praktiktid vil din vejleder og dine kolleger sørge for, at du lærer relevante teknikker og apparatur at kende.

Du kan se frem til at blive en del af et udfordrende og internationalt forskningsmiljø, hvor du kan udvikle dig både fagligt og personligt. Samtidig har vi også plads til at have det sjovt.

Arbejdssted: Dit arbejdssted kan være enten i Bagsværd, Gentofte, Hillerød, Måløv, Kalundborg.

Ansøgning:
Skriv i din ansøgning, hvilke arbejdsområder, teknikker, medicinske forsøg mv. du gerne vil arbejde med.

Vedhæft dine eksamenspapirer og cv med oplysning om personlige data, dine interesser og evt. erhvervserfaring.

Kontakt
Har du spørgsmål, kan du kontakte Isabell Andresen på tlf. 3079 7327.

Ansøgningsfrist
5 Maj 2014

Danmark - Måløv Elev
08-Apr-2014 Tekniker til HVAC Team
I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her ha...

Tekniker til HVAC Team

  • Produktion
  • Danmark - Kalundborg

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel. Finder du denne udfordring inspirerende og udfordrende er du er måske den nye håndværker i vores tekniske support der har ansvaret for vores avancerede ventilation, HVAC.

Om afdelingen
I Biopharm divisionen af Novo Nordisk har vi blandt andet ansvaret for at producere NovoSeven®, de kommende generationer af hæmofilipræparater, Glucagon og andre Biopharm produkter. Vi oplever en stigende efterspørgsel og har valgt at etablere en ny fabrik i Kalundborg for at sikre fyldning og pakning af vores produkter. Fyldefabrikken vil indeholde følgende processer; Vask og Sterilisation, Formulering, Fyld og Frysetørring.

Jobbet
Til vores drift teknikker team skal vi bruge en kollega der primært bliver tilknyttet driftopgaver i vores HVAC, ventilation, hvor du bliver fast tilknyttet drift teamet. Her deltager du derfor også dagligt i vedligehold og drift af vores øvrige forsyningsanlæg når opgaverne i HVAC tillader det.

Du bliver her den der passer de rutiner og procedurer der vedligeholder og sikrer vores HVAC holdes i perfekt stand og sikrer de til alle tider er velfungerende. Du får derudover mulighed for at etablere runderings procedurer, vedligeholdelses planer og medvirke som teknisk sparringspartner når opgaver indbefatter indgreb i ventilations anlæggende sammen med vore supportere og kemikere.

Vi ser frem til at invitere dig ind i et team, der består af 21 fagligt dygtige, ambitiøse og målrettede medarbejdere og giver dig samtidig mulighed for at sætte dit præg på fremtidige arbejdsgange og de organisatoriske rammer.

Stillingens kategori er lønklasse F3.

Kvalifikationer
Du har en teknisk håndværksmæssig baggrund, og du har gennem din karriere påvist erfaring med drift, vedligehold og support opgaver af lignende opgaver.

Det forventes, at du anvender officepakken, og et kendskab til SAP PM, MM vil være en stor fordel. Du skal kunne tale og have et godt kendskab til engelsk.

Kvalitet og præcision er helt afgørende i vores industri, så det er vigtigt, at du er kvalitetsbevidst og har lyst til og har erfaring med skriftlig dokumentation der vil blive en stor del af dit arbejde Du formår proaktivt at etablere et godt arbejdsnetværk og gode relationer samt tænke optimering i enhver arbejdsopgave. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Peter René Jensen på + 45 3079 2663.

Ansøgningsfrist
27. april 2014

Danmark - Kalundborg Produktion
08-Apr-2014 Tekniker til drift team
I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her ha...

Tekniker til drift team

  • Produktion
  • Danmark - Kalundborg

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel.

Om afdelingen
I Biopharm divisionen af Novo Nordisk har vi blandt andet ansvaret for at producere NovoSeven®, de kommende generationer af hæmofilipræparater, Glucagon og andre Biopharm produkter. Vi oplever en stigende efterspørgsel og har valgt at etablere en ny fabrik i Kalundborg for at sikre fyldning og pakning af vores produkter. Fyldefabrikken vil indeholde følgende processer; Vask og Sterilisation, Formulering, Fyld og Frysetørring.

Jobbet
Til vores drift teknikker team skal vi bruge en kollega der bliver den daglige kontaktperson for opgaver der vedrører vores nye bygning. Du bliver fast tilknyttet drift teamet og deltager derfor også dagligt i vedligehold og drift af vores forsyningsanlæg og har derudover som en del af de daglige opgaver bygningen som eget ansvarsområde.

Du bliver her den der sikrer der opbygges rutiner og procedurer der vedligeholder og sikrer vores bygning holdes i perfekt stand og til alle tider er velfungerende. Du får mulighed for at etablere runderings procedurer, vedligeholdelses planer og medvirke som teknisk sparringspartner når opgaver indbefatter indgreb i bygningen. Du vil have mulighed for at drive mindre optimerings projekter der skal sikre vores bygningsmæssige udstyr hele tiden er optimalt.

Du vil både have kontakt til vores eksterne leverandører af f.eks. elevatorer og automatiske døre og sikre de sæsonmæssige aftaler oprettes og holdes i orden, ligesom du selv vil udføre mindre opgaver der berører bygningen.

Vi ser frem til at invitere dig ind i et team, der består af 21 fagligt dygtige, ambitiøse og målrettede medarbejdere og giver dig samtidig mulighed for at sætte dit præg på fremtidige arbejdsgange og de organisatoriske rammer.

Stillingens lønkategori er F3.

Kvalifikationer
Du har en håndværksmæssig baggrund, og du har gennem din karriere påvist erfaring med drift, vedligehold og support opgaver af lignende opgaver.

Det forventes, at du anvender officepakken, og et kendskab til SAP PM, MM vil være en stor fordel. Du skal kunne tale og skrive engelsk.

Uanset din baggrund skal du gerne have viden om GMP – gerne relateret til aseptisk produktion.

Kvalitet og præcision er helt afgørende i vores industri, så det er vigtigt, at du er kvalitetsbevidst og har lyst til og har erfaring med skriftlig dokumentation der vil blive en stor del af dit arbejde Du formår proaktivt at etablere et godt arbejdsnetværk og gode relationer samt tænke optimering i enhver arbejdsopgave. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Peter René Jensen på +45 3079 2663

Ansøgningsfrist
25. april 2014

Danmark - Kalundborg Produktion
08-Apr-2014 Studentermedhjælper
Studentermedhjælpere til Steno Center for Sundhedsfremme, Steno Diabetes Center Vil du være med til at forbedre og udvikle nye tilgange indenfor patientuddannelse og patientstøtte i et dynamisk forskningsmiljø...

Studentermedhjælper

  • Studerende
  • Danmark - Gentofte

Studentermedhjælpere til Steno Center for Sundhedsfremme, Steno Diabetes Center

Vil du være med til at forbedre og udvikle nye tilgange indenfor patientuddannelse og patientstøtte i et dynamisk forskningsmiljø? I forskningsgruppen for Patientuddannelse på Steno Center for Sundhedsfremme, Steno Diabetes Center, har vi brug for to studentermedhjælpere. Vi er en fagligt bredt sammensat forskningsgruppe, der arbejder med tre områder:

- Innovative forskningsbaserede tilgange til patientuddannelse

- Psykosociale aspekter af livet med diabetes

- Diabetes og arbejdslivet

Steno Center for Sundhedsfremme er et humanistisk forskningscenter, der overordnet arbejder for at fremme livskvaliteten blandt personer med diabetes og deres familie.

Vi arbejder med både kvalitative og kvantitative metoder, med interventions- og aktionsforskning, og med inddragelse af målgrupperne for forskningen, fx personer med diabetes og sundhedsprofessionelle. Vi arbejder med sociale og psykologiske perspektiver såvel som sundhedspædagogik, og vi har en række spændende samarbejdsrelationer i nationale og internationale forskningsmiljøer.

Din profil

• Du studerer et relevant fag, fx folkesundhedsvidenskab, sundhedsfremme, pædagogik, sociologi, antropologi, kommunikation, psykologi eller lignende.

• Du mestrer dansk og engelsk i tale og skrift.

• Du er dygtig, fleksibel, engageret og har god situationsfornemmelse.

• Du har faglig og menneskelig modenhed og kan både arbejde selvstændigt og i tæt samarbejde i en tværfaglig gruppe, hvor en positiv indstilling og humoristisk sans er afgørende.

• Du er tolerant og kan kommunikere med personer med forskellig baggrund.

Det er en fordel, hvis du har kendskab til eller erfaring med forskningsprojekter, kvalitativ og kvantitative metoder, kan skrive videnskabelige tekster, har arbejdet arbejde i tværfaglige miljøer eller arbejdet med patienter og sundhedsprofessionelle. Timeantal (fleksibelt) efter aftale.

Din ansøgning skal indeholde en kort motivation og baggrund for at søge stillingen (max 1 side), et billede, CV og relevante eksamensbeviser. Ansøgningsfrist er 24. april 2014. Stillingen ønskes besat snarest.

Kontakt

Yderligere information fås hos forsker Nana Folmann Hempler nfhr@steno.dk, tlf 4443 5268 eller forskningsleder Ingrid Willaing på iwtp@steno.dk eller telefon 3075 5268.

Om Steno Diabetes Center A/S

Steno Diabetes Center er en af verdens førende institutioner inden for diabetesbehandling og forebyggelse. Steno ejes af Novo Nordisk A/S og er en 'not for profit' virksomhed, der arbejder i partnerskab med det danske sundhedssystem. Steno står for behandlingen af ca. 5.600 mennesker med diabetes.

Danmark - Gentofte Studerende
08-Apr-2014 Forsker/seniorforsker
To forskere/seniorforskere søges til forskning inden for patientuddannelse og støtte til personer med diabetes SHPC, SDC, Patient Education Research søger to forskere, der skal arbejde med at udvikle innovati...

Forsker/seniorforsker

  • Forskning og Udvikling
  • Danmark - Gentofte

To forskere/seniorforskere søges til forskning inden for patientuddannelse og støtte til personer med diabetes

SHPC, SDC, Patient Education Research søger to forskere, der skal arbejde med at udvikle innovative tilgange til effektiv patientuddannelse og psykosocial støtte til personer med diabetes. Opgaverne bliver blandt andet at være nytænkende med metoder og rammer for patientuddannelse og –støtte, herunder udvikling af forskningsbaserede koncepter samt evaluering af disse.

Vi arbejder med både kvalitative og kvantitative metoder, med interventions- og aktionsforskning, og vi arbejder med inddragelse af målgrupperne for forskningen, fx personer med diabetes, deres familier og sundhedsprofessionelle i alle dele af forskningsprocessen. Vi arbejder med sociale og psykologiske perspektiver såvel som sundhedspædagogiske perspektiver. Vi har en række spændende samarbejdsrelationer i nationale og internationale forskningsmiljøer og forventer fortsat at udvikle disse og nye relationer.

Forskerne i gruppen har en række forskellige uddannelser, fx folkesundhedsvidenskab, sociologi, antropologi, sundhedsvidenskab, psykologi og pædagogik.

Din profil

• Du har en ph.d.-grad inden for en relevant disciplin – f.eks. folkesundhedsvidenskab, sociologi, antropologi eller pædagogik og gerne efterfølgende erfaring med forskning, gerne som seniorforsker

• Du har publiceret i internationale tidsskrifter og holdt indlæg på internationale videnskabelige konferencer

• Du har erfaring med teorier og metoder af relevans for forskningsområdet (fx om social læring, socialpsykologisk teori, innovation, design thinking, aktionsforskning, evalueringsforskning, STS, epidemiologi, statistik o.lign.)

• Du har solide metodiske kompetencer inden for dit felt

• Du mestrer til fulde dansk og engelsk i tale og skrift

• Du er ambitiøs, motiveret, selvstændig, kreativ, engageret, resultatorienteret og en god kollega

• Du har faglig og menneskelig modenhed og kan arbejde både selvstændigt og som projektleder i et tæt samarbejde med en tværfaglig gruppe

Ansøgning

Vi søger to forskere til fastansættelse. Ansættelsen er i Patient Education Research, Steno Health Promotion Center, Steno Diabetes Center.

Din motiverede ansøgning, på dansk eller engelsk, skal indeholde:

• Kort motivation og baggrund for at søge stillingen (max 1 side).

• CV.

• Publikationsliste.

• Et pasfoto.

• Dokumentation for kvalifikationer og uddannelser.

• Et eksempel på en artikel, du har skrevet.

Ansøgningsfrist er den 30. april 2014. Stillingerne ønskes besat omkring 1. juli 2014. Ansættelsesvilkår er i henhold til den regionale Overenskomst 2013 (OK-13).

Kontakt

Yderligere information fås hos forskningsleder, Ingrid Willaing, iwtp@steno.dk telefon: 3075 5268.

Om Steno Diabetes Center A/S

Steno Diabetes Center er en af verdens førende institutioner inden for diabetesbehandling og forebyggelse. Steno ejes af Novo Nordisk A/S og er en 'not for profit' virksomhed, der arbejder i partnerskab med det danske sundhedssystem. Steno står for behandlingen af ca. 5.600 mennesker med diabetes.

Danmark - Gentofte Forskning og Udvikling
07-Apr-2014 Laborant/tekniker
Drømmer du om, at du med dit arbejde gør en forskel for andre mennesker, så er muligheden her. Vi er en del af Novo Nordisk A/S’s hæmofiliportefølje, og dagligt producerer vi det aktive stof i medicin til bløde...

Laborant/tekniker

  • Produktion
  • Danmark - Hillerød

Drømmer du om, at du med dit arbejde gør en forskel for andre mennesker, så er muligheden her. Vi er en del af Novo Nordisk A/S’s hæmofiliportefølje, og dagligt producerer vi det aktive stof i medicin til bløderpatienter med faktor 8-mangel, hvorved vi forbedrer mange menneskers liv.

Vi søger en laborant, bioanalytiker eller lignende, der har lyst til alsidigt arbejde i en afdeling i rivende udvikling.

Om afdelingen
Biopharm API Mammalian Cell Production i Hillerød foretager storskalaproduktion af det aktive stof (API) til faktor 8- blødermedicin. Fremstillingen sker ved dyrkning af mammale celler, som efterfølges af en proces med flere forskellige typer kromatografisk oprensning. Afdelingen er organiseret i teams, hvor dagligdagen byder på tæt samarbejde på tværs af både teams og faggrupper.

Jobbet
Du vil blive en del af laboratoriegruppen i laboratorie- og miljøteamet (lab-miljø), som bemander fabrikkens egne driftslaboratorier. Pt. består teamet af 1 teamleder, 3 kemikere, 9 laboranter/teknikere og 3 operatører.

Gruppens kernekompetence er opformering af mammale celler til produktionen, hvilket foregår i et dedikeret podelaboratorie under aseptiske forhold, hvor omhyggelighed og akkuratesse er essentielt. Herudover varetager gruppen en mængde forskellige driftsrelaterede opgaver, f.eks. fremstilling af buffere og medier mm., håndtering af de daglige driftsanalyser (celletælling, pH og metabolitter) og modtagelse, udportionering og forsendelse af prøver fra produktionen (bl.a. slutprøver fra dyrkning og rens til steriltest, virustest mm.). Som en naturlig del af alt arbejde registreres om nødvendigt hændelser og afvigelser, ligesom der følges op på disse og instruktioner opdateres løbende. Ydermere ligger der en opgave i udtagning og håndtering af miljømonitoreringsprøver, både i podelaboratoriet og i de øvrige produktionsområder.

Andre opgaver er bl.a. håndtering og vedligehold af udstyr hørende til laboratoriet (udstyrsansvarlig), udarbejdelse af ændringsager, kvalificering og validering af udstyr og metoder, optimering og problemløsningsopgaver, Lean-projekter og opfølgning på og håndtering af analysesvar fra eksterne laboratorier.

Vi er underlagt GMP-reglerne, hvorfor det er vigtigt, at du er ansvars- og kvalitetsbevidst samt fungerer godt med, at alle arbejdsgange skal dokumenteres. Du kommer til at indgå i det løbende arbejde med at optimere rutiner og arbejdsgange, hvorfor der stilles høje krav til gode samarbejdsevner, initiativ og fleksibilitet.

Arbejdet forgår i et travlt, men socialt afslappet og uformelt miljø, hvor vi lægger vægt på optimisme, vilje, humor, engagement og overholdelse af aftaler.

Kvalifikationer
Vi forestiller os at du har en faglig uddannelse som laborant, bioanalytiker eller lignende. Det vil være et stort plus med relevant erfaring, men du kan også komme i betragtning som nyuddannet. Du skal have stor lyst, og meget gerne erfaring med at arbejde med dyrkning af mammale celler, ligesom erfaring med aspetisk arbejde, meget gerne fra renrum, vil blive vægtet højt. Erfaring med GMP/ISO fra lægemiddel- eller levnedsmiddelproduktion vil tilmed være et plus. Du skal have god evne til at udtrykke dig både skriftligt og mundtligt og du skal beherske brug af Microsoft Officepakken. Du skal være struktureret, omhyggelig og engageret i dit arbejde og besidde masser af godt humør. Når det ”brænder på” skal du kunne bevare overblikket og du skal trives med at arbejde med mange bolde i luften.

Laboratoriet er bemandet alle dage hele året, hvorfor du skal være indstillet på at indgå i en vagtordning, hvor man på skift arbejder på weekend- og helligdage. Aftenvagter kan forekomme, men det sker pt. meget sjældent.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Cathrine Tamstorf på +45 3075 3563.

Ansøgningsfrist
5. maj 2014

Danmark - Hillerød Produktion
07-Apr-2014 Laborant - Research Protein Purification
Research Protein Purification afdelingen i Måløv søger en laborant til oprensning af proteiner. Om afdelingen...

Laborant - Research Protein Purification

  • Forskning og Udvikling
  • Danmark - Måløv

Research Protein Purification afdelingen i Måløv søger en laborant til oprensning af proteiner.

Om afdelingen
Vores afdeling er en del af Biotechnology funktionsområdet, som hører under forskningsområdet Biopharmaceutical Research Unit. Vi er ansvarlige for oprensning af nye proteiner til biokemisk og biologisk karakterisering. Derved er vi involveret i design og fremstilling af mange af fremtidens lægemidler.

Jobbet
Du vil komme til at arbejde med protein oprensning i varierende skala hvor Äkta Xpress eller Explorer bruges. Der kan en gang imellem være brug for oprensning i større skala med en Äkta Pilot. En stor del af dit arbejde vil bestå i at oprense mange varianter af samme protein v.h.a. high-throughput metoder. Du skal planlægge og udføre in-process analyser for at monitorere oprensningsprocesserne og sikre høj protein kvalitet. Her bruger vi primært SDS-PAGE, LC-MS og HPLC systemer som analyse værktøj. Vedligeholdelse af apparater og deltagelse i de daglige laboratorie-rutiner bliver en vigtig del af dit job. Da vi er en dynamisk organisation med mange forskningsprojekter, skal du være indstillet på løbende omstilling, have flere bolde i luften af gangen og kunne trives i en travl hverdag.

Kvalifikationer
Du er uddannet laborant, laboratorietekniker eller tilsvarende og har praktisk erfaring med proteinoprensning og analyser, inklusiv brug af Äkta systemer. Du har basal viden om proteinkemi og separationsteknikker - herunder solid viden om kromatografiske principper. Vi dokumenterer alt vores arbejde på engelsk, og forventer at du er i stand til at kommunikere med engelsktalende kolleger. Du skal kunne lide at arbejde tæt sammen med dine kolleger, da teamwork er et vigtigt element i denne stilling. Samtidig er du i stand til at arbejde selvstændigt og omhyggeligt, og du er ikke bange for at tage ansvar. Vi lægger stor vægt på et positivt mindset, fleksibilitet og godt humør.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanlig talentfulde kolleger.

Kontakt
Vil du vide mere om stillingen, så kontakt Jais Rose Bjelke på + 45 3079 4804, eller Birgitte Kjær på + 45 3079 2851

Ansøgningsfrist
26. april 2014

Danmark - Måløv Forskning og Udvikling
05-Apr-2014 Utility Supporter
I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her ha...

Utility Supporter

  • Produktion
  • Danmark - Kalundborg

I Novo Nordisk skaber vi værdi ved sætte patienterne først. Hvert tiende sekund bliver to personer diagnosticeret med diabetes, og næsten 366 millioner mennesker i hele verden har brug for os. At arbejde her handler ikke bare om at tjene til føden, men om at gøre en forskel. Finder du denne udfordring inspirerende og udfordrende er du er måske den nye Kemiker i vores tekniske support med ansvar for vores avancerede ventilation, HVAC.

Om afdelingen
I Biopharm divisionen af Novo Nordisk har vi blandt andet ansvaret for at producere NovoSeven®, de kommende generationer af hæmofilipræparater, Glucagon og andre Biopharm produkter. Vi oplever en stigende efterspørgsel og har valgt at etablere en ny fabrik i Kalundborg for at sikre fyldning og pakning af vores produkter. Fyldefabrikken vil indeholde følgende processer; Vask og Sterilisation, Formulering, Fyld og Frysetørring.

Jobbet
Vores nye aseptiske fyldefabrik er udstyret med en række utilitysystemer, der bl.a. omfatter PTW, WFI, rendamp, destillation, trykluft, HVAC, køleanlæg, varmecentral mm.

Du skal primært supportere fabrikkens clean utillity anlæg, der består af behandlet vand og damp til de sterile processer. Du bliver her en vigtig teknisk support for drift teamets reparatører, der klarer de daglige praktiske vedligeholdelsesopgaver.

Du sikrer at processerne kører som de skal og på baggrund af datarapporter fra systemerne, kontrollerer du fabrikkens tilstand opfylder de høje krav til vores medier. Du vil dagligt sammen med fabrikkens kemikere på utillity og HVAC understøtte at systemerne spiller sammen med de tilhørende produktionsanlæg og løbende sikre de vedligeholdes efter etablerede planer, og at korrigerende vedligehold udføres så hurtigt og effektivt som muligt. Du vil have mulighed for at drive optimerings projekter der skal sikre vores udstyr hele tiden er optimalt.

Du vil være teknisk support for et team af kvalificerede reparatører med ændringers sager og bistå ved problem løsning, så du skal have teknisk indsigt og forståelse for systemerne, så du på den ene side kan supportere og sparre med reparatørerne i dagligdagen ligesom du understøtte fabrikkens proces kemikere i deres arbejde med at sikre udstyrets validerede tilstand.

Vi ser frem til at invitere dig ind i et team, der består af 21 fagligt dygtige, ambitiøse og målrettede medarbejdere og giver dig samtidig mulighed for at sætte dit præg på fremtidige arbejdsgange og de organisatoriske rammer.

Kvalifikationer
Du har en håndværksmæssig baggrund, og du har gennem din karriere opnået stor erfaring med drift, vedligehold og support opgaver af lignende systemer i den farmaceutiske industri.

Det forventes, at du anvender officepakken på et højt niveau, og et kendskab til SAP PM, MM vil være en fordel. Du skal ubesværet kunne tale og skrive engelsk.

Uanset din baggrund skal du have viden om GMP – gerne relateret til aseptisk produktion. Har du tilmed erfaring fra farmaceutisk produktion samt kendskab til kvalificering af udstyr og rum, samt LEAN, er det absolut et plus.

Kvalitet og præcision er afgørende i vores industri, så det er vigtigt, at du er kvalitetsbevidst og har lyst til og har erfaring med skriftlig dokumentation der vil blive en stor del af dit arbejde Du formår proaktivt at etablere et godt arbejdsnetværk og gode relationer samt tænke optimering i enhver arbejdsopgave. Sidst, men ikke mindst, er du er udadvendt og god til at kommunikere på tværs af faggrænser – både på dansk og engelsk.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en større spiller indenfor behandling af blødninger, behandling med væksthormon og behandling med hormonterapi. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Peter René Jensen på +45 3079 2663

Ansøgningsfrist
25. april 2014

Danmark - Kalundborg Produktion
04-Apr-2014 Laborant
Vil du arbejde med Biopharms brede portefølje af produkter, og hjælpe os med at være Fast to Market? I Biopharm New Heamophilia er vi ansvarlige for support til vores produktioner i form af analyser på de nye h...

Laborant

  • Produktion
  • Danmark - Gentofte

Vil du arbejde med Biopharms brede portefølje af produkter, og hjælpe os med at være Fast to Market? I Biopharm New Heamophilia er vi ansvarlige for support til vores produktioner i form af analyser på de nye hæmofili produkter. Vi søger en laborant til vores Clot/chromogen team. Kandidater interviewes til stillingen løbende, i takt med at vi modtager ansøgningerne.

Om afdelingen
Afdelingen står for frigivelse af analyseresultater for klinikbatche (fase 3) samt stabilitetsanalyser, for vores nye hæmofili produkter.

Vi er i en spændende fase, da vi arbejder frem i mod at markedsføre vores produkter, det betyder at vi har et tæt samarbejde med vores supportlaboratorie samt produktioner for at sikre at vi lykkedes med de nye produkter.

Vi er en velfungerende afdeling med mange spændende opgaver, faglige udfordringer, mulighed for udvikling og stor kontaktflade ud af afdelingen. Her er en uhøjtidelig og god stemning med vidensdeling på tværs af teams og faggrupper. Selvom vi har mange opgaver, har vi en god balance mellem arbejde og fritid. Der er 55 medarbejdere i afdelingen, organiseret i tre analyseteams samt en stabsfunktion.

Jobbet
Clot/chromogen-teamet har ansvaret for analyse til frigivelse af klinik (fase 3) produktionen. Vi bruger følgende metoder: Clot og chromogen assay, som vi analyserer ved hjælp af biomek robot og ACL’er.

Du indgår i et team på 16 medarbejdere, fordelt på 1 teamleder, 5 kemikere og 10 laboranter.

Som vores nye medarbejder får du ansvar for at analysere vores hæmofiliprodukter, hvor du har ansvar for, at dit analysearbejde lever op til gældende GMP. I samarbejde med teamets øvrige laboranter bliver du endvidere ansvarlig for kontrol og vedligehold af udstyr. Du bliver involveret i problemløsning, indkøring og kvalificering af nyt udstyr.

Du skal samarbejde med kolleger i dit team og på tværs af afdelingen samt være i kontakt med QA, analyseudviklingsafdelinger og Biopharms QC-laboratorier.

Kvalifikationer
Du har en god analytisk baggrund og en uddannelse som laborant, laboratorietekniker, bioanalytiker eller lignende. Derudover har du erfaring med de nævnte analyseteknikker og GMP. IT vil indgå som en naturlig del af dine arbejdsopgaver. Du skal kunne dansk og engelsk i skrift og tale.

Du er god til at skabe overblik og prioritere din tid, og du har en høj grad af ansvars- og kvalitets-bevidsthed. Som person er du åben og engageret samt omhyggelig med dit arbejde, ligesom du arbejder systematisk og når dine deadlines. Du har viljen og evnen til hele tiden at forsøge at gøre tingene bedre, og forny arbejdsprocesserne og har gerne kendskab til LEAN.

Du har vist fra tidligere ansættelser, at du kan arbejde selvstændigt, og er god til at samarbejde og kommunikere med dine kolleger. Du bevarer overblikket og et godt humør i et til tider meget travlt arbejdsmiljø.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Line Rossen på + 45 3075 2313

Ansøgningsfrist
25. april 2014

Danmark - Gentofte Produktion
04-Apr-2014 Maskinmester/Ingeniør til Facility
Besidder du erfaring med drift og vedligehold af bygninger og tekniske installationer, så kan denne stilling være den helt rigtige for dig! Om afdelingen...

Maskinmester/Ingeniør til Facility

  • Produktion
  • Danmark - Hillerød

Besidder du erfaring med drift og vedligehold af bygninger og tekniske installationer, så kan denne stilling være den helt rigtige for dig!

Om afdelingen
Afdelingen Pilot Operations driver alle operationelle aktiviteter igennem hele forsyningskæden fra indkøb af materialer indtil levering af færdige produkter til vores salgsled. Vores hovedopgave er at understøtte introduktionen af nye produkter ved at modne produktionsprocesser for vores højkvalitets penne (devices).

Stillingen som bygningsansvarlig er placeret i Support teamet som sikrer kvalitet og compliance i produktionen af durable og Prefilled Devices samt eksekvering af projekter.

Jobbet
Vi søger en engageret og resultatorienteret medarbejder til et spændende job med opgaver vedrørende drift og vedligehold af vores produktionsfaciliteter i Hillerød. Stillingen kræver, at du er god til at håndtere mange opgaver samtidig, og at du trives med at have mange interessenter. De primære opgaver er at styre vores eksterne parter, som udfører service og vedligehold af bygningen, samt sikre at vores produktions faciliteter (kølefaciliteter, temperatur og fugt styrring osv.) er i compliance.

Endvidere er bygningerne ofte inspiceret af myndigheder fra hele verden, hvilket kræver, at teamet til enhver tid ajourfører afdelingens dokumentation. Ligeledes vil du indgå i et samarbejde op til inspektionerne for at sikre, at alt er på plads i forhold til overordnede krav og retningslinjer.

Kvalifikationer
Du er uddannet som maskinmester, bygningsingeniør eller lignende. Du har relevant erfaring fra disse fag, eller fra en lignende stilling. Har du viden om ISO og GMP-standarder og evnen til at sætte dig ind i disse krav, samt en god forståelse for compliance, vil dette være at foretrække.

Som person, er du kvalitetsbevidst og følger opgaverne til dørs og endvidere er det vigtigt, at du er jordnær og kan opbygge gode relationer. Du besidder lysten og erfaringen til at yde support til en meget dynamisk organisation. Du er resultatorienteret og sikrer rette kvalitet i arbejdet. Du er analytisk med stor faglig gennemslagskraft. Det er essentielt, at du er i stand til selvstændigt at prioritere de forskellige opgaver og sikre fremdrift. Derudover er du en klar kommunikator som sikrer, at dine interessenter får den rette information.

I Novo Nordisk er det dine færdigheder, dit engagement og dine ambitioner, som hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig mulighed for at arbejde med usædvanligt dygtige kolleger, og vi tilbyder dig en bred vifte af muligheder for faglig og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Thomas Bach Nielsen på + 45 3075 0052.

Ansøgningsfrist
4. maj 2014

Danmark - Hillerød Produktion
04-Apr-2014 Laborant til Immunologi
Vil du være med til at udvikle og validere ELISA metoder til lægemiddelprojekter rettet mod hæmofili, inflammation, og diabetes? Og har du lyst til at være en del af en engageret og social gruppe med et stærkt ...

Laborant til Immunologi

  • Forskning og Udvikling
  • Danmark - Måløv

Vil du være med til at udvikle og validere ELISA metoder til lægemiddelprojekter rettet mod hæmofili, inflammation, og diabetes? Og har du lyst til at være en del af en engageret og social gruppe med et stærkt fokus på faglige evner og løbende forbedringer? Så er du måske den nye kollega, vi leder efter.

Om afdelingen
Team IBA er en del af afdeling 318, CMC Bioassay, som er placeret i CMC DP Development, R&D, Novo Nordisk A/S. Teamet er fysisk placeret i Måløv og består af 6 akademikere, 12 laboranter og en teamleder.

Jobbet
Du vil efter en oplæringsperiode deltage i udvikling af ELISA og elektroforese metoder til projekter i alle kliniske forsøgsfaser. Du bliver ansvarlig for at modtage, analysere, beregne og afgive svar på analyseprøver i LIMS. Det forventes at du tager aktivt del i optimering af vores arbejdsgange i teamet, samt i udarbejdelsen af dokumenter.

Du vil udover analysearbejdet også deltage i vores daglige driftsopgaver, som bl.a. indbefatter fremstilling af reagenser, forberedelse af arbejdssedler og vedligeholdelse af apparatur. Arbejdet kræver en god ordenssans idet det foregår under GMP.

Kvalifikationer
Du er laborant eller tilsvarende og har erfaring med analysearbejde – gerne inden for ELISA og gel elektroforese - og betragter IT som en integreret del af dit arbejde. Du har kendskab til GMP og er glad for at arbejde i et team. Du er positivt indstillet overfor LEAN-tankegangen (løbende optimeringer og forbedringer). Du har udover en god humoristisk sans og godt humør, en naturlig ordenssans, er systematisk, selvstændig, motiveret og kan holde hovedet koldt i travle perioder.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Heidi Johannes på + 45 3079 6845 eller Per Jeppesen på + 45 3075 0049

Ansøgningsfrist
25. april 2014

Danmark - Måløv Forskning og Udvikling
03-Apr-2014 Metrologiingeniør – chancen for at arbejde med den nyeste teknologi
Vil du være en del af et innovativt miljø, hvor vi arbejder med den nyeste teknologi i den tunge ende af skalaen og aldrig går på kompromis med kvalitet? Er du klar til en ekspertrolle, hvor du sætter din målet...

Metrologiingeniør – chancen for at arbejde med den nyeste teknologi

  • Kvalitetssikring
  • Danmark - Hillerød

Vil du være en del af et innovativt miljø, hvor vi arbejder med den nyeste teknologi i den tunge ende af skalaen og aldrig går på kompromis med kvalitet? Er du klar til en ekspertrolle, hvor du sætter din måletekniske viden helt i front til gavn for kolleger og patienter over hele verden? Så søg jobbet som metrologiingeniør i Novo Nordisk Device Manufacturing & Sourcing i Hillerød.

Om afdelingen
Du bliver en del af Device Metrology, hvor vi tæller 28 medarbejdere, som servicerer hele device-området i Novo Nordisk. Sammen med 3 andre kolleger udgør du afdelingens Equipment Support, som står for bl.a. måleteknisk rådgivning, udvikling, implementering og vedligehold af in-process control (IPC) måleudstyr. Vi har desuden et tæt samarbejde med Device Manufacturing Development (DMD) hvor vi sammen sikrer et robust set-up, der kan udrulles i resten af verden.

Jobbet
Du får rollen som Subject Matter Expert i forbindelse med validering og kvalificering af IPC- og OPC-udstyr til produktionen. Du bliver således en central sparringspartner for DMS og DMD i alle spørgsmål vedrørende geometrisk måleteknik. Det betyder også, at du via dine høje faglighed og kvalitetsviden skal udarbejde IPC CR-sager korrekt og vejlede dine kolleger i disse, ligesom du er i dialog med eksterne samarbejdspartnere, f.eks. når vi skal udvikle nye prototyper eller indkøbe nyt udstyr.

Foruden din rådgiverrolle skal du lede en række tunge projekter bl.a. på validering af udstyr og andre tidskritiske aktiviteter. På den måde er du med til at sikre, at vi vælger de rigtige udstyrsløsninger, som kan anvendes på Novo Nordisks sites over hele verden. I alt dit arbejde har du for øje, at vi følger reglerne for en device-produktion, herunder ISO-standarder og GMP-regulativer.

Glæd dig til en udadvendt stilling, hvor du arbejder i tæt dialog med kolleger på tværs af områder, fra produktionsudvikling over produktion til QC- og QA-funktioner og med samarbejdspartnere fra ind- og udland.

Kvalifikationer
Du er uddannet maskiningeniør eller lignende, og dit cv afspejler minimum 5 års erfaring fra et lignende job, hvor du har ledet udstyrsprojekter fra specificering til implementering. Du har erfaring med brugen af metrologi i en industri med samme eller tilsvarende kvalitetskrav. Du har derfor indgående kendskab til ISO-standarder og ideelt set GMP-regler.

For at få succes i stillingen skal du kunne se dig selv i rollen som SME- og CR-ekspert. Med andre ord skal du have gode kommunikationsevner og kunne vejlede og sparre med alle fra teknikere over tekniske eksperter til projektledere og ledere.

Med dine analytiske evner kan du levere kvalitet og skabe resultater i særklasse. Du arbejder med stor selvstændighed, er velstruktureret og kendt for at tage ansvar for dine opgaver. Desuden behersker du flydende engelsk skriftligt og mundtligt.

I Novo Nordisk er det dine evner, dit engagement og dine ambitioner, der hjælper os med at forbedre mange menneskers liv. Til gengæld tilbyder vi dig muligheden for at arbejde sammen med usædvanligt talentfulde kolleger, og vi tilbyder dig en lang række muligheder for professionel og personlig udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Lili Behjat Kristensen på + 45 3079 4143.

Ansøgningsfrist
27. april 2014

Danmark - Hillerød Kvalitetssikring

Vacant positions posted in English

Date posted Job title Location Category
25-Apr-2014 Sr. International Trial Manager
Do you want to make an impact? In this job, a high number of people worldwide depend on you to develop the world’s best diabetes treatments. If you find challenges like this exciting and inspiring, then we may ...

Sr. International Trial Manager

  • Research & Development, Trial Manager
  • Denmark - Søborg

Do you want to make an impact? In this job, a high number of people worldwide depend on you to develop the world’s best diabetes treatments. If you find challenges like this exciting and inspiring, then we may have just the right job for you.

About the department
Clinical Operations, Semaglutide & Oral GLP-1 is looking for a Senior International Trial Manager to join us. We are an area of more than 40 highly skilled and ambitious colleagues responsible for the planning and execution of clinical trial activities in accordance with the Clinical Development Plans within diabetes. The scope of our activities is phase 2 to 4 clinical trials which we conduct in collaboration with our Novo Nordisk affiliates. Our environment is characterised by a vast global network with interesting and challenging assignments, significant responsibilities, and continuous personal and professional development.

The job
As Senior International Trial Manager you will be responsible for timely planning, execution and finalisation of clinical trials, using your operational and therapeutic experience. You will coordinate trial management activities in a proactive fashion through clear communication and good team work. As a member of the Study Group/International Study Group you will organise and execute team meetings and ensure the involvement of relevant stakeholders for decision making. You have a structured and analytical approach during development of critical trial documents, and at the same time you have an eye for important details while keeping the overview. You are able to digest complex data output and to evaluate the adequate levels of quality in all you do. Finally you work in an independent manner and assume significant responsibilities. By joining us you will get the opportunity to further develop your competencies within trial management in an international headquarter environment. This position covers a temporary 12 months vacancy. (Maternity leave)

Qualifications
You hold a MSc in Natural Science or equivalent with at least 5 years of experience in trial management related positions and with significant project management responsibilities. You have a broad knowledge of clinical trial methodology and our ideal candidate will have experience in execution of clinical cardiovascular outcome trials. A quality mind-set is a must together with a clear focus on meeting deadlines, communicating effectively and knowing how to prioritise between different tasks in a dynamic environment. You are a dedicated team player with a high degree of flexibility and cross-cultural awareness who inspires trust amongst colleagues and partners. Proficiency in written and spoken English is essential.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please call Benedikte Lertoft on + 45 3079 2893.

Deadline
15 May 2014.

Denmark - Søborg Research & Development, Trial Manager
25-Apr-2014 Internship in Biopharm Formulation Development
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Biopharm Formulation Development

  • Student and Internships
  • Denmark - Gentofte

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Department Biopharm Formulation Development is part of CMC Injectable Protein Formulation in R&D. The department is responsible for formulation development of new biopharmaceutical drug products - primarily soluble and freeze-dried injectables of new therapeutic proteins and monoclonal antibodies. We are involved in development and research projects mainly within haemostasis and inflammation.

The job
During your internship, you will be involved in developing stable protein formulations with optimal biopharmaceutical characteristics. You will work in a team and design, perform, interpret and report studies on our drug product - hereby generating pharmaceutical documentation for internal and external use. You will have the opportunity to interact with a wide variety of internal stakeholders, e.g. analytical development, production pilot plant, quality assurance and regulatory affairs.

Qualifications
We are looking for an intern who is passionate about protein chemistry and formulation development of biopharmaceutical drug products. You are currently studying on your master’s degree in pharmacy, biochemistry, chemical engineering or other relevant scientific discipline. We expect candidates to thrive in a busy environment and bring a can-do attitude. Fluency in both oral and written English; ability to manage many project tasks in parallel (with supervision); sound personal judgment; and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 1 Sept 2014

Contact
For further information, please call Malin Gustavsson on + 45 3079 4524.

Deadline
2 June 2014.

Denmark - Gentofte Student and Internships
25-Apr-2014 QA Chemist
Do you want to be part of Quality Assurance and ensure a high level of quality of Novo Nordisk’s insulin products and hereby make a difference for thousands of people? In QA Finished Products (FP) we are lookin...

QA Chemist

  • Quality
  • Denmark - Hillerød

Do you want to be part of Quality Assurance and ensure a high level of quality of Novo Nordisk’s insulin products and hereby make a difference for thousands of people? In QA Finished Products (FP) we are looking for an experienced and ambitious QA chemist, with a desire to work in our FP production in Hillerød.

QA Team Member with drive and a positive mindset

About the department
The new position is an expansion so that we are ready to ensure the quality level in 2014. You will join a dynamic department of 39 highly dedicated employees, divided into three teams all working with quality assurance of our insulin products.

You will become part of a team with an informal relation, good humour and where we take care of each other, and in that way you will rapidly, as a new employee, become a part of the team. We appreciate that you take responsibility as a QA colleague and has a positive mindset toward new challenges.

The job
The team is responsible for assuring that systems and processes in relation to FlexPen® production and the Quality Control (QC) area are in compliance with GMP requirements, and at the same time, we act as compliance support to our production teams.

We work in a fast pace and our key tasks are batch review and approval of all types of GMP documentation; such as batch, change requests, non-conformities and validation reports - all this with the common goal of releasing insulin products to our customers.

On top of that, QA is an important player at internal audits and external authority inspections, where you are expected to participate and present data when needed.

In this fast paced and dynamic environment, prioritisation can quickly change, whereby no days are the same and you will constantly be challenged, both in regards to the complexity of the tasks but also on tight deadlines.

Being a new member of the team, you will undergo a structured and individual training program with one of your colleagues acting as the trainer, and you can expect increasingly more responsibility.

Qualifications
You hold an academic degree, e.g. pharmacist, veterinarian, biochemist, or similar with minimum 1 year of relevant GMP experience or work experience from the pharmaceutical industry and it will be an advantage if you are a Qualified Person (QP).

Most importantly; you thrive in a fast-paced environment where you naturally take the lead and set directions in order to achieve business goals and at the same time you never compromise on quality, authority demands or deadlines. You are structured and a good coordinator and thrive with and are able to work on various tasks simultaneously, and know how to prioritise between different quality tasks - All this with a positive mind-set and team spirit.

Finally, you are fluent in Danish and English – written as well as spoken.

Feel free to submit your job application, as quickly as possible, in either English or Danish.

You can learn more about working as QA in Novo Nordisk by clicking on this link: www.novonordisk.com/careers/QA

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Heidi Bisgaard Jensen on phone + 45 3075 3147.

Deadline
12 May 2014.

Denmark - Hillerød Quality
24-Apr-2014 Intern
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Intern

  • Student and Internships
  • Denmark - Søborg

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You get the opportunity to join an international, high performing team with a variety of backgrounds (project management, communication, marketing, medicine and international business). We use our differences to create novel ideas and high-quality solutions. In Strategic Operations, we develop strategy and processes for Medical Affairs and drive engagement planning and medical education for Key Opinion Leaders & Health Care Professionals. Moreover, we collaborate with key affiliates and stakeholders to ensure continuous improvement of the Medical Affairs function globally and strive for excellence in all we do.

The job
As an intern in Global Medical Affairs Strategic Operations you will take part in various projects and day-to-day tasks. You will support a medical team in Global Medical Affairs with the optimisation of business processes. You will be responsible for updating a control room/dash board as well as preparing management status reports for some of our key brands to ensure effective tracking of medical activities and key performance indicators. You will be involved in the planning and execution of external medical education (meetings, support material) and internal training (eLearning) in which you will interact with vendors and internal stakeholders. Finally you will be supporting team members on ad-hoc tasks, etc. You will have plenty of opportunities to influence the projects you will be involved in.

Qualifications
We are looking for an intern who is passionate about project management and effective communication. You are currently studying on your master’s degree in business, communication, or other related fields. You already have some experience with cross-functional project management either in a work or academic setting. You are fluent in both oral and written English, you are able to manage several projects at the same time and take a methodical approach to your work and tasks, but demonstrate flexibility when priorities change.

In addition, you bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you have excellent interpersonal skills and a professional and personal impact that is reflected in your desire to take initiative and responsibility for your projects.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 15th August 2014

Contact
For further information, please contact Marta Anglada Planagumà + 45 3079 8431.

Deadline
2 June 2014.

Denmark - Søborg Student and Internships
24-Apr-2014 Law student
Pharma Law team in Corporate Legal at Novo Nordisk A/S is seeking a Law Student for paralegal tasks for approx. 15-20 hours per week, under a contract until end of December 2014 (with possibility of extension)....

Law student

  • Legal
  • Denmark - Bagsværd

Pharma Law team in Corporate Legal at Novo Nordisk A/S is seeking a Law Student for paralegal tasks for approx. 15-20 hours per week, under a contract until end of December 2014 (with possibility of extension).

About the department
The Pharma Law Team is located in Novo Nordisk’s headquarters and is comprised of 9 lawyers. The department is part of Novo Nordisk’s Global Legal organisation which employs more than 100 lawyers at more than 20 locations throughout the world. We provide legal advice within a broad range of areas including non-clinical development, device development, pilot production, clinical development, product registration and approval, manufacturing, marketing, distribution and sale, quality and product safety.

The job
This position offers a great opportunity to an ambitious and talented law student located in Denmark interested in obtaining early insights in a broad legal field.

You will work closely with lawyers in the Pharma Law team in Corporate Legal, assisting them in providing legal services to a dynamic and expanding group of international companies and have therefore the chance to get experience and develop competencies in contract law, pharma and regulatory law as well as compliance matters.

The primary working language is English, and most assignments have international aspects.

The work place will be in Bagsværd, Denmark.

Your primary tasks will be supporting lawyers in various legal assignments including contract and document review, legal research as well as administrative tasks.

Qualifications
You are a law student in Denmark and you have solid professional qualifications including at least two years behind you at Law School. You have basic knowledge of Danish and/or international contract law.

You have solid English language skills (preferably also Danish) and you are familiar with the use of IT, including Microsoft Office.

In addition, you are reliable and able to work independently, you are helpful, effective and flexible, and have a good sense of humour.

Please forward your application online via www.novonordisk.com/careers. Please mark your application “21006BR Law Student”. Please remember to enclose exam papers or transcripts of marks, and other relevant documentation.

Please note that all applications should be in English and interviews will be conducted in English.

Contact
For further information, please call Elena Hilligsøe, on + 45 3079 4071 and Mathias Zadrazil on + 45 3075 0512.

Deadline
7 May 2014.

Denmark - Bagsværd Legal
24-Apr-2014 OHS Consultant - Ergonomics
In this job, you will be part of an organisation that supports the rapid global growth of Novo Nordisk, and provides a healthy and safe working environment for all. If you find challenges like this exciting and...

OHS Consultant - Ergonomics

  • Human Resources
  • Denmark - Bagsværd

In this job, you will be part of an organisation that supports the rapid global growth of Novo Nordisk, and provides a healthy and safe working environment for all. If you find challenges like this exciting and inspiring, you may be our new OHS Consultant – Ergonomics

About the department
The job is located in Corporate Occupational Health and Safety (COHS) which is a corporate staff function and a part of Corporate People & Organisation situated in Bagsværd. COHS is Novo Nordisk's Centre of Excellence in the field of global occupational health and safety with 28 dedicated colleagues within ergonomics, psycho-social and technical working environment. COHS’s role is to inspire and support the OHS work throughout the global organisation, enabling line of business to realise Novo Nordisk’s OHS ambitions by providing easy-to-use guidance, tools and data.

The job
We offer a challenging position with a two-folded responsibility;

Firstly, you will be driving the corporate strategy on ergonomics in Novo Nordisk. This will be done through cross-functional projects. You will develop and implement initiatives within ergonomics in close collaboration with stakeholders in the organisation. This involves providing solid data and intensive stakeholder management as well as developing and implementing easy-to-use guidance, standards and tools to the organisation and sharing better practice across the organisation globally within ergonomics. In addition you will support senior management decisions on implementing corporate initiatives that allow for local adaption.

Secondly, you’ll provide both general OHS counselling to the global organisation and consultancy within the field of ergonomics. Your counselling will be based on your expertise knowledge, regulatory requirements, good practice and Novo Nordisk’ values.

Qualifications
You hold a bachelor/candidate degree within workplace ergonomics combined with international project management experience. You have strong analytical skills and have demonstrated the ability to conceptualise and implement cross organisational initiatives in a global company.

At the same time you strive to support local management’s ability to keep the business running smoothly. You are able to document your business accomplishments via senior management references.

You have very strong communication skills and can provide strategies at a corporate level and also develop hands-on tools for the OHS organisation. Your experiences allow you to turn complex matters into simple solutions with a strong stakeholder management focus. As a person you are result-oriented and structured - and your commitment is catching. You have a high level of drive, initiative, empathy and persistence and work well in a dynamic environment.

English is our corporate language, and hence it is a prerequisite that you speak and write English fluently. You work comfortably in MS Office (experienced in PowerPoint). It is also important that you approach tasks and colleagues with a positive attitude, energy and good humour.

At Novo Nordisk, decisions and actions are based on their impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please contact Nina Gylche Møller at + 45 3079 4756.

Deadline
25 May 2014.

Denmark - Bagsværd Human Resources
23-Apr-2014 2 years post doc position at Baker IDI, Mark Cooper
International post-doctoral position for a highly skilled scientist is available in the department of Diabetic Complications Biology, Novo Nordisk in collaboration with Baker IDI Heart and Diabetes Institute, M...

2 years post doc position at Baker IDI, Mark Cooper

  • Research & Development
  • Denmark - Måløv

International post-doctoral position for a highly skilled scientist is available in the department of Diabetic Complications Biology, Novo Nordisk in collaboration with Baker IDI Heart and Diabetes Institute, Melbourne, Australia.

About the department
The Diabetic Complications Biology (DCB) department is offering an international post-doctoral fellowship to a highly motivated, innovative and goal-oriented candidate. DCB is part of the Diabetes Research Unit (DRU), which is a research centre providing drug candidates for changing diabetes and is an integrated research unit of Novo Nordisk. The DCB department is specifically involved with the identification and biological validation of novel therapeutic targets within renal and retinal diabetes complications.

The Job
The project will focus on the potential role of glucagon-like peptide (GLP)-1 in protecting renal cells from cellular stress caused by factors, which are involved with the development of diabetic nephropathy. The work will be carried out in collaboration with Dr. Mark Cooper, Baker IDI Heart and Diabetes Institute, Melbourne, Australia. The overall goal is to increase our knowledge of

GLP-1 action in kidney function with a focus on renal cell characterization, signalling, function and survival in diabetes.

The candidate will be employed by Novo Nordisk. Most of the work will be carried out in the laboratory of Dr. Mark Cooper, Baker IDI Heart and Diabetes Institute, Melbourne, Australia and a minor part in the DCB department, Novo Nordisk, Måløv, Denmark. The candidate will be in Melbourne for approximately 18 months starting from early fall 2014.

The start date is June 2014, and the duration of the position is 2 years. The position is funded directly by the DCB department.

Qualifications
This position requires a PhD in biological, medical science or related disciplines. Strong biology and receptor biology skills are required. Experience with primary cell culture, biological signalling assays, qRT-PCR, ELISAs, flow cytometry and other biological assays for measuring cell signalling and cell survival is desirable. Knowledge of GLP-1 biology, kidney function, pathogenesis of nephropathy and diabetes is an advantage. The position requires a global mindset and very good communication skills in English.

At Novo Nordisk, we strive for excellence. Your curiosity, skills, dedication and ambition will help us change lives for the better. We offer you an opportunity to work in an extraordinary, stimulating scientific environment at the Baker IDI and Novo Nordisk.

Contact
For further information, please call Christopher Mayer at +45 3075 9944 or Anette Nielsen at +45 3075 7025.

Deadline
7 May 2014.

Denmark - Måløv Research & Development
23-Apr-2014 Internship in FlexTouch Production Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in FlexTouch Production Support

  • Student and Internships
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You get the opportunity to join a high performing team in Hillerød, Denmark, responsible for keeping our assembly and packaging production lines running and in compliance with the numerous requirements in medical production. In close collaboration with supporting departments in our area we perform the changes needed on the lines either for closing quality gaps or improving the performance of the lines. Some changes require validation of the equipment after implementation and we are responsible for the coordination, execution and the update of technical documentation that these validations contain. One of the main pillars in medical manufacturing processes is the procedures that tell you how to perform tasks. We are responsible for the maintenance procedures which are used by our technicians and the operating procedures which are used our line operators.

The job
You will assist the process responsible and supporters in the team with keeping the written procedures and other documents updated. In your tasks you will be handling different stakeholders such as the operators and technicians that use the procedures and our quality assurance people who approve most of our work. You will be working with Word and Excel as many of our documents are in this format. You will also get experience with internal systems when you need data from the lines or other documentation. You will be a part of the daily business processes and get experience in working alongside a pulsating medical production in Novo Nordisk.

Qualifications
We are looking for an intern who is passionate about details and quality processes. You are currently studying on your degree in mechanical engineering, production engineering or similar. We expect candidates to be service minded, thrive in a busy and challenging environment and bring a can-do attitude. Fluency in both oral and written English; ability to manage a large volume of tasks (with supervision) and plan the activities; and excellent interpersonal skills are required. You are an outgoing person with a strong personal drive and dedication. You are known as a person taking responsibility for your tasks and you show persistence and creativity, especially when meeting obstacles. In addition, you bring a healthy sense of humour to your work – even when the pressure is on.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01-08-2014

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Jacob Dam Sørensen on + 45 3075 2354.

Deadline
2 June 2014.

Denmark - Hillerød Student and Internships
23-Apr-2014 Internship to leadtime project in Quality
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship to leadtime project in Quality

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
As our new trainee you will be part of our well-functioning team, dept. 720, placed in Bagsværd. Our team consists of 6 dedicated colleagues, and together, we are responsible for quality processes, such as incidents, Change Control, Corrective- and Preventive Actions and audits/inspections.

The team values professional sparring and you can look forward to entering into an energetic and positive working environment where cooperation is a keyword.

The job
You responsibility will be find out the best way to create a system where we can measure our lead-time in the Quality area.

We want to measure our own lead-time when we handle incidents, Change control cases, batch releases, customer complaint etc.

You will have a coach and you will be introduced to how we work to trim our processes and make our better in Novo Nordisk A/S.

Qualifications
You are well-organised, independent and have a strong analytical sense.

A flair for systems an especially Excel is a demand.

You take pride in planning and improving our high standards including ensuring that new ways of working are implemented smoothly.

You are attracted by the opportunity to use your quality skills in a highly complex site and ever changing working environment.

At Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 6 months.

Contact
For further information, please contact Iben Hjelmsø at + 45 3075 3631.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
23-Apr-2014 Clinical Research Associate
We currently have vacancy for an experienced Clinical Research Associate (CRA) for a fixed term contract of 1,5 year reporting to the Head of Clinical Research in the Danish affiliate. ...

Clinical Research Associate

  • Clinical
  • Denmark - Greater Copenhagen area

We currently have vacancy for an experienced Clinical Research Associate (CRA) for a fixed term contract of 1,5 year reporting to the Head of Clinical Research in the Danish affiliate.

About the department
The job is located at the Danish affiliate of Novo Nordisk based in Ørestad. As CRA you will be part of a Clinical Research team of 12 dynamic colleagues dedicated for clinical research.

The job
The main purpose of the role is to conduct high quality clinical trials within the scheduled time in accordance with protocols and the company’s policies and Standard Operating Procedures (SOPs), National Regulations/requirements and ICH GCP requirements.

Responsibilities of this exciting and challenging role at Novo Nordisk include all trial related activities required for proper conduct of clinical trials from site selection to site closure (e.g. site selection, approvals from authorities, site initiation, monitoring and SDV, safety handling, trial supplies management, data cleaning activities, site closure and archiving).

You will liaise closely with colleagues within the Clinical Research Team, the Head of Clinical Research and our company Headquarters throughout the trials to ensure milestones are achieved. This role requires travelling.

Qualifications
The ideal candidate will be educated to graduate level or equivalent and have GCP certification. You have previous experience of monitoring clinical trials in accordance with ICH GCP methodology and good knowledge of the clinical trial methodology and up to date knowledge of the clinical trials environment. You have successfully applied for and run clinical trials in Denmark. Good IT skills are essential and diabetes therapy area knowledge is desirable. As a person you are result oriented, structured and flexible and you like to work in teams as well as independently. You must be fluent in both Danish and English and have a valid driving licence.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.”

Contact
For further information please call Ulla Soelberg on + 45 3075 3238.

Deadline
14 May 2014.

Denmark - Greater Copenhagen area Clinical
22-Apr-2014 Intern
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Intern

  • Marketing
  • Denmark - Søborg

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You have the opportunity to join an international, high performing team responsible for generating customer insights (being physicians and patients) and utilise the insights and knowledge to impact brand strategy and tactics development across Novo Nordisk diabetes and biopharm portfolio. In close collaboration with key internal stakeholders in Global Marketing brand teams and affiliates, we execute market research projects, and conduct anonymised, patient level data analysis. We advocate a customer centric approach in strategy and tactic formulation, being an integrated partner for Global Marketing brand teams.

The job
You will support Global Customer Insights Managers in the Customer Insights team in anonymised, patient level data analysis. In this role, you will be programming in SAS base, working with data mining, generating market insights and communicating the insights to relevant internal stakeholders. You will also work alongside Global Customer Insights Managers and Global Product Managers, in analysing market dynamics and providing input for brand strategy and tactic development.

Qualifications
We are looking for an intern who is passionate about analysis and communication and working in the pharmaceutical industry. You are currently studying your master’s degree in life science (Mathematics or Statistics), economics, marketing or other relevant fields and have demonstrated strong project management and analytical skills through your study. Ability to analyse large quantities of data and design reports using Excel, fluency in both oral and written English and excellent interpersonal skills are required. Usage of SAS is preferred. We expect the candidate to be goal oriented, thrive in a busy environment and bring a can-do attitude.

You have a strong personal drive and dedication. You have the ability to digest comprehensive market and customer information and findings into concise insight and have the ability to communicate it to internal stakeholders. You must have strong work ethic and willingness to take responsibility for your own learning.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 15.08.2014

Contact
For further information, please contact Wei Sun at + 45 3079 7855 or Patricia Tan at + 45 3079 6525.

Deadline
2 June 2014.

Denmark - Søborg Marketing
22-Apr-2014 Intern to CMC Process Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Intern to CMC Process Support

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
The internship is in CMC Process Support, a department in CMC Supply responsible for lean and statistical support across the organisation. In terms of lean, in Novo Nordisk called cLEAN®, the department is responsible for building competences through our cLEAN® Academy and driving strategic improvement projects across CMC Supply. The other main responsibility is statistical support to our development processes and building statistical competences across the CMC Supply.

The job
You will primarily support two project managers in their role of driving strategic improvement projects. In this role you will conduct analyses, prepare business cases and support improvement workshops as well as implementing and anchoring solutions. You will also be part of the training team where you will train colleagues across CMC Supply within our field of expertise.

Qualifications
We are looking for an intern who is passionate about lean/SixSigma and has interest in and flair for data analysis. You are currently studying on your master’s degree in Supply Chain Management, engineering or other relevant field. General knowledge of the pharmaceutical industry or experience with improvement methodologies is preferred. Our preferred candidate has through previous student’s job(s) demonstrated to be service minded, ambitious, and thriving in a busy environment. Fluently in both oral and written English and excellent interpersonal skills are required. Danish language skills are a prerequisite.

You are an outgoing person with a strong personal drive and dedication, and your curiosity and ability to quickly assess complex problems makes you capable of generating improvement input to the processes and systems surrounding you. In addition, you thrive in a busy environment and bring a can-do attitude and a sense of humor to work.

Practicalities

Qualification: Students in their first or second year of their master studies

Period: The internship position is a full-time position for 4-6 months (depending on your studies)

Start date: Preferably 01-SEP-2014.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
Please contact Ole Ekelund + 45 3079 1083.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
22-Apr-2014 Internship in Market Access
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Market Access

  • Student and Internships
  • Denmark - Søborg

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You get the opportunity to join an international, high performing team with a variety of backgrounds. Global Market Access is an expanding, international, high performing team of colleagues in Søborg, Denmark, responsible for optimising market access for the continued success of the Novo Nordisk Portfolio. In close collaboration with key internal stakeholders, Global Market Access establishes the strategies and key support tactics in the area of pricing, reimbursement, health economics & outcomes research, value communication, and subsequently supports the implementation regionally and locally.

The job
Professionally you will participate and get experience from working with one or more drug products and therapeutic areas, working on general tasks and learning how to coordinate various aspects of health economic and outcomes assessments for those products. This includes the writing of technical reports and preparing presentations to internal stakeholders. Along with on the job training, candidates will be assigned a mentor and expected to deliver a project and a related presentation to a diverse audience at the end of the internship. Successful candidates must be a high performer with an interested in the interactions between science and policy, wants to work with dynamic people and contribute to a changing environment. On the personal side, you will gain experience with multiple stakeholder management, execute through and with others, get global insights and you will have opportunities for multi-functional interaction.

Qualifications
You are a Masters student in economics, econometrics, pharmacoeconomics, outcomes research, public health, pharmacy administration or related field with solid technical skills. You must possess effective oral and written communication skills, you are fluent in both oral and written English, and must be a self-starter with the ability to maintain high productivity with supervision. Finally, you have excellent interpersonal skills and a professional and personal impact that is reflected in your desire to take initiative and responsibility for your projects.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01 September 2014

Contact
For further information, please call Agathe Le Lay on +45 3079 3956.

Deadline
2 June 2014.

Denmark - Søborg Student and Internships
22-Apr-2014 Experienced Senior Quality Professional
Do you want to influence a high level of compliance with GMP / quality management system (QMS) requirements, ISO standards and Novo Nordisk procedures? Then you might be the right person for the job as Senior Q...

Experienced Senior Quality Professional

  • Quality, senior position
  • Denmark - Hillerød

Do you want to influence a high level of compliance with GMP / quality management system (QMS) requirements, ISO standards and Novo Nordisk procedures? Then you might be the right person for the job as Senior Quality Officer in Device Manufacturing & Sourcing (DMS).

About the department
As our Senior Quality Officer you will be part of our QMS support team in DMS. The team reports directly to the Quality VP in DMS. The team is responsible for cross functional quality activities in DMS, such as coordination and follow-up on audits and inspections, GMP training, reporting on quality KPI’s, QMR and the CAPA system. The team provides cross functional QA services and coordinates quality assurance initiatives and projects.

The job
You will play a key-role in setting directions and standards for the way DMS implements and maintains continuous improvements and harmonisations into the QMS as well as drive or participate in quality projects and initiatives coming out of our Product Supply organisation to ensure an effective implementation in DMS.

You will be part of DMS Quality management team and also provide QMS support to DMS management. It is your responsibility to report and follow-up on quality activities and topics at monthly management meetings and you will be Process Responsible for one or more quality processes e.g. the QMR process and GMP training, with a direct possibility to influence the compliance level in DMS.

Ensuring a high level of inspection readiness you are responsible for coordination, execution and support follow-up on audits and inspections.

Further, it is your responsibility to ensure compliance alignment and knowledge sharing between DMS and our Product Supply organisation by participating in QA cross and compliance groups as DMS representative.

Qualifications
You hold an academic degree as engineer or pharmacist and have preferable +5 years of experience from a pharmaceutical or medical device industry where you have gained a solid and up-to-date knowledge of quality, GMP and ISO requirements. It is important that you have an in-depth understanding of QMS requirements and have been working with interpretation, implementation and training in new QMS requirements. Further, we expect you to have experience as lead auditor and with project management.

As a person you are enthusiastic, committed and proactively seek the information you need and have hands on approach. You are analytical and systematic in your approach. You are able to see things in larger perspectives and experienced in working and communicating with people at all levels in the organisation and across organisational boundaries. You use your excellent cooperation skills when you manage your stakeholders both in- and externally to ensure solutions that will meet both requirements and stakeholders’ interest.

You are service-minded, enterprising, independent and persistent. In DMS we are determined to be best in class and it is therefore important that you are able to see opportunities instead of limitations without compromising a high level of compliance.

Finally, you communicate fluently both written and spoken in English.

At Novo Nordisk, decisions and actions are based on their impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please call Jacob Stenmann Valsborg at +45 3075 4798.

Deadline
27 April 2014.

Denmark - Hillerød Quality, senior position
22-Apr-2014 Internship in Supply Chain Controlling
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Supply Chain Controlling

  • Student and Internships
  • Denmark - Måløv

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Clinical Supplies Supply Chain Planning (CS SCP) is a key member of Research and Development and is vital in bringing new drugs to market. In CS SCP, we have a unique understanding of the combination of drug development and supply chain management. Our main and most important task is to ensure that trial products are available on time and in the right quality and quantity for all clinical trials conducted by Novo Nordisk. We work in close collaboration with our many stakeholders worldwide. In order to meet the ambitious goals of Novo Nordisk within diabetes, haemophilia and other chronic diseases, we are furthermore working towards shortening lead times, optimising the use of resources and reducing our product waste by means of various LEAN tools. We are almost 40 people in CS SCP and are located at Novo Nordisk site Måløv. The department is divided into three teams (Supply Planning 1 and 2 and Temperature Control & Material Planning).

The job
Our clinical trial activity will be high in the coming years and to support this development, we are looking for an intern to support our work with trial budgets and controlling of the costs related to the execution of clinical trials. As this activity represents a significant cost to Novo Nordisk we are continuously seeking to identify and implement process improvements.

As an intern in Clinical Supplies Supply Chain Planning, you will have both individual analysis tasks and participate in projects with colleagues from the department. You will support your colleagues with different tasks of varying character both day to day operational tasks and tasks which will improve their daily work particularly related to the financial part of driving the trials.

Qualifications
We are looking for an intern who is passionate about finance and supply chain management. You are currently studying on your master’s degree in finance, supply chain or other relevant field. You have strong analytical skills, a strong quality mind-set, communicate effectively, meet deadlines, and approach tasks in a structured way. You are a dedicated team player who inspires trust amongst colleagues and partners. You have a positive attitude to challenges and see continuous improvement as a natural part of your job. You have excellent computer skills - in particular you are an experienced MS Excel user. You are fluent in written and spoken English.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 1 September 2014

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Stine Mørch, + 45 3079 9847.

Deadline
2 June 2014.

Denmark - Måløv Student and Internships
22-Apr-2014 Global Project Manager
Global Project Manager – an international job with touch points to colleagues and external contacts from most of the world! ...

Global Project Manager

  • Project Management
  • Denmark - Søborg

Global Project Manager – an international job with touch points to colleagues and external contacts from most of the world!

About the department
A unique position as Global Project Manager in Study Programmes, which is part of Global Medical Affairs in the Novo Nordisk HQ Denmark, is open for immediate placement by a candidate with a proven track record within Project Management and Marketing/Communication and/or Clinical research.

The job
As Global Project Manager you will become a key member of a growing global team with experienced project managers from many different countries and backgrounds. Our team develops and implement supporting initiatives to ensure successful recruitment and retention of patients in our large long lasting clinical studies. We call it Scientific Recruitment & Retention Programmes (SRR).

The key tasks:

Development and roll-out of patient recruitment and retention tools for affiliates to implement

Project manage advisory boards/expert panels and project manage the planning and execution of related meetings

Develop and implement scientific communication and education materials as part of the trial SRR programme

Secure proper internal knowledge and motivation of Novo Nordisk colleagues via development and implementation of communication packages, meetings and training

At the global level you will become a key contributor to the global activities, ensuring that the SRR programme accommodates the needs and requirements of affiliates involved in the study.

At the global and local level you will engage with multiple and diverse cross-functional stakeholders and several external vendors. You will also take active part in key activities both at the global and local level. 30-40 travel days a year should be expected.

As Study Programmes is a relatively new function in the company you will have ample opportunity for influencing our deliverables, enhancing our processes and identify new ways of achieving goals.

Qualifications
You have a business or science degree combined with min 5 years work experience from the pharmaceutical industry, preferably in both global and local roles.

You have broad experience with planning projects and implementing them successfully. You are skilled in developing and executing communication concepts, and experience from a pharmaceutical brand team is also an asset. You are able to work on multiple tasks in parallel and cope well under time pressure while maintaining your good sense of humour.

You have personal drive and are enthusiastic, energetic, confident and able to work on multiple tasks to meet personal and team goals.

You are comfortable working in a dynamic environment and have excellent interpersonal skills and a track record of successful collaboration and influencing multidisciplinary stakeholders from multiple countries.

You have good communication and presentation skills as well as strong command of English both written and spoken.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Jan Kildeskov at + 45 3079 0069.

Deadline
13 May 2014.

Denmark - Søborg Project Management
22-Apr-2014 Internship in Process Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Process Support

  • Production
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Device Manufacturing & Sourcing is focused on introduction of moulded components for medical devices, maturation of the production setup to excellence and sourcing the components to sister sites abroad. The area is at a high development pace with increasing production volumes which is directly impacting the Mould Pipeline & Validation (MPV) team, responsible for ordering and approval of injection moulds for plastic parts for prefilled devices produced internally in Hillerød DK and on various production sites worldwide.

The job
You will be working in a dynamic team with 10 other dedicated employees in Hillerød. You will support the team with various data analysis and LEAN Six Sigma tasks to ensure the right reporting tools and performance measurement and management systems are in place. You will drive workshops to optimize workflow and collect and analyse data to estimate workload forecast and thereby help the team in ensuring the correct number of resources going forward. You will analyse, plan and evaluate business- and production related challenges from more than one perspective and be part of the entire process life cycle from idea collection and KPI setup to implementation and continuous improvement.

Qualifications
You are currently studying on your master’s degree within engineering, process improvement, operation management or another relevant field. Basic knowledge of LEAN six sigma and related key methodologies is preferred and you should be confident with various data analysis.

You are an outgoing person with a strong personal drive and dedication and used to create results through projects. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you bring a can-do attitude and have an excellent overview, a structured mind-set and a dedicated way of working as well as very good communication skills. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: Aug/Sep 2014

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Laura Sørensen +45 3075 0463.

Deadline
2 June 2014.

Denmark - Hillerød Production
22-Apr-2014 Internship - Passionate Mechanical Engineer
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship - Passionate Mechanical Engineer

  • Student and Internships
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Device Research & Development is an area within Global R&D, responsible for the development of medical delivery systems for self-treatment within all business areas of Novo Nordisk A/S. Device Research & Development has a long and outstanding track record of developing the best, most innovative and widely-used injection systems in the world. You will join an international team of 12 highly skilled engineers and designers and we are located at a state-of-the-art R&D facility in Hillerød, Denmark.

The job
You will get the opportunity to become an integral part of an ambitious project team. The team is responsible for the development of innovative mechanical injection devices, covering every aspect from conceptual design to Design for Manufacturing. As a team member, you will get the chance to work with conceptual ideation, prototyping, mechanism design, structural and theoretical analysis and CAD modelling.

Qualifications
We are looking for an intern who is passionate about innovation and development. You are currently studying towards a master’s degree in engineering, preferably within mechanical engineering. Knowledge about mechanism design, structural analysis and CREO is an advantage. We expect candidates to be service-minded, thrive in a fast-moving development environment and bring a can-do attitude. We are looking for a team player with sound personal judgement and excellent interpersonal skills. Proficiency in oral and written English is essential.

You are a self-motivated person with a desire to take ownership and initiative in every aspect of your work. You are curious and inventive. In addition, you thrive in a busy environment and bring a constructive attitude – even under pressure. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

At Device Research & Development we use our skills, dedication and ambition to help people manage their diabetes. You will get the opportunity to be part of an innovative R&D environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for approx. 6 months.

Start date: August 2014.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Salim Bouaidat on + 45 3075 8658 or Lars Bom on + 45 3075 1324.

Deadline
2 June 2014.

Denmark - Hillerød Student and Internships
20-Apr-2014 IT Category Manager
Do you have a strong business mind-set and are you looking for a job with the possibility to utilize and further develop your skills and competences within negotiations, contracting, supplier management, catego...

IT Category Manager

  • Sourcing
  • Denmark - Bagsværd

Do you have a strong business mind-set and are you looking for a job with the possibility to utilize and further develop your skills and competences within negotiations, contracting, supplier management, category management and stakeholder management?

About the department
Corporate Procurement is, in close cooperation with affiliates and stakeholders, responsible for purchasing, sourcing and contracting of the global indirect spend in Novo Nordisk. Corporate Procurement has more than 100 employees and is a part of Finance. This position is in the IT Sourcing Team. We are commercial experts with responsibility for leading the sourcing processes, negotiations and Category Management.

The job
Your will have the role as Lead Negotiator for IT projects and as Category Manager for certain IT categories. You will have to manage and align with stakeholders to prepare and adhere to negotiation strategies, category strategies and commercial sourcing processes. As Category Manager you will be the driving force in developing and implementing category strategies for your categories and lead Supplier Relationship Management. You will be a part of an enthusiastic group that sets high standards and individual targets, but achieves them as a team.

Qualifications
You have at least 5-7 years relevant sourcing or contracting experience and a track record in delivering above average results. You may have experience from sourcing or selling within IT categories. You have strong strategic, reasoning, and analytical skills. You have the ability to effectively plan, prioritise and execute. You are robust, self-motivating, very result oriented, always raising the bar for yourself and encouraging your peers to follow. You communicate and sell your ideas effectively and have the ability to work with various stakeholders, colleagues, and management. You are fluent in English. You probably hold a relevant Master’s degree in Business, Law or IT.

At Novo Nordisk, decisions and actions are based on their impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please call Jan B. Lausten on + 45 3075 7819.

Deadline
12 May 2014.

Denmark - Bagsværd Sourcing
16-Apr-2014 Team leader in Purchasing Service Centre (Indirect Spend)
Are you looking for new challenges? Now you have an exceptional opportunity. We are looking for a visionary and result-oriented team leader of the Purchasing team in the Purchasing Service Centre. If you know h...

Team leader in Purchasing Service Centre (Indirect Spend)

  • Finance
  • Denmark - Bagsværd

Are you looking for new challenges? Now you have an exceptional opportunity. We are looking for a visionary and result-oriented team leader of the Purchasing team in the Purchasing Service Centre. If you know how to combine long-term aspirations with needs to deliver on a daily basis you might be the ideal candidate for this position.

About the department
The Purchasing Service Centre (PSC) is responsible for the purchasing process for indirect spend in Novo Nordisk. We work closely together with our procurement colleagues in the Corporate Procurement organisation, Global Service Centre in Bangalore, our internal customers being the employees in Novo Nordisk, and the external suppliers.

The job
You will be responsible for leading and developing the purchasing and the operations in a team of 12 dedicated employees.

More specifically the team handles purchasing orders within goods and services. To successfully accomplish the task it requires good relationship to all stakeholders, may it be the procurement category managers, the customers in Line of Business, the suppliers, external auditors or various departments in Corporate Finance.

You will work closely together with the team of leaders in PSC to resolve issues and improve and develop the purchasing-to-pay process.

Qualifications
You have completed a relevant master's degree (e.g. in finance, economics or supply chain) with excellent results. You have at least 3 years of experience in line management including development and performance management of administrative employees. You have strong analytical skills and you are fluent in written and spoken English and Danish.

As a person you possess excellent communication and presentation skills and you are able to interact across functions on all levels in the organisation. You have a strong quality mind-set and you are well organized and combine your leadership skills with goal orientation and a tactical approach to problem solving. Additionally, you enjoy working in a dynamic and changing environment and you have a proactive approach to tasks and challenges.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Nicolai Thorborg on +45 3079 5927 or Lars Adrian Møller on +45 3079 5199.

Deadline
1 May 2014

Denmark - Bagsværd Finance
16-Apr-2014 Intern to CMC Business Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Intern to CMC Business Support

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
The internship is in CMC Business Support, a department in CMC Supply responsible for developing and maintaining processes and systems to support the planning of a very ambitious pipeline of drug development projects in CMC Supply. One of the key elements in securing strong operations of a large project portfolio is the CMC Planning project, which is aiming at establishing a solid and transparent process allowing all drug development projects to establish and maintain overviews of the projects material demand and supply situation.

The job
You will get the opportunity to participate in implementation and updates of some of our smaller but important IT systems in CMC Supply. This requires that you familiarize yourself in the system functionality and the user requirements. You will get involved in the creation of test cases, execution of user tests and documentation of the system functionality. Furthermore your tasks will include system description in user guides and creation of training material. For the right candidate the job will also be an opportunity to influence the future integration between the IT systems and the material- project- and financial- planning process.

Qualifications
We are looking for an intern who is passionate about planning processes and systems. You are currently studying on your master’s degree in engineering, Supply Chain Management or other relevant field. Our preferred candidate is service minded, ambitious, outgoing and thriving in a busy environment. Fluency in both oral and written English and excellent interpersonal skills are required. Danish language skills are a prerequisite.

Practicalities

Qualification: Students in their first or second year of their master studies

Period: The internship position is a full-time position for 5-6 months.

Start date: Preferably 01-Sep-2014.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Helle Rasmussen + 45 3075 5021 or Anne Blichfeldt Møller + 45 3079 6982.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
16-Apr-2014 Regulatory Affiliate Supporter
In Regulatory Affiliate Support, we are looking for a Regulatory Affiliate Supporter, as a maternity cover, to join a dedicated group of people working closely together with Novo Nordisk A/S affiliates worldwid...

Regulatory Affiliate Supporter

  • Administrative
  • Denmark - Søborg

In Regulatory Affiliate Support, we are looking for a Regulatory Affiliate Supporter, as a maternity cover, to join a dedicated group of people working closely together with Novo Nordisk A/S affiliates worldwide and Regulatory Affairs product/project groups in headquarters in Denmark.

About the department
Regulatory Affiliate Support is part of Regulatory Operations within Regulatory Affairs, which makes medicine available to patients all over the world by ensuring rapid regulatory approval in all markets. Regulatory Affairs is a fast-changing field, and the 330 employees in headquarters serve as Novo Nordisk’s advocates around the world – and make a meaningful difference to our business.

You will be part of a team consisting of 15 people situated in Søborg, Denmark providing support and services across Novo Nordisk A/S projects and products.

The job
In Regulatory Affiliate Support we are responsible for supplying Novo Nordisk A/S affiliates and product/project groups with additional registration file documentation for submissions to health authorities worldwide.

As Regulatory Affiliate Supporter, you will work as the central point of contact for Novo Nordisk A/S affiliates. Your primary task will be to support with additional documentation such as samples, certificates and statements. Furthermore, management of IT systems to ensure precise update of our product portfolio in collaboration with the Regulatory Operations Team in India will also be part of the job.

The working environment is hectic and very exciting, and no two days are alike. In your daily work you will be collaborating with many different groups of people and it is a necessity that you like and are capable of handling and switching between the many queries coming from our stakeholders.

Qualifications
You have experience from working within Regulatory Affairs or the pharma industry, as well as a relevant background such as pharmaconomist, bachelor in science, laboratory technician, nurse or similar. You are a team-player, have a positive mind-set and a good sense of humour. Flexibility, managing tight deadlines and a sense of details are your strongest assets as well as a quality mind-set. Fluency in written and spoken English is a must.

As a person you are outgoing, proactive and have a strong drive. You find it easy to be in contact with many different cultures and people in various positions, and you have a global understanding and good collaborative skills. You thrive in a busy environment and bring a can-do attitude.

Please submit your application online including motivational letter and CV in English.

In Novo Nordisk A/S it is your skills, your commitment and your ambitions which help us to improve many people’s lives. In return we offer you the opportunity to work with talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please contact Tina Lindquist at + 45 3075 9652

Deadline
4 May 2014.

Denmark - Søborg Administrative
16-Apr-2014 QA Academic for release and development of new API’s
Do you want to unfold your profound QA knowledge and your huge appetite for creating results in a pharmaceutical production environment? If so, please apply for the position as QA Academic in a job that include...

QA Academic for release and development of new API’s

  • Quality
  • Denmark - Bagsværd

Do you want to unfold your profound QA knowledge and your huge appetite for creating results in a pharmaceutical production environment? If so, please apply for the position as QA Academic in a job that includes many different clinical stages of the product development.

About the department
In Chemistry, Manufacturing & Control (CMC) API QA we assure that each and every Active Pharmaceutical Ingredient (API) activity in our development and support projects live up to the cGMP requirements. The development portfolio is expanding and thus we seeking a new colleague to help us support the growth.

We are 32 colleagues in three teams. You will join the Upstream team and have 10 dedicated colleagues. Our mission is to assure that our manufacturing processes, cell banks and intermediates from the upstream API process meet the internal and external requirements. Furthermore we’re responsible for release of API for all of Novo Nordisk’s clinical trials. The production facilities and the development laboratories are located in Bagsværd and Hillerød, and you will move between the different locations and the QA office on a day-to-day basis.

The job
You assure best-in-class quality of our new manufacturing processes and API for clinical trials. Document approval in connection with development, manufacture, stability and release of API for clinical trials as well as maintenance and improvement of the quality system (SOP’s) will constitute some of your daily tasks. In addition, you will participate in our development projects and in close cooperation with your colleagues you identify and contribute to the strengthening our stakeholders’ compliance level and act as a consultant for them.

We operate in a LEAN-dominated environment, and you will have the opportunity to contribute with ideas for improvements and drive the subsequent implementation as well. Working within QA will definitely challenge your professional and individual skills, and you will find that your tasks cover many different clinical stages of the product development.

Qualifications
You hold a Master’s degree in Pharmacy, Chemical Engineering or possess equivalent qualifications besides a strong quality mindset. You have at least 2 years’ experience with GMP, product release, production or quality assurance. As we operate both in a national and an international environment, you must speak and write Danish and English fluently.

You are ambitious and determined on creating world-class results and ensure quality of the highest order. Moreover, you thrive in a role where you use your knowledge and bring your arguments and negotiation skills into play. You are able to adapt but also challenge our way of working so that we constantly improve our methods and processes.

At Novo Nordisk, you will be part of a company respected equally for its financial results and its business ethics. Across geographical, cultural and professional communities we develop and deliver innovative medicines.

Contact
For further information, please contact Lisbeth Voetmann at +45 3075 0530 or Peter Søtofte Elten at +45 3079 8453.

Deadline
4 May 2014.

Denmark - Bagsværd Quality
16-Apr-2014 Internship in Business Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Business Support

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Strategic Sourcing is the central sourcing unit in Novo Nordisk’s Product Supply division, and we are responsible for the strategic sourcing activities related to Novo Nordisk’s worldwide pharmaceutical production sites as well as global management of suppliers. In Business Support we drive cross-unit projects and contribute to value-adding financial, commercial and market intelligence to the other three departments in Strategic Sourcing. You will enter a fast-paced and ambitious environment where we collaborate closely with stakeholders inside as well as outside Novo Nordisk. You will be located in Bagsværd, where 10 competent colleagues look forward to welcoming you.

The Job
As intern in Business Support your job will be to act as support to larger projects in the department. Furthermore, you will be supporting some of our standard reporting processes within quality and compliance. In addition it will be your responsibility to complete various analyses and manage large data sets. You can anticipate varied working days with many different tasks and numerous stakeholders. You will be considered an integrated member of the department and you will receive continuous feedback on your work.

Qualifications
You are currently studying on your master’s degree in International Business, Supply Chain Management, Economics or similar. In any case, you have sharp analytical skills and knowledge about project management. You are expected to have a flair for IT and be a super user of MS Office. To drive your projects successfully (with supervision), you need a structured approach, have a critical eye for details and a mind focused on quality. In addition, you characterise yourself as a flexible person with an unmistakably high level of drive. Good cooperation skills are essential and the ability to work in a complex and dynamic organisation is a prerequisite. Last but not least, you have solid English language skills in speech and in writing.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 1 September 2014

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Lau Brüniche-Olsen +45 3079 0569.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
16-Apr-2014 Internship with focus on Quality improvement, Novo Nordisk
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship with focus on Quality improvement, Novo Nordisk

Learn more about the largest site in Novo Nordisk's global production network using this link www.novonordisk.com/kalundborg-careers

  • Student and Internships
  • Denmark - Kalundborg

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will join our Aspart purification Department – Aspart is Novo Nordisk’s fast acting insulin. We are part of Insulin Manufacturing 1 with a total of 390 people in Kalundborg. You will also be part of our very strong Quality team where cooperation and unity are key words. Novo Nordisk in Kalundborg is a city within the city. The area is situated a good hour from Copenhagen and covers 1,350,000 m2, including a private roadgrid. We produce some 50 % of the insulin in the world.

The job
You will be part of our quality organisation – a very important cross-functional group working together with a lot of colleagues throughout the organisation. You and the rest of the quality group are key persons to ensure that we pass important inspections from the authorities – hereby also ensure that new quality standards and requirements are implemented throughout the organisation. You are working cross-organisational to prepare new standards to ensure standardised work. Through daily sparring with production and support functions you are setting direction on quality – working closely together we obtain new quality standards.

Qualifications
We are looking for an intern who is passionate about Quality and production processes. You are currently pursuing a master’s degree in Chemistry, Biotechnology, pharmacy, public health, Engineer or other relevant field.

We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. Ability to manage a large volume of projects and assignments (with supervision); sound personal judgment; and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

In combination with your natural interest in others and your ability to put yourself in charge you master the fine art of knowing when to compromise and when to stand firm. You are able to independently plan and drive your own tasks. If you do not already master Excel, you demonstrate your fast learning capabilities here as well.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01-08-2014

Contact
For further information, please call Ane Winther Borch on + 45 3079 8487.

Deadline
2 June 2014.

Denmark - Kalundborg Student and Internships
15-Apr-2014 Department LEAN Coordinator – production, drive and engagement
Do you have the drive to work closely with team leaders and employees on the production floor, using your LEAN mind-set and tools to improve how we deal with our daily challenges? If yes, then we have the job f...

Department LEAN Coordinator – production, drive and engagement

  • Production
  • Denmark - Hillerød

Do you have the drive to work closely with team leaders and employees on the production floor, using your LEAN mind-set and tools to improve how we deal with our daily challenges? If yes, then we have the job for you.

About the department
The department consist of 2 teams with approximately 40 employees in total. Our purpose is to ensure packaging of our Flexpen© and make sure that we deliver as promised when it comes to quality, compliance and deadline. We also deliver support to the packaging production and ensure 24/7 production time.

The job
As Department LEAN Coordinator you will report to our department manager and will be part of the department management group. You will also have dotted line to the LEAN Partner for the Vice President. Your main role will be to continuously improve LEAN competencies and support different LEAN activities — all focused on improving stability and quality across our production sites in Denmark.

You will therefore be spending most of your time on the production floor, supporting leaders in development of systems e.g. performance boards, problem solving and process confirmation. Your focus will be to see, solve and follow-up on problems, in a way that secures sustainable results. A part of your responsibility will also be to coach others to use and continuously improve the applied systems. When it comes to solving problems you will sometimes be responsible for driving the process and sometimes be supporting others in implementing and sustain defined solutions.

Besides leaders in your area you work closely together with a wide team of LEAN Partners, HR Partners and Training Partners within your assigned area. An outcome of this will be cross functional LEAN projects, defining and supporting improvement projects in your area and ensure on-boarding of new leaders in respect to the LEAN framework.

Qualifications
You hold a B.Sc., M.Sc. or similarly and through your studies and working experience you have gained a good understanding and have a great interest in being part of a process production setup. You can give examples of being part of; complex problem solving, systematic approach to problem solving, experience with applying different LEAN tools and experience that demonstrates a desire to drive change.

On a personal level, you have excellent communications skills both oral and written in Danish and English and show a natural interest in others. You are known as a fast learner with a desire to develop yourself and others and have a naturally strong personal drive and thrive driving your tasks independently. Are you talented and have the ambitions, taking up this job as Department LEAN Coordinator, might develop you into a future manager.

In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.

Contact
For further information, please call Nicolai Banck on + 45 3079 0484 or Marianne Baatrup Thystrup on + 45 3079 6662.

Deadline
4 May 2014.

Denmark - Hillerød Production
15-Apr-2014 Internship in Global Talent Attraction, Novo Nordisk
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Global Talent Attraction, Novo Nordisk

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Global Talent Attraction is part Corporate People and Organisation (Corporate HR) at Novo Nordisk A/S. Our main objective is to increase the knowledge and attractiveness of Novo Nordisk as a workplace across our key markets. We function as a centre of excellence for our business areas and help them address their specific challenges in attracting and recruiting new employees. You get the opportunity to join a team of 13 employees with a variety of backgrounds (HR, communication, marketing and international business). We use our differences to create novel ideas, attraction campaigns and high-quality solutions.

The job
We have a constant focus on optimising our activities and brand towards students in Denmark as well as globally, which is one of the areas you will be involved in during the internship. You will take part in various projects and tasks related to employer branding, workshop planning, working with social media, communication materials, benchmarking analysis, etc. The right candidate will have plenty of opportunities to influence the projects he/she will be involved in.

Qualifications
We are looking for an intern who is passionate about branding and communication. You are

currently studying on your master degree in communication, marketing, HR or related fields.

The ideal candidate has some experience with branding or event management. Some

knowledge of Photoshop and/or InDesign would also be an advantage.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 1 September 2014

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Caroline E. Bloch Poulsen-Hansen on + 45 3075 2347.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
15-Apr-2014 Internship in Biopharm Operations, Strategy & Sourcing
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Biopharm Operations, Strategy & Sourcing

  • Business Support
  • Denmark - Måløv

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Novo Nordisk is seeking an engaged student for full time internship to BRU Operations in a period of 4-6 months. BRU Operations is part of Biopharmaceuticals Research Unit (BRU) which develops new research projects within three therapeutic areas; haemophilia, growth hormone and inflammation. BRU is a global organisation with 600 employees split between Måløv, Seattle and Beijing

The job
You will be working in a dynamic team with 6 other dedicated employees in Måløv. The department’s main responsibility is to deliver high quality support to management through ensuring effectiveness and efficiency in business processes, management presentations, balance scorecard process, secure portfolio planning and prioritisation as well as participation in multiple projects optimisation projects.

During your internship you will be responsible for individual deliverables and will participate in larger cross functional projects. You will be given a unique opportunity to gain a broad insight to the business and key processes. You will get hands-on project management experience in a dynamic environment, working with a dedicated and ambitious team.

Qualifications
You are currently pursuing a Master’s degree in Finance, Business Administration, Engineering or another relevant degree, and have had excellent result during your studies. You pay attention to details and possess good communication skills. You like being part of a professional team, have a high energy level, take initiative (proactive thinking) and work with a high level of engagement. You are motivated by being challenged both professionally and personally. You have a flair for IT (Excel and Power Point) and numbers. We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. The atmosphere in BRU Operations is informal and humorous.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Practicalities

Qualification: Students in first or second year of master degree

Period: The internship position is a full-time position for 4-6 months.

Desired start date: 1 August 2014

Contact
For further information, please call Anders Mikkelsen on + 45 3079 4461.

Deadline
1 June 2014.

Denmark - Måløv Business Support
15-Apr-2014 QA Assistant
Do you want to work with Quality Assurance and secure quality mind set in a complete supply chain. Do you like cooperate with our internal stakeholders all over the world and secure timely approval of materials...

QA Assistant

  • Quality
  • Denmark - Bagsværd

Do you want to work with Quality Assurance and secure quality mind set in a complete supply chain. Do you like cooperate with our internal stakeholders all over the world and secure timely approval of materials? Then we have the right job for you in Sourcing QA.

About the department
Sourcing QA, Team Printed Packaging Materials is responsible for Quality Assurance of Printed Packaging Materials going into Novo Nordisk A/S Products. The team is responsible approval of Printed Packaging Materials for all Danish packaging sites, setting direction and approve specifications for Printed Packaging Materials worldwide. In the years to come we are facing challenges regarding global alignment between our NN production sites and standardisation of frame methods for quality control and batch releases. The team consist now of 3 QA assistants and 7 QA professionals.

The Job
You will work closely together with the 2 other QA assistants and be responsible for timely approval of Master data in SAP and MPO approval in PRISM, Review of batch documentation and disposition of printed packaging materials from our QC incoming control. Furthermore you will support the team in daily tasks such as updating relevant documents, review of NC and IC’s, data analysis and archiving GMP documentation. Challenges. We work in a dynamic and challenging environment with short deadlines, so you must be able to make prioritisations and take responsibility for customer requirements also when the solution is not obvious. You must be capable of working independently and support the team in the daily tasks. We have a high focus on launches and lead times in order to secure a high level of quality and compliance in the entire supply-chain from our suppliers to release of products.

Qualifications
Relevant technical or academic rank. You have a strong quality mind set and a good knowledge of GMP rules and quality assurance in the pharmaceutical industry. As we are cooperating broadly with many stakeholders (QC, Regulatory department, R&D) good collaboration and communication skills are needed. As a person you are known for your positive mind set and you enjoy working in a dynamic environment with many simultaneous tasks and changing priorities. You must be fluent in Danish and English, both written and spoken. We offer a very exciting job with excellent development opportunities among highly competent colleagues in a positive working environment.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Karin Løbel-Moberg on + 45 3075 8463.

Deadline
25 April 2014.

Denmark - Bagsværd Quality
15-Apr-2014 Training Development Consultant
Can you help Corporate Quality set the direction for future training? Do you have a proven record in developing targeted and worthwhile training that supports the business needs? Do you thrive in a busy, growin...

Training Development Consultant

  • Quality
  • Denmark - Bagsværd

Can you help Corporate Quality set the direction for future training?

Do you have a proven record in developing targeted and worthwhile training that supports the business needs?

Do you thrive in a busy, growing and global environment? ….then go for this job!

About the department
Quality Development is part of the Corporate Quality organisation in Novo Nordisk. We are a vibrant and experienced group of project managers, process experts and training development consultants all working to improve the Quality Management System. We are 26 dedicated employees organised in 3 departments: Quality Intelligence, Quality Projects and Quality Capability Development (QCD). The departments are located in Bagsværd, Denmark.

The Job
As a Training Development Consultant in QCD, your primary role is to set strategic direction and drive the development and roll-out of training tools, training metrics and training standards across Corporate Quality in close co-operation with rest of the training team.

You will support and inspire the internal trainers and subject matter experts to improve existing as well as develop new training activities by providing guidance and support regarding the pedagogical design and the selection of training methods and technologies.

You take responsibility for developing, managing and hosting extensive training programs such as our Quality Academy targeting QA professionals across Novo Nordisk and work closely with Project Managers e.g. as track lead striving to facilitate and develop world class training activities supporting the roll-out of Quality Projects globally.

Qualifications
You have an academic background such as HR, communication or science but more importantly you can demonstrate clear competencies in creating internal courses together with trainers and an ability to work both on a strategic and an operational level with relevant cross organisational stakeholders.

You are expected to have a good understanding of the full training process and can show evidence of having developed and delivered high quality training, training standards and training effectiveness measures in larger, global organisations.

Knowledge about Novo Nordisk or the challenge of organising training in a major pharmaceutical company and/or experience of project management would be an advantage.

You are an enthusiastic and committed person with the passion to drive improvements to training in quality processes from concept to implementation. You are service minded, independent and persistent.

We are determined to continually improve our work and it is therefore important that you are able to see and communicate opportunities instead of limitations and achieve results.

Contact
For additional information, please contact Mette Fjord Andersson on +45 3079 4692 or Sine Martinussen on +45 3075 9576.

Deadline
7 May 2014.

Denmark - Bagsværd Quality
14-Apr-2014 Regulatory Associate
Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk’s medicines approved across the globe. Our people have a unique combination of scientific insight and the abilit...

Regulatory Associate

  • Regulatory Affairs
  • Denmark - Søborg

Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk’s medicines approved across the globe. Our people have a unique combination of scientific insight and the ability to navigate many agendas and stakeholders. That makes Regulatory Affairs a truly interesting place to work – but also quite challenging. Are you up for the challenge?

We are currently looking for a Regulatory Associate with an interest in working with Life Cycle Management (LCM) activities to join our Modern & Human Insulins’ team. The vacant temporary position is of 12 months duration.

About the department
The Modern & Human Insulins’ team is a part of the Regulatory Insulins and Oral proteins department. In the team, we are 10 regulatory associates and professionals working with all the clinical regulatory LCM activities for our marketed modern and human insulin products.

The job
You will be substituting one of our regulatory associates, and your primary task will be to handle the administrative tasks needed for clinical LCM of one of our modern insulin products in close collaboration with the product responsible regulatory professional, internal stakeholders and affiliates worldwide. You will be administrative responsible for preparing, compiling and submitting documentation to health authorities, and assisting in ensuring approvals. You will also be handling requests from affiliates and other stakeholders. You will work in a fast paced environment with tight deadlines, and you will be supported by a team of friendly colleagues with a good sense of humour.

Qualifications
Preferably, you have experience from working in Regulatory Affairs. You have an educational background as pharmaeconomist, medical secretary, bachelor in science, marketing, English or similar. You have a flair for IT systems and experience with MS Office applications as you will be responsible for managing data entry and electronic filing in our various databases and document management systems. Fluency in written and spoken English is a must.

On a personal level, you are very structured, systematic and you have a strong quality mind-set. You are a team player, but also enjoy working independently. You have a positive attitude, good sense of humour, and you keep your spirits high also under pressure.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please call Dorte Tingskov on + 45 3075 8086.

Deadline
28 April 2014.

Denmark - Søborg Regulatory Affairs
14-Apr-2014 QA Professional
Biopharm New Haemophilia API QA is looking for a talented and ambitious QA Chemist Are you ready to assure quality and develop quality mindset in Novo Nordisk Product Supply? Then we have the job for you in Bio...

QA Professional

  • Quality
  • Denmark - Hillerød

Biopharm New Haemophilia API QA is looking for a talented and ambitious QA Chemist

Are you ready to assure quality and develop quality mindset in Novo Nordisk Product Supply? Then we have the job for you in Biopharmaceuticals Quality Assurance.

About the department
Biopharm New Haemophilia API QA is a dynamic department who are responsible for the quality assurance of our new haemophilia products. In this position you will have opportunities to learn about development and production of new products for the market and also get a solid understanding of manufacturing processes.

You will become part of a team which have a high level of self-governance. The team is responsible for the quality assurance for the cultivation and purification processes, equipment and facilities in API departments in Hillerød. The job includes QA review of several types of documents related to processes, facilities and equipment. The working relations are informal and the team value professional sparring and good humour highly.

The job
As a QA professional you will be responsible for ensuring that our products are manufactured according to our marketing authorisations. In our team we handle all kind of documentation on quality matters in the API department. This includes batch documentation, deviations, validation and changes in the production. Furthermore you will participate as an expert in relevant audits and inspections. You will continuously focus on ensuring a high compliance level in the supply chain. In a dynamic and challenging environment with short deadlines you are able to make clear prioritisations and take responsibility for customer requirements in many situations, including those where the solution is not obvious.

The position offers you a unique opportunity to leave your mark on the department, great potential for personal development while realising your goals and seeing the benefits of your work. When you start you will undergo an individual and intense training program.

Qualifications
You hold a Master’s degree or equivalent in pharmaceutical sciences, engineering or a related discipline. You have a strong quality mind-set and knowledge of GMP rules and preferable you have experience with production and/or quality assurance within the pharmaceutical industry. As we are cooperating broadly with many stakeholders, excellent collaboration and communication skills are needed.

Your language skills cover proficiency in both Danish and English. You work independently and make decisions regarding quality tasks and ensure the right balance between quality demands, authority demands and business needs. At the same time, you perform well in a team-oriented environment. As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments.

Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Ditte Kivsmose Kaldor on + 45 3075 7767 or Lars Nyholm on + 45 3075 5226.

Deadline
28 April 2014.

Denmark - Hillerød Quality
14-Apr-2014 Ambitious Medical Doctors with a global mindset
Join Novo Nordisk’s Pharmaceutical Medicine Programme! We’re seeking five MDs with a desire to explore career opportunities for MDs at Novo Nordisk. We don’t treat one. We treat millions...

Ambitious Medical Doctors with a global mindset

  • MD position
  • Denmark - Søborg

Join Novo Nordisk’s Pharmaceutical Medicine Programme! We’re seeking five MDs with a desire to explore career opportunities for MDs at Novo Nordisk.

We don’t treat one. We treat millions
Are you a medical doctor looking for a challenging career path in a pharmaceutical company? Would you like to be part of highly qualified and ambitious teams in a global setting? Then this is your unique opportunity to apply for a position with three job rotations where you can use your medical and scientific knowledge in an inspiring way to create better treatments and care for our patients.

Novo Nordisk is seeking ambitious medical doctors, who are interested in getting an insight into the pharmaceutical industry and have the ambition to impact lives of millions of people with diabetes and other therapy areas covered by Novo Nordisk. Our Pharmaceutical Medicine Programme is a permanent position in Novo Nordisk where the first two years are fixed in a rotation between three key departments. This position offers you the opportunity to build a life changing career with possibilities for personal and professional development, as well as a chance to work alongside the best in the field.

“I have experienced that Novo Nordisk offers me the opportunity to work with highly qualified colleagues in an informal and engaging atmosphere” (Signe Diness Vindeløv, Global Medical Affairs)

Take your career to a new level
The Pharmaceutical Medicine Programme offers you employment on regular permanent terms, starting with a two year learning journey, where you will work with three core elements of pharmaceutical industry – drug development, drug safety and medical affairs – and thus be introduced to a variety of different assignments requiring medical and scientific expertise. We offer an inspiring and ambitious working environment with a mutually rewarding commitment, alongside the flexibility that allows you to shape your own working day.

All rotations will take place at our corporate headquarter in Denmark. However, some travelling is expected. After successful completion of the two-year programme you will be offered a regular medical position in Novo Nordisk.

“It is actually very often that I seem to forget I’m working for a company that creates revenue. My focus is always on the patients need first and thereby working for Novo Nordisk doesn’t differentiate from my previous work in the clinic” (Anne Birk Østerskov, 3rd rotation, Global Development)

MD with two-five years of research and/or clinical experience
In order to qualify for the position you must hold a university degree as a Medical Doctor. You should not have previous experience within pharmaceutical industry. You must have passed post-graduate internship, have two-five years of clinical experience and preferably documented research. You must have practical and analytical skills and be capable of working in a culture of respect, teamwork and personal responsibility.

It is expected that you contribute with your own ideas as well as build upon the ideas of others. Moreover, you should be willing to travel and work in an international arena. We expect that you are fluent in written and spoken English and have a high proficiency in IT knowledge.

”The PMP programme gives you a great opportunity to practice both your scientific and personal skills in a variety of settings. Working closely with skilled people with different backgrounds and mind-sets are very inspiring and makes you learn a lot on many different levels” (Frida Emauelsson, 1st rotation, Global development)

Meet MDs at the career website
Meet both former and current MD’s and read more about the programme at novonordisk.com/PMP. Feel free to share these job opportunities by using below functionality.

Contact
For further information, please contact Programme Responsible Anne Kaas

Deadline
4 May 2014

Denmark - Søborg Research & Development, Medical Doctor
14-Apr-2014 Senior Scientist
Are you interested in the in vitro pharmacology of incretin-based therapies? Are you ready to help us find new GLP-1 analogues? ...

Senior Scientist

  • Research & Development
  • Denmark - Måløv

Are you interested in the in vitro pharmacology of incretin-based therapies? Are you ready to help us find new GLP-1 analogues?

About the department
The Receptor Pharmacology team is part of the Incretin and Islet Biology department and based in the Diabetes Research Unit. The team focuses on in vitro pharmacology and biology related to our incretin-based therapy research. Receptor Pharmacology consists of 5 scientists, 8 technicians and 6 students that have responsibility for the following: screening of new analogues, development of new assays with emphasis on incretins and GPCRs, mode of action support for discovery projects, introduction of new assay technologies and support of basic research in the biology of incretin hormones

The job
Your focus will be to deliver in vitro functional and receptor binding assay results as a part of our screening program. You will also be responsible for performing mode of action studies in recombinant and natural cell systems. You will work in project teams with scientists from other areas of diabetes research and in that role will be expected to communicate your results effectively in technical reports and oral presentations.

You will be expected to keep abreast of new developments in the fields of incretin hormones and GPCR receptor pharmacology. You will also participate in international scientific conferences and collaborations.

Qualifications
You have a PhD or similar degree/experience in the biological sciences and your professional career has had a focus on receptor pharmacology. You have extensive experience in setting up cell-based assays with a focus on GPCRs. You are familiar with state-of-the-art techniques and computational tools in the field and can contribute significantly to the team in these areas. Knowledge of incretin pharmacology is preferable but not a must. You are fluent in English and understand how to succeed in an international environment.

We offer an exciting job with lots of challenges among good colleagues in a positive working environment.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information about the job please contact Jim McGuire +45 3079 6122 or Sanne Møller Knudsen +45 3075 4555.

Deadline
30 April 2014.

Denmark - Måløv Research & Development
14-Apr-2014 Senior Project Manager for hGH
Want to work with BioPharm's broad product portfolio and help us to become fast to Market? In Biopharm Manufacturing Development, we are responsible for support to our productions, the transfer of new products ...

Senior Project Manager for hGH

  • Project Management
  • Denmark - Gentofte

Want to work with BioPharm's broad product portfolio and help us to become fast to Market? In Biopharm Manufacturing Development, we are responsible for support to our productions, the transfer of new products from R & D and ongoing optimization of our many processes.

About the department
You will be part of Biopharm Project Office within our Manufacturing Development function. Main responsibilities for the Biopharm Project Office is project management of CMC-activities on marketed products; CMC coordination of life cycle management projects; execution of process improvement projects and portfolio management of Biopharm MDev projects.

The Job
As senior project manager for the Growth Hormone project portfolio you will be responsible for driving optimization projects on our marketed products and production processes and thus help to ensure that Biopharm consistently delivers optimally and achieve its strategic objectives. You will be CMC coordinator in the Lifecycle Management core team and be responsible for product optimization within the team.

Qualifications
You currently work as a project manager or line manager and has completed your academic background as a Master in engineering, pharmacy, MSc. with several years of experience in pharmaceutical production, manufacturing development, quality and lean manufacturing. Through your work, you have gained experience with the transfer of products and ensured a good insight into the production of finished goods. You thus have an understanding of the process from the cell bank to packaged product and the applicable regulatory matters. With your optimistic and flexible approach to your challenges you are able to navigate in a changing environment and take pride in completing complex projects in organizational contexts with many different stakeholders, scarce resources and high management attention. You are able to view and analyze complex issues and illustrate possible scenarios. You are convincing in your communications and ability to find the way forward. As a facilitator, you achieve consensus in relation to the direction and approach and ensure a clear structure and plan for your work. You speak and write English.

At Novo Nordisk, we work together to prevent, treat and eventually cure diabetes. Nearly 366 million people worldwide are living with diabetes today, with two people diagnosed every ten seconds. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Henrik Melgaard at + 45 3075 7757.

Deadline
30 April 2014.

Denmark - Gentofte Project Management
14-Apr-2014 Sr. Research Scientist
You now have the opportunity to play a key role in developing formulations and freeze drying processes for the next generation of biopharmaceuticals. A challenging job for an experienced scientist is available ...

Sr. Research Scientist

  • Research & Development
  • Denmark - Gentofte

You now have the opportunity to play a key role in developing formulations and freeze drying processes for the next generation of biopharmaceuticals. A challenging job for an experienced scientist is available in team Biopharm Formulation Development I, a team responsible for development of biopharmaceuticals - all the way from early development to phase III clinical trials and registration.

About the department
Biopharm Formulation Development is part of Injectable Protein Formulation in the R&D area CMC Supply. As the link between research unit and production we are responsible for developing formulations and production processes for primarily freeze dried and soluble injectables of new haemostasis and inflammation products. Due to our rapidly increasing project portfolio, we are now facing new exiting challenges. Team Biopharm Formulation Development I is located in Gentofte (Copenhagen, Denmark), and consists of 6 Technicians, 7 Scientists/Specialists and one Team Leader.

The job
We offer you a position, where you will have responsibility for development of formulations and freeze drying processes assuring optimal biopharmaceutical characteristics. The development projects will be within haemophilia products, monoclonal antibodies and growth hormones. Your daily work will be in close collaboration with a project team and you will design, interpret and report studies on drug product and freeze drying processes - hereby generating pharmaceutical documentation for internal and external use. You will interact with a wide variety of internal stakeholders, e.g. Production (Product Supply), Regulatory affairs, Quality Assurance, Analytical Development, Production Pilot Plant and Discovery.

Qualifications
You hold a Master of Science possibly combined with a PhD in Chemical Engineering, Pharmacy or another relevant scientific discipline. You have working experience within drug product development. Candidates with knowledge and experience with freeze drying processes of therapeutic proteins will be preferred. As a person you are result-oriented and flexible. You enjoy working in a team with highly motivated people, dedicated to developing the next generation of biopharmaceuticals. You work systematically, have good collaborative skills and have knowledge of strict documentation standards. You possess drive and a positive mindset, and you strive to make the best scientific solutions.

At Novo Nordisk we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous scientific challenges.

Contact
For further information, please call Charlotte Rossmeisl on + 45 3075 4035.

Deadline
28 April 2014.

Denmark - Gentofte Research & Development
14-Apr-2014 Quality Coordinator in Supply Chain Planning
Are you passionate about maintaining and improving quality and compliance? Are your keen on working internationally and have an interest in Supply Chain Management? Then, we may have the right position for you....

Quality Coordinator in Supply Chain Planning

  • Supply Chain and Logistics
  • Denmark - Bagsværd

Are you passionate about maintaining and improving quality and compliance? Are your keen on working internationally and have an interest in Supply Chain Management? Then, we may have the right position for you. As Quality Coordinator, in Shipping and Customer Service, a department within Supply Chain Planning, you will play a key role in ensuring that the department constantly meets the regulatory requirements within ISO and GMP. You will become part of a dynamic work environment with direct access to our global customers.

About the department
You will be a part of the Shipping & Customer Service department, which handles shipping of finished products and raw materials. 37 dedicated colleagues ensure fast and reliable global import/export of Novo Nordisk’s products to our affiliates and direct customers around the world in the right quality and at competitive prices.

The job
As Quality Coordinator, you are quality responsible for the department and support and guide the unit in quality related issues. This includes acting as unit GxP training coordinator as well as unit review coordinator and handling the change requests and

non-conformities relating to transport.

Additionally, you are responsible for transport process validation, e.g. ensuring quality and compliance when transporting Novo Nordisk’s products. In particular, it is your responsibility to make protocols and document that the products stay within the specific standards of tolerance from the moment they leave the ramp at Novo Nordisk until they reach the final destination somewhere in the world. You play a key role in preparing and presenting validation documents for Danish and international authorities, and you participate in the audits and inspections, giving a detailed account of the validation methods and the results.

Furthermore, you will contribute to managing the daily use and maintenance of the IT system used for temperature monitoring during transport and for validation in connection with upgrade and changes to the system.

You can look forward to a global and independent job, where you will be in contact with stakeholders from all over the world and play a major role in our efforts to live up to all QA and QC requests.

Qualifications
You have a Msc in Engineering, Pharmacy or similar, combined with experience from a similar position or a position within QA or QC. It is an advantage if you also have experience with process validation. In everything you do, you are driven by your strong personal commitment and sense of responsibility and you are not afraid to stand your ground when needed. You have a systematic and thorough approach to your work and you are keen on finding sustainable solutions. You have a sense of initiative and enjoy an independent role where you work as the go-to-person who possesses solid in-depth expertise within your field of work. This job also requires excellent communication and cooperation skills, as you navigate your way around colleagues, foreign authorities and other stakeholders, and balance support and continuous follow-up. Finally, you take pride in meeting your deadlines and you never compromise on quality in your work.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Christina Grauballe on + 45 3075 2053.

Deadline
30 April 2014.

Denmark - Bagsværd Supply Chain and Logistics
14-Apr-2014 Internship in FLIR Executive Office – Quality
Novo Nordisk is one of the world’s most successful pharmaceutical companies. At Novo Nordisk we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join ...

Internship in FLIR Executive Office – Quality

  • Student and Internships
  • Denmark - Bagsværd

Novo Nordisk is one of the world’s most successful pharmaceutical companies. At Novo Nordisk we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort.

Novo Nordisk is seeking an intern in FLIR Executive Office in Bagsværd from 11 August 2014 to support our efforts in supporting management decisions and managing our Quality function.

About the department
FLIR Executive Office consists of a management support unit and an internal consultancy - both supporting our CFO in facilitating decisions and driving key projects throughout Novo Nordisk’s global organisation.

Together with FLIR Consulting, FLIR Executive Office makes up a young, diverse department consisting of 12 dedicated employees with backgrounds from top-tier consultancies or with previous Novo Nordisk experience.

The job
As an intern in FLIR Executive Office, you will drive management support and quality management processes. Your areas of responsibility include reporting on quality improvements, assessing and implementing new internal requirements, reviewing compliance levels, and generally supporting the quality function through projects and ad-hoc tasks.

You will be working closely together with the department Quality Manager and you will be exposed to senior stakeholders. You will get hands-on experience with Novo Nordisk's quality management system, as well as best practice project management methods and tools.

Qualifications
You are a master’s degree student in Business Administration, Supply Chain Management, Engineering or similar in the first or second year of your studies. You take an interest in project work, as well as process, quality and project management.

You are among the best in your class, fluent in English and are used to working independently as well as in teams. You approach tasks in a structured way with a good sense for detail. Finally you have a positive attitude.

Your development is important to us. Training and personal development are key tools to ensure continuing development of your toolbox.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Practicalities:

Period: The internship position is a full-time position for 5-6 months

Start date: 11 August 2014

Contact
For further questions, please call Nina Correll on + 45 3075 5009.

Deadline
10 May 2014.

Denmark - Bagsværd Student and Internships
12-Apr-2014 Finance intern
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Finance intern

  • Student and Internships
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will be part of a small dynamic team developing and driving Financial Management in DMS, who has global responsibility of delivering plastic components for Novo Nordisk injection pens. We value professionalism and responsibility, and have an open and informal team culture. We ensure an environment, where we focus on continuously improving individual and team competences. You will interact in teamwork with your colleagues, and have a broad list of contacts throughout the organization.

The job
You will be involved in a broad variety of activities related to Management Accounting, fx. Month end closure and Management reporting and Controlling. You will assist the team in performing follow-up on Financial Performance through daily and weekly deliverables to internal and external stakeholders on Operating Cost and Investments. Furthermore, you will solve day to day Accounting issues. As an Intern, you will get insights on how to operate a Finance function in an efficient and value adding way.

Qualifications
You want to use your solid financial knowledge and get energy from delivering results and continuously improving existing processes. You are currently studying on your master’s degree in Finance or Economics (Cand.Merc, Cand. Polit or similar). You have a solid understanding of Management Accounting and Reporting. You like working with numbers, have excellent analytical skills and you are an Excel super-user. You have fluency in both oral and written English, sound personal judgment and excellent interpersonal skills. You work in a structured way and have a sharp eye for details. You can handle many tasks simultaneously, have a strong focus on quality and wants to deliver results. As a person you are ambitious, dedicated, and you can easily interact with employees at all levels in the organization.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 1 August 2014

Contact
For further information, please contact Anders Hvidt on +45 3075 4023.

Deadline
2 June 2014.

Denmark - Hillerød Student and Internships
12-Apr-2014 Internship in Sourcing Operations Business Support, Novo Nordisk
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Sourcing Operations Business Support, Novo Nordisk

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will join an exciting and ambitious supply chain organization in Bagsværd. We are responsible for the inbound supply of materials to NNs production sites world-wide. We source materials, store them, perform quality control and supply them to the production sites. We strive for running an increasingly integrated and seamless supply chain, which is what we need the right intern to support us in.

The job
You will play a key role in mapping and optimizing the flows and value stream across Sourcing Operations. You will support our Project Managers in performing Value Stream Mapping across our value chain and within specific processes. Furthermore you will based on your specific interests and competencies – be involved in concrete LEAN improvement initiatives. Your job will be a combination of teamwork and individual contributions, and you will on a daily basis interact with many different kinds of people. If you are eager to learn, engaged and takes responsibility you will experience a trusting support to your development.

Qualifications
We imagine that your master studies is somehow related to supply chain. Whether with a technical, business or natural science angle is of less importance. We expect that you are able to rapidly navigate in a complex and somewhat ambiguous environment, and thus preferably have experience with working in a larger organization. You have knowledge of and preferable experience with LEAN tools and practices. Personally you are motivated by making a difference to other people, and prefer to act in order to learn. You are fluent in building relationships and interact confidence inspiring with other people. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Our business language is English, however in order to be able to work effectively on the shop floor, you need to have strong oral Danish skills as well.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 25-08-2014

Contact
For further information, please contact Mads Yding Lind on +45 3079 8103

Deadline
02 June 2014.

Denmark - Bagsværd Student and Internships
12-Apr-2014 Internship with focus on LEAN improvement, Novo Nordisk
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship with focus on LEAN improvement, Novo Nordisk

Learn more about the largest site in Novo Nordisk's global production network using this link www.novonordisk.com/kalundborg-careers

  • Student and Internships
  • Denmark - Kalundborg

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will join our new Multiline Purification Department. We are part of Insulin Manufacturing 1 with a total of 390 people in Kalundborg. You will also be part of our very strong LEAN team where cooperation and unity are key words. Novo Nordisk in Kalundborg is a city within the city. The area is situated a good hour from Copenhagen and covers 1,350,000 m2, including a private roadgrid. We produce some 50 % of the insulin in the world and w you are pursuing a master’s degree e are at the front edge of the development within technology, systems, methods and processes.

The job
Your focus is to continuously improve LEAN competencies and to support activities in order to improve stability and quality from fermentation/recovery to purification. Everybody – Managers as employees – must be equipped with the right tools that enable them to work with a very high quality mindset and as efficiently and as cost-consciously as possible. You will therefore spend a lot of your time in the production area where you spot processes and methods with LEAN improvement potential – data crunching is another part of this. You see, you solve, you share and follow-up on problems. As part of the job you support managers across the entire facility in the development of LEAN systems and methods, e.g. performance boards, problem solving and process confirmation. Standardisation, alignment and best practice sharing will be the key to your success.

Qualifications
We are looking for an intern who is passionate about LEAN, production processes and uptimization. You are currently pursuing a master’s degree in pharmacy, public health, health services research, health economics/economics or other relevant field.

We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. Ability to manage a large volume of projects (with supervision); sound personal judgment; and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

In combination with your natural interest in others and your ability to put yourself in charge you master the fine art of knowing when to compromise and when to stand firm. You are able to independently plan and drive your own tasks. If you do not already master Excel, you demonstrate your fast learning capabilities here as well.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Practicalities

Requirement: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01-08-2014

Contact
For further information, please contact Ronnie Hansen +45 3079 2995

Deadline
02 June 2014.

Denmark - Kalundborg Student and Internships
12-Apr-2014 Internship
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship

  • Student and Internships
  • Denmark - Bagsværd

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring energy and new ways of thinking to our company.

About the department
Site Denmark Data Management is seeking an engaged student for a salaried full-time internship for a period of 6 months commencing June 2014. Site Denmark (SDK) is the Danish site in Diabetes Finished Products where insulin is filled, assembled and packed within Novo Nordisk. SDK is the largest producer of finished insulin products in Novo Nordisk.

The SDK Data Management team is a newly created team dedicated to support the performance management of Site Denmark, and this particular internship takes place in Bagsværd.

The job
You will be working in young and dynamic team with four dedicated employees. Among other things we are responsible for driving the performance management across Site Denmark. During your internship you will be responsible for improving the data and visual structure of our KPIs as well as driving problem solving in ad-hoc projects. Furthermore you will be responsible for an improvement project to be defined in collaboration with your manager, which can link to your study programme.

Qualifications
You like working with numbers, have excellent analytical skills, you are an Excel super-user and have experience in programming. You are studying for a degree in Business, Engineering, Supply Chain Management or any other relevant degree. Only candidates who have not yet finalized their degree will be considered for the internship.

As a person you are ambitious, dedicated and a team-player. You have good communication skills and can easily interact with employees at all levels in the organization. Your tasks will require independence, a flexible approach and good oral and written communication skills.

You have solid interest in Data Analysis and but also curious about Supply Chain, and you can see yourself working in Novo Nordisk in the long run.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Stephane Chong on +45 3075 1072.

Deadline
2 June 2014.

Denmark - Bagsværd Student and Internships
12-Apr-2014 Internship in Process Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in Process Support

  • Production
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
You will be a part of a dynamic and high performing Process Support team in Hillerød, responsible for supporting the production of plastic components for Novo Nordisk medical devices. We value professionalism and responsibility, and have an open and informal team culture. We ensure an environment, where we focus on continuously improving individual and team competences. You will interact in teamwork with colleagues, and have a broad list of contacts throughout the organization.

The job
You will be involved in a broad variety of activities related to Process Support in day-to-day business processes and tasks.

You will assist the team in performing follow-up on Process Support performance through daily and weekly deliverables to internal and external stakeholders. As Intern, you will get insights on how to operate in Process Support in an efficient and value adding way.

Qualifications
We are looking for an Intern who is passionate about delivering results and continuously improving existing processes.

You are currently studying on your master’s degree in engineering or Cand.Merc or similar. Fluency in both oral and written English; ability to manage a large volume of projects (with supervision); sound personal judgment; and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 4-6 months.

Start date: 01-08-2014

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Thomas Iversen on +45 3075 6219.

Deadline
2 June 2014.

Denmark - Hillerød Production
12-Apr-2014 Intern with ambition and focus on production planning
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Intern with ambition and focus on production planning

  • Student and Internships
  • Denmark - Hillerød

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring energy and new ways of thinking to our company.

About the department
Product Supply in Novo Nordisk is seeking an engaged student for a salaried full-time internship in Site Denmark Logistics in a period of 6 months commencing August 2013. Product Supply is an organization with close to 10,000 employees located in Denmark or at one of our five international production sites. Product Supply is responsible for all production in Novo Nordisk and delivery of products to our sales affiliates or directly to major customers. Site Denmark is one of these five productions sites located in Kalundborg, Bagsværd and Hillerød, and this particular internship takes place in Hillerød.

The job
You will be working in a challenging and highly dynamic logistics team with ten dedicated employees. Among other things we are responsible for planning a production running 24/7, which requires a combination of excellent planning and fast containment of problems. During your internship you will be responsible for a number of operational tasks within FlexPen® assembly and pack including production planning in close collaboration with the production, handling raw materials & packaging materials, updating logistic KPI’s and driving problem solving. Furthermore you will be responsible for an improvement project to be defined in collaboration with your manager, which can link to your study programme.

Qualifications
You are studying for a degree in Production Engineering, Logistics, Supply Chain management or any other relevant degree. Only candidates who have not yet finalized their degree will be considered for the internship.

Besides this, personality is the key word. You are positive, independent, energetic and flexible. You see solutions instead of problems and you take initiative to implement these solutions. You get the job done.

You have solid interest in Production and Logistics, and you can see yourself working in Novo Nordisk in the long run.

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please call Carl Johan af Rosenborg on + 45 3075 6719.

Deadline
2 June 2014.

Denmark - Hillerød Student and Internships
11-Apr-2014 Director
Are you on the lookout for the opportunity to combine your scientific understanding, regulatory insight, and leadership skills? ...

Director

  • Management
  • Denmark - Søborg

Are you on the lookout for the opportunity to combine your scientific understanding, regulatory insight, and leadership skills?

About the department
At Novo Nordisk Regulatory Affairs (RA), we strive to make new and better medicines available worldwide, for among others people with diabetes and haemophilia. In the haemophilia area we currently have 2 new haemophilia drugs in phase 3 development and 1 drug under review by the regulatory authorities.

The job
As Department Director your primary focus is to manage the growing Factor VIII and Factor IX projects department which has one drug under review and two which will soon be submitted for regulatory approval. Our organisation is dynamic, with change management being an integral part of our everyday life. The job puts high demands on your leadership skills in terms of performance management and your ability to develop a staff of 15+ direct reports on the basis of individual and business needs.

You secure the quality of the documentation submitted to health authorities, and in this respect will be supported by Regulatory Project Managers, professionals, and associates in our organisation.

You report to the Corporate Vice President, RA Haemophilia and are a member of the Area’s line management team that is responsible for organisational and staff matters, including the optimising of resources across the Area. You will also be member of the wider Project management team together with our US based colleagues driving the regulatory progress of our portfolio in the US. In addition, you will be involved in cross functional projects and improvement initiatives within and outside the RA organisation, as well as collaboration with medical/clinical, marketing, product supply and quality assurance departments.

Qualifications
We expect you to have a university degree in science and a proven record of extensive global regulatory understanding and experience, successful liaison with regulatory authorities, profound understanding of haemophilia or other rare diseases, as well as cross-organisational experience in global drug development.

You have documented leadership experience: you set direction, lead and motivate your staff to work for joint objectives.

As a person you are well organised and have solid problem-solving capabilities, just as you show a winning attitude and never lose your strategic focus. You can keep your spirits high even when under pressure, and as a skilled communicator you can cooperate at any organisational level. Finally, you are comfortable using your fluent written and spoken English on a daily basis.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Henrik K. Nielsen on + 45 3079 6298 or Lene G. Sommer on + 45 3075 9762

Deadline
28 April 2014.

Denmark - Søborg Management
11-Apr-2014 Regulatory Associate
Are you the new Regulatory Associate for Victoza? If so, you may be the associate we are looking for. ...

Regulatory Associate

  • Administrative
  • Denmark - Søborg

Are you the new Regulatory Associate for Victoza? If so, you may be the associate we are looking for.

About the department
We are a department of 11 people working with marketed Victoza that is one of our block-buster products that is used for treatment of people with type 2 diabetes. We are looking for a Regulatory Associate to join our team working mainly with the centralised procedure in the EU and with national product licenses worldwide.

The job
In close collaboration with a team of other associates, experienced professionals, and regulatory project managers you will be responsible for our administrative processes in an environment with a high pace, many different tasks and short deadlines.

You will administer and coordinate a wide range of regulatory tasks to ensure a smooth workflow in our department – but also among our stakeholders within Novo Nordisk headquarters and affiliates. Your focus will be working with clinical documents in relation to variations, renewals and new registrations. In collaboration with the team you will ensure planning as well as timely submissions of high quality applications to Health Authorities worldwide. You will ensure adherence to important internal working processes such as workflow for variation submissions world-wide as well as adherence to the many complex processes with EU centralised procedure submissions such as grouping and work-sharing.

Qualifications
You have a relevant background as a pharmaconomist, medical secretary, librarian, bachelor in science, or similar from the pharmaceutical industry. Using IT such as electronic document management systems and the Microsoft Office package professionally comes naturally to you. You are a team-player, have a positive mind-set and a good sense of humour. Flexibility, managing tight deadlines and a sense of details are your strongest assets as well as a strong quality mind-set. Fluency in written and spoken English is a must.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Director Lene Melchiorsen at + 45 3079 1993.

Deadline
2 May 2014.

Denmark - Søborg Administrative
11-Apr-2014 CCGloW Expert
This is a highly versatile job where you will gain broad exposure to the company through interaction with stakeholders in R&D, Global Development and Product Supply along with our affiliates around the glob...

CCGloW Expert

  • Quality
  • Denmark - Bagsværd

This is a highly versatile job where you will gain broad exposure to the company through interaction with stakeholders in R&D, Global Development and Product Supply along with our affiliates around the globe. It requires deep process understanding, database super-user skills and excellent communication.

About the department
CCC is responsible for handling and evaluating product complaints from around the world. We work at the interface of our products and patients, and are responsible for maximizing the value of patient feedback by capturing and incorporating it back into Novo Nordisk processes. We are a part of Global Safety, located in the House of Quality in Bagsværd.

The job
The job is a permanent position and starts asap - latest 1st of July 2014.

Your main tasks are to ensure development of system improvements, and to provide tools for reporting (views) via high level SQL development tasks. This includes idea collection, specification, prioritization, testing and implementation.

You are also the bridge between users and various internal & external IT organizations. This requires excellent communication skills including the ability to translate the specialized processes & language of complaint handlers into the technical language of IT supporters & developers.

Together with colleagues, you will also be responsible for providing functional support to our 600+ users worldwide - primarily through our superuser network. This involves direct user training, coordination of our annual conference and process development.

Our users comprise production sites, R&D, and several of our international affiliates, hence in addition to bridging with IT units, you will also work broadly within Novo Nordisk.

Qualifications
You hold an academic degree in IT, engineering, mathematics, pharmaceutical sciences, or a related natural science discipline. The ideal candidate also has experience working with complaints in a production environment and programming in high level SQL.

You grasp complex processes, quickly gaining an overview while maintaining attention to detail. You communicate well – in spoken and written English - with non-technical users and IT technicians alike. In general, you are IT savvy, and work in a structured manner with a high quality mindset. You are a completer, but also flexible to changing priorities, You are a positive and open minded team player.

We offer a very exciting job amongst good colleagues with diverse backgrounds in a positive, dynamic working environment.

At Novo Nordisk, decisions and actions are based on their impact on society, the environment and on their potential to generate a profit. That makes for a responsible culture with a healthy and engaging working environment.

Contact
For further information, please call Julie Gillin on + 45 3075 6065.

Deadline
2 May 2014.

Denmark - Bagsværd Quality
10-Apr-2014 GMP Coordinator
Are you interested in working with our broad portfolio of products in Biopharm and help us with our delivery and Quality? In Biopharm Manufacturing Development we are responsible for support to our productions,...

GMP Coordinator

  • Production
  • Denmark - Gentofte

Are you interested in working with our broad portfolio of products in Biopharm and help us with our delivery and Quality? In Biopharm Manufacturing Development we are responsible for support to our productions, transfer of new products from R&D and continuous optimizations of our many processes. You will be a key player in ensuring quality and compliance for Biopharm AP Support consisting of a number of teams. You will be a member of the local Management team and primary sparring partner for the Director and Associate Managers on GMP issues.

About the department
We focus on support to Bioparm AP production, product transfer from R&D and stability of our products. You will have more than 50 highly qualified and motivated colleagues. You will be responsible for GMP and Quality and refer directly to the Director for Biopharm AP Support.

The job
As GMP Coordinator you have the overall responsibility for setting the targets on quality and compliance for your area and for making sure that they will be met. As such, you bring in the latest knowledge within GMP when you challenge our business managers to bring GMP and quality to the top of the agenda. You ensure that the area is in compliance with the authorities’ and Novo Nordisk’s regulations, including ISO9001:2008, and you will become your area’s representative in our cross-organisational GMP group/GMP board. You are also responsible for the departments input to the Quality Management Review (QMR), and you play an active role in audits and inspections. You will participate in our GMP network meetings with your peers for sparring, sharing and development of GMP and QMS related topics. Furthermore, part of the job will be to assist, in the beginning, our Stability team with various tasks and later on other tasks across the department.

The job involves contact and interaction to many different stakeholders in the organisation, from operators, maintenance, LEAN professionals, project managers, and to all line management levels.

Qualifications
You hold a degree at minimum master’s level. Your academic background is topped with experience from a pharmaceutical production company where you have gained solid experience within quality, GMP and ISO9001. You are used to create results through projects and know the importance of team collaboration. To succeed, you must thrive in a role where you take leadership, initiate and coordinate a large number of actions and projects. This requires an excellent overview, a structured mind-set and a dedicated way of working as well as very good communication skills. Working cross-organisationally, your networking skills will also be crucial as well as your ability to balance when to compromise and when to stand firm. Finally, you must master English and Danish, written and spoken.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please call Martin Arendt Petersen on + 45 3079 8228.

Deadline
26 April 2014.

Denmark - Gentofte Production
09-Apr-2014 Internship in CMC DP Business Support
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship in CMC DP Business Support

  • Business Support
  • Denmark - Måløv

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

About the department
Novo Nordisk is seeking an engaged student for full time internship to CMC Drug Product (DP) Development Business Support in a period of 6 months. CMC DP Development is part of CMC Supply, which manufacture and distribute drug candidates for pre- and clinical trials, develop commercial manufacturing processes and technologies and produce scientific documentation. CMC DP Development is an organisation with app. 400 employees located in Denmark.

The job
You will be working in a dynamic Business Support team with 8 other dedicated employees in Måløv. The department’s main responsibility is to deliver high quality support to management through ensuring effectiveness and efficiency in business processes, management presentations, performance measurement, balance scorecard process as well as participation in multiple projects.

During your internship your key task will be to deliver high quality support to the team. You will be involved in securing high quality in the monthly performance follow-up as well as participate in cross functional projects. You will be given a unique opportunity to gain a broad insight to the business and key processes. You will get hands-on project management experience in a dynamic environment, working with a dedicated and ambitious team.

Qualifications
You are currently pursuing a Master’s degree in Finance, Business Administration, Engineering or another relevant degree, and have had excellent result during your studies. You pay attention to details and possess good communication skills. Excellent language skills in English and Danish are required.

You like being part of a professional team, have a high energy level, take initiative (proactive thinking) and work with a high level of engagement. You are motivated by being challenged both professionally and personally. You have a flair for IT (Excel and Power Point) and numbers. We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. The atmosphere is informal and humorous. If you can hold on to your good sense of humour at all times, you are the kind of person we are looking for.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Practicalities

Qualification: Students in their first or second year of their master studies.

Period: The internship position is a full-time position for 6 months.

Start date: 15 August 2014

Contact
For further information, please contact Julie Ebdrup Thomsen on + 45 3079 7359.

Deadline
26 May 2014.

Denmark - Måløv Business Support
09-Apr-2014 Business Analyst
Novo Nordisk is one of the world’s most successful pharmaceutical companies with a great growth potential. Do you want to be part of ensuring that this growth happens in full financial control? ...

Business Analyst

  • Finance
  • Denmark - Bagsværd

Novo Nordisk is one of the world’s most successful pharmaceutical companies with a great growth potential. Do you want to be part of ensuring that this growth happens in full financial control?

About the department
Corporate Financial Planning is part of Corporate Finance (500 employees) and is responsible for the financial management of Novo Nordisk with a close link to the business worldwide. Our aim is to be the best finance operation in the global pharma industry. You will be part of a young and dynamic finance team consisting of 40 dedicated employees split into 6 smaller teams. We have close cooperation with the business units and our aim is to act as true business partners based on strong financial competencies combined with a good understanding of the business in which we operate.

The job
You will be the finance partner for one or more of our business units, including supporting the unit(s) on various financial matters. Our key process related responsibilities are to facilitate the budget process in the areas and provide monthly follow up to senior management. You might also be invited to attend the management meetings as their financial advisor. Furthermore, in order to optimize the financial development within your area of responsibility, you will be involved in various projects and ad hoc analysis.

Qualifications
The person we are looking for has 0-2 years of relevant experience and has completed a relevant master's degree (i.e. in finance or economics) with excellent results. You have strong analytical skills, are computer literate and ready to invest time and effort in your development and future career. Furthermore, it is important that you have good communication skills, including being fluent in written and spoken English as well as being able to communicate with people at all levels of the organisation. The atmosphere in Corporate Financial Planning is informal and humorous. If you can hold on to your good sense of humour at all times, you are the kind of person we are looking for.

We invest a lot in both professional and personal development and have an individualised development plan for each employee. Through on-the-job training, projects and courses you will experience a continued steep learning curve, thus enabling a number of future career opportunities in the global Novo Nordisk organisation.

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Kolos Kopcsai on +45 3079 0809.

Deadline
27 April 2014.

Denmark - Bagsværd Finance
09-Apr-2014 Development Engineer
Skilled mechanical engineers! Boost your career in one of the world’s leading companies within medical devices - located in the greater Copenhagen area. Join Device Research & Development at Novo Nordisk A...

Development Engineer

  • Research & Development
  • Denmark - Hillerød

Skilled mechanical engineers! Boost your career in one of the world’s leading companies within medical devices - located in the greater Copenhagen area.

Join Device Research & Development at Novo Nordisk A/S for a life-changing career!

Novo Nordisk A/S, a global healthcare company with 90 years of innovation and leadership in diabetes care, is looking for skilled engineers for mechanical development.

About the department
Device Research & Development, located in Hillerød, is an area within Global Research & Development, responsible for the development of medical devices for self-treatment within all business areas of Novo Nordisk A/S. Device Research & Development has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. In Device R&D we are determined to develop devices that make a positive difference for our end users whether they are patients, nurses or doctors. You will join a project team of highly skilled engineers and designers, responsible for the development of a new generation injection device to support treatment of chronic diseases.

To learn more about Device Research & Development, please visit: www.novonordisk.com/device-rd

The job
As our new Mechanical System Engineer, you will become a member of mechanical development team that are currently maturing a new device concept for future production.

You will be a part of a cross-functional team and work from the mid to late phases of our product development projects. Your main focus will be to perform system analysis and interface specification, plan and report design verification and validation.

Your contribution will be in all of these areas which entails that your work day is dynamic and rarely the same as the previous. Developing medical devices require a high level of documentation which will be a time consuming task in some periods.

You will be given a number of different responsibilities and experience a variety of tasks, working with both internal and external stakeholders. The job will enhance your professional and personal development, providing you with an opportunity to develop skills within specialist expertise and project management.

Qualifications
You hold an academic degree with at least 5 years of experience within mechanical development. You have worked with mechanical design of plastic components, you master CREO and you are skilled within mechanical disciplines like tolerance stack-ups, material selection as well as kinematic and structural analysis. You have the ability to analyse and understand complex structures and systems.

You are a team player by nature with the ability to work independently with a result-oriented ‘can-do’ attitude. You have a solid academic background with an international profile and must be able to learn fast, excel at cross-functional collaboration and communicate at all levels. You must be prepared to invest significant personal effort in your work and proactively take ownership of your areas of responsibility. You find the role as project coordinator or project manager appealing, and have considered that it might be a future path for you to follow. Proficiency in oral and written English is essential.

At Device Research & Development we use our skills, dedication and ambition to help people with chronic diseases, and change their lives. You will get the opportunity to take part in this, and in addition enhance your career, benefiting from the possibilities for professional and personal development provided by Novo Nordisk A/S.

Device R&D is an organisation with many international employees and we welcome non-local applicants. We have great experience helping people move to Denmark and will support relocation.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please contact Jakob Wielandt on + 45 3075 8881 or Mikkel Larsen on + 45 3075 7410.

Deadline
4 May 2014.

Denmark - Hillerød Research & Development
08-Apr-2014 Senior Risk Advisor
Would you like to drive enterprise risk management in a truly global organisation? Do you strive on combining cross-functional business understanding with financial acumen to identify and scope organisational c...

Senior Risk Advisor

  • Finance
  • Denmark - Bagsværd

Would you like to drive enterprise risk management in a truly global organisation? Do you strive on combining cross-functional business understanding with financial acumen to identify and scope organisational challenges and develop solutions? Do you have a flair for providing high quality business support to and interacting with stakeholders at Senior Management level? If so, this position may be what you are looking for!

About the Department
The Risk Office, located as part of the Corporate Financial Planning, is the secretariat of the Risk Management Board, consisting of Senior Management and chaired by the CFO. We are a young and dynamic team of four, responsible for driving Novo Nordisk’s Enterprise Risk Management system, and we are currently looking for a Senior Risk Advisor who can bring relevant experience and insight to help us continue delivering superior business support to our organisation and stakeholders.

The job
You will be responsible for driving the overall ERM system and the quarterly risk reporting process in your areas of responsibility. This will require you to work closely with different parts of the organisation to ensure that relevant risks are identified and assessed, and act as a sparring partner. To accomplish this task successfully, you will be required not only to have a profound understanding of the value chain activities, but also to utilise it actively to raise relevant discussions on risk content and bring insights to different stakeholders.

You will also be responsible for conducting and facilitating relevant risk workshops with Senior Management teams and other stakeholders. This is a crucial task that allows us to maintain momentum in the risk organisation and secure strong risk anchoring.

Finally, you will drive and contribute to a variety of interesting risk projects, which are normally carried out in cooperation with stakeholders and colleagues from a variety of organisational functions and aim at supporting and enhancing different parts of the ERM system and/or risk reporting process.

In the Senior Risk Advisor role, you will gain excellent insight into the global Novo Nordisk organisation and will get an opportunity to work on truly cross-functional projects. You will also be exposed to all activities in the Novo Nordisk global value chain, which will enable you to develop unique business understanding and establish a broad network in the organisation.

You will be physically located in the Novo Nordisk headquarters in Bagsværd, Denmark. However, some international travel will be required.

Qualifications
You hold a master’s degree in business, chemistry, supply chain, production, quality, engineering or similar, and your career so far has provided you with in-depth experience and knowledge related to your area of expertise. You possess strong analytical and strategic thinking capabilities, and can solve complex problems fast.

You have strong facilitation, communication/presentation and stakeholder engagement skills and connect easily with others. In this job, solid interpersonal and leadership skills are a must, and so is intercultural awareness and sensitivity.

Last but not least, you have a sense of humour and are praised by your peers as a dedicated and hard-working colleague. You are fluent in spoken and written English, and have strong PC skills (incl. MS Office).

At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please call Annette Fiig on + 45 3079 6962.

Deadline
27 April 2014

Denmark - Bagsværd Finance
08-Apr-2014 QA Chemist
Would you like to help securing release of Novo Nordisk A/S Glucagon? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biophar...

QA Chemist

  • Quality
  • Denmark - Gentofte

Would you like to help securing release of Novo Nordisk A/S Glucagon? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biopharm QA Aseptic Production.

About the department
Biopharm QA AP is responsible for quality assurance of three existing aseptic filling plants and the building of a new filling plant, two laboratories and all utility systems in the Gen-tofte production areas. Our key tasks are to review and approve all sorts of GMP docu-mentation such as validation reports, change requests and non-conformities and batch documentation in order to be able to release filled product for packaging.

As QA Chemist in Biopharm QA AP you will join a group of highly skilled and competent colleagues working in five teams lead by separate associate managers. By joining us you will get the chance of professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry.

The job
The position is situated in Gentofte in one of our releasing teams for filling plants. The team consists of 12 chemists. The job includes QA review of several types of documents hereunder batch documentation to ensure release of Glucagon. The documents come from all types of processes thus guaranteeing a high level of variety on a daily business.

Your main responsibility will be to quality assure the release of Glucagon. And thereby contribute to assure product quality and compliance with the current GMP rules and guidelines. On top of that QA is a major player at internal audits and external authority inspections, where you are expected to participate.

When started you will undergo an individual and intense training program, where you can expect to be given more responsibility gradually.

Qualifications
You hold an academic degree that qualify you as QP (Qualified Person) according to the Danish Medical Agency. Preferable your academic background is topped with experience either from the pharmaceutical industry. However we would also like to hear from talent-ed newly academic graduates.

It is important that you thrive in a role where you are required to take independent deci-sions and show a high degree of authority. You have a strong quality mind-set and you are robust. You know and meet your deadlines and you are capable of prioritising between different tasks in a dynamic environment. You are a dedicated team player who inspires trust and respect amongst colleagues and partners. Your language skills cover proficiency in both Danish and English.

Your application is welcome in Danish or English.

Contact
For further information, please contact Rune Goldschmidt Ruders at +45 3075 5361 or Rikke Wissing Jensen at +45 3075 1566.

Deadline
25 April 2014.

Denmark - Gentofte Quality
08-Apr-2014 QA Chemist
Would you like to help securing release of Novo Nordisk A/S products from different pro-duction facilities in Gentofte? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you...

QA Chemist

  • Quality
  • Denmark - Gentofte

Would you like to help securing release of Novo Nordisk A/S products from different pro-duction facilities in Gentofte? Do you thrive when working in a team; handling multiple tasks of high complexity? Then you might be the person we are looking for in Biopharm QA Aseptic Production.

About the department
Biopharm QA AP is responsible for quality assurance of three existing aseptic filling plants and the building of a new filling plant, all utility systems in the Gentofte production areas and all equipment and facility qualification activities. Our key tasks are to review and ap-prove all sorts of GMP documentation such as change requests, non-conformities, valida-tion and qualification protocols and reports (IQ, OQ, PQ) in order to secure a stable plat-form for the continuous release of filled product.

As QA Chemist in department Biopharm QA AP you will join a group of highly skilled and competent colleagues working in four teams lead by separate associate managers. By joining us you will get the chance of professional and personal development and you will get an excellent and unique overview of current authority expectations and demands in the pharmaceutical industry.

The job
The position is situated in Gentofte and the team consists of 12 chemists. The job includes QA review of several types of documents with special focus on qualification activities regarding production equipment and facility. The documents come from all types of processes thus ensuring a high level of variety on a daily basis.

Your main responsibility will be to quality assure qualification activities hereunder instal-lation and operational qualification. Thereby contribute to assure product quality and compliance with the current GMP rules and guidelines. On top of that QA is a major player at internal audits and external authority inspections, where you are expected to partic-ipate.

When started you will undergo an individual and intense training program, where you can expect to be given more responsibility gradually.

Qualifications
You hold an academic degree as an engineer, pharmacist or alike. Preferable your aca-demic background is topped with qualification experience from the pharmaceutical indus-try. However, we would also like to hear from talented newly academic graduates.

It is important that you thrive in a role where you are required to take independent deci-sions and show a high degree of authority. You have a strong quality mind-set and you are robust. You know and meet your deadlines and you are capable of prioritising between different tasks in a dynamic environment. You are a dedicated team player who inspires trust and respect amongst colleagues and partners. Your language skills cover proficiency in both Danish and English.

Your application is welcome in Danish or English.

Contact
For further information, please contact Rune Goldschmidt Ruders at +45 30755361 or Rikke Wissing Jensen at +45 3075 1566.

Deadline
25 April 2014.

Denmark - Gentofte Quality
08-Apr-2014 Corporate Process Expert for the Quality Risk Management process
Do you possess experience and in-depth knowledge within Quality Risk Management? Do you have a proven record in planning and delivery of process improvements? Can you take a corporate leadership and are you use...

Corporate Process Expert for the Quality Risk Management process

  • Quality
  • Denmark - Bagsværd

Do you possess experience and in-depth knowledge within Quality Risk Management? Do you have a proven record in planning and delivery of process improvements? Can you take a corporate leadership and are you used to communicate complex issues in an easily understandable way? - then go for this job!

About the department
Quality Capability Development (QCD) is part of the Corporate Quality organisation in Novo Nordisk. We are a small team of process experts responsible for ensuring compliance to external requirements and continuously improving a number of quality processes under our responsibility to the benefit of all our stakeholders in Novo Nordisk. The department is located in Bagsværd, Denmark.

The Job
As the Quality Risk Management (QRM) Process Expert in Novo Nordisk, your primary job will be to ensure that Novo Nordisk stays in compliance with external requirements, to set strategic direction for the QRM process, to continuously improve the way we work, to communicate relevant issues at all levels in the organisation and to secure more efficient and effective processes across Novo Nordisk globally. As the corporate Process Expert you will establish and drive a small network of local QRM experts from LoB. Your role will be to ensure development of QRM operational standards, prepare and describe tools and guidance, deliver training including the QRM Facilitator training programme, prepare and deliver a process strategy, establish process KPIs and follow-up on process performance etc. You will furthermore be expected to deliver compliance support within QRM to LoB e.g. during audits and inspections.

In Novo Nordisk we are currently strengthening our process orientation and you will be a key player in implementing and maturing the process management in the QRM process in close cooperation with the Process Owner Delegate.

Qualifications
You have an academic background e.g M.Sc. and a solid and up-to-date experience within QRM. It is important that you have an in-depth understanding of QRM related external requirements and hands-on experience with interpretation, implementation and practices most likely from some years of experience in a Pharmaceutical or Medical Device company. You may have a formal Project Manager education, but more importantly you have a proven record of driving continuous improvements activities to implementation in an international organisation and as such have the needed competencies to impact the organisation at all levels. You are an enthusiastic and committed person with personal assertiveness and ability to take leadership and motivate others. You are experienced in working and communicating with people at all levels in the organisation. You are required to communicate fluently in English and preferably in Danish and you must be able to present complex matters in a simple way. You are service-minded, enterprising, independent and persistent. We are determined to continuously improve our work and it is therefore important that you are able to see opportunities instead of limitations and can achieve results.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For additional information, please contact Mette Fjord Andersson on + 45 3079 4692.

Deadline
11 May 2014.

Denmark - Bagsværd Quality
08-Apr-2014 Internship
At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities f...

Internship

  • Marketing
  • Denmark - Køge

At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort. Our internships provide exciting learning opportunities for students who bring new ways of thinking to our company.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

About the department
This is an exciting opportunity to join an international, high performing team in Køge, Denmark. You will work with the marketing department in the implementation of the 2014 marketing initiatives. You will work in close collaboration with the sales organization in ensuring we establish the correct strategies and approach in the market.

The job
You will assist the marketing communication team targeting key global. In this role you will perform targeted literature searches to address strategic questions, help to develop/ensure timely updates to our internal tools, work with team members to develop new marketing strategies, and assist with value communication planning/development. E.g. Flyers design, Newsletter support, Market data evaluation, Market research, plus the ability to create content for all marketing material.

Qualifications
You are a university student in Life sciences with focus on Biopharmaceuticals with a scientific knowledge of the cell culture media.

You are currently studying on your master’s degree in Life sciences and have a deep knowledge of the cell culture media. We expect candidates to be service minded, thrive in a busy environment and bring a can-do attitude. Fluency in both oral and written English, sound personal judgment, and excellent interpersonal skills are required.

You are an outgoing person with a strong personal drive and dedication. You have professional and personal impact that is reflected in your desire to take initiative. In addition, you thrive in a busy environment and bring a can-do attitude and a healthy sense of humour to your work – even when the pressure is on. Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

Practicalities
Students in their first or second year of their master studies. The internship position is a full-time position for 6 months.

Contact
For further information, please call Vanessa Leon on +45 5667 1091

Deadline
2 June 2014

Denmark - Køge Marketing
08-Apr-2014 Drug Product Coordinator
Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is ex...

Drug Product Coordinator

  • Research & Development
  • Denmark - Måløv

Are you looking for new challenges within formulation, process or analytical method development of solid dosage forms and do you want to make a difference? Our Oral Protein Formulation Unit (OPF) in Måløv is expanding therefore we are looking for several dedicated, professional and enthusiastic new colleagues. Novo Nordisk is on a voyage towards the development and production of oral formulations of proteins. Our ambition is to develop break-through products based on orally available versions of insulin and GLP-1. You will be involved in CMC activities for formulation/process development, pilot production, scale-up and analysis of solid protein dosage forms towards clinical trials.

About the department
We are 26 scientists and technicians in Oral Formulation & Process Development organized in two teams. The Department is overall responsible for development of Solid Dosage Forms of Insulin and GLP-1 molecules for oral delivery. The formulation development covers from early phase development of oral protein formulations and processes in small scale to later stages of formulation development with larger scale. In the later phase the progress towards robust manufacturing processes is of critical importance. The formulation development is done using rational design, statistical and QBD principles.

The job
We are looking for an experienced Drug Product Coordinator to coordinate oral product portfolio projects.

As a Drug Product Coordinator you will be responsible for aligning the project organisation needs with those of the Line of Business. You will be part of the cmc core project team along with the other technical coordinators e.g. API and analysis as well as collaborate closely with the departmental oral product development groups. In this dual role you will define specific department activities linked to the overall project key deliverables. Close collaboration with the line management of the departments is vital in order to ensure the most optimal planning and execution of project targets.

More detailed responsibilities include: Breakdown of project key deliverables to department activities in our primary project planning system. Plan the timing of department activities together with department team leaders and other project coordinators. Communicate risk based development and pilot manufacture scenarios to the project core group. Clear and timely communication of project requirements to team and department members. Prepare and coordinate regulatory documentation according to international guidelines. Drive continuous improvements using LEAN/Six Sigma approach.

Qualifications
The person we are looking for ideally has 3-5 years of experience in managing CMC activities covering early to late phase clinical development. Detailed knowledge of the pharmaceutical value chain is a must as well as excellent knowledge of the CMC documentation flow.Scientific experience with Solid Dosage Form drug development and manufacture is a great advantage for the candidate as is knowledge in protein analysis, characterization and formulation

A MSc or PhD education level in a relevant scientific field is compulsory in order to become a successful applicant for the position.

As a person we expect you to have excellent collaboration skills, be structured and reliable and to have an ability to keep your cool and make the right decisions in a hectic work environment. Also, you are a team player and have a feel for communicating essential information to the right stakeholders at the right time.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information please contact Lone Løgstrup Kimer at +45 3079 3569.

Deadline
30 April 2014.

Denmark - Måløv Research & Development
07-Apr-2014 Sr. Project Coordinator
We are currently looking for a Project Coordinator with an interest in and experience with, the development of the design of printed packaging materials, and coordination of labelling launch activities. ...

Sr. Project Coordinator

  • Regulatory Affairs
  • Denmark - Søborg

We are currently looking for a Project Coordinator with an interest in and experience with, the development of the design of printed packaging materials, and coordination of labelling launch activities.

About the department
Labelling Development and Launch is part of Regulatory Affairs, which makes medicine available to patients all over the world by ensuring rapid regulatory approval in all markets.

You will join nineteen skilled and motivated colleagues in Regulatory Labelling Development and Launch. The department is responsible for the printed packaging material development and launch projects. We drive the development of printed packaging material designs for all new Novo Nordisk products and life cycle management projects, and we ensure timely market launch of printed packaging materials for all Novo Nordisk products globally. The permanent position is located in Søborg, Denmark.

The job
As a Project Coordinator your primary task will be to independently drive and coordinate projects, both with regards to secondary packaging development and launch activities.

Your job will be to set the right direction for the project and, at the same time, ensure that your project is implemented and anchored in the organisation. The projects will vary in size and complexity, but will all be cross-organisational. You will ensure delivery of results on both printed packaging material projects and launch activities according to the overall project plans. You will be responsible for thoroughly creating, storing, and archiving the relevant documentation for project activities and decisions according to Good Documentation Practices and internal procedures. You will work together with many stakeholders on a cross functional level.

Qualifications
You have completed a relevant Master's Degree (Masters of Science, Engineering, or other) with excellent results, and have at least 3 years’ experience from the pharmaceutical industry. You have acquired solid experience within project management. You are comfortable interacting with stakeholders at any organisational level and are used to working across organisational and geographical boundaries. Leading others in project contexts comes natural to you, and you use your energy and understanding of other people to involve the right competencies in the right processes and carry projects ideas through with success. Development of packaging material is a fast moving field where new requirements constantly emerge. Therefore the position requires a good understanding of e.g. design controls and human factors engineering.

You are able to work very independently and have a high level of drive, initiative and persistence. You are result-oriented, ambitious, and like to be challenged. You are analytical, structured and comfortable managing a team on your own. You are proficient in Office applications. An excellent command of our corporate language, English, is a must, and knowledge of Danish is an advantage.

In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer our employees opportunities for continuous growth.

Contact
If you have any questions about the position, please contact Bente Jessen on +45 3075 8056.

Deadline
25 April 2014.

Denmark - Søborg Regulatory Affairs
04-Apr-2014 QA Engineer
Would you like to work in an international environment and be responsible for the quality assurance of components produced internally in Device Manufacturing Sourcing (DMS) on site Hillerød? Are you ready to ta...

QA Engineer

  • Quality
  • Denmark - Hillerød

Would you like to work in an international environment and be responsible for the quality assurance of components produced internally in Device Manufacturing Sourcing (DMS) on site Hillerød? Are you ready to take high impact decisions regarding the right level of quality to ensure patient safety? Then you might be the person we are looking for.

About the department
We are looking for a dedicated person with a high quality mind-set who will be part of the Manufacturing Quality Assurance team of 10 QA engineers. We are responsible for the quality assurance of all components produced internally in Novo Nordisk delivered for production of medical devices worldwide.

The job
As a QA engineer you will be responsible for ensuring and developing quality and compliance of the current production in DMS. You will make sure that our quality systems follow Novo Nordisk regulations, legal requirements, GMP, and ISO standards. You will review SOP documentation, write and approve change requests as well as approving non-conformity investigations. You will be part of a team with other experienced colleagues and have good opportunity for sparring. You will participate in investigations of root causes to non-conformities and customer complaints. In your daily work, you will interact with and be sparring partner for several departments such as Q-Support, Logistics, Quality Control, Mould and Pre-assembly production. You have direct access to the moulding and pre-assembly production and your success will depend on your ability to collaborate and communicate with all types of colleagues and business partners. Quality Mind-set and winning culture are incorporated concepts of our daily work.

Qualifications
First and foremost you have an excellent quality mind-set, good communication skills and you can place the importance of compliance on the agenda in a positive and constructive way.

You hold an academic degree and you preferably have 3-5 years of experience with quality assurance from the pharmaceutical, medical device or similar industry. It is an advantage if you have experience with ISO13485 or GMP, and Lean. Furthermore process insight in injection moulding and assembly production will be preferred.

Your language skills cover proficiency in English and Danish. You are known for finding constructive solutions as well as taking responsibility for your assignments. You enjoy the mixture of routine tasks and more challenging tasks, and you are flexible to changes in workload. Additionally, you work independently and you make decisions regarding quality tasks ensuring the right balance between quality demands, authority demands and business needs. You are structured and a team-player.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information, please call Lili Behjat Kristensen at +45 3079 4143.

Deadline
27 April 2014.

Denmark - Hillerød Quality
04-Apr-2014 Senior Programmer for Biostatistics Programming Anchor
Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual developme...

Senior Programmer for Biostatistics Programming Anchor

  • Research & Development
  • Denmark - Søborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual development and influence on decision making?

Do you wish to work in a highly professional, engaged and global environment, where you can use your programming skills and quality mind-set bringing clinical projects to registration and market? You may be our new senior statistical programmer.

About the department
The Biostatistics Programming Anchor consists of 8 enthusiastic statistical programmers and process development specialists. The team is responsible for development and support of clinical data standardisation and reporting, planning and conduct of training within systems and processes, and maintenance and improvement of programming processes.

The team is part of Novo Nordisk’s large Biostatistics function with 150 statisticians and statistical programmers globally in our R&D clinical development organisation. Biostatistics is a dynamic department which cooperates with many different professionals in the organisation both within Denmark and across borders with our affiliates in the US, India, China and Japan, as well as our outsourcing partners in India. The job is situated in Copenhagen.

The job
As senior statistical programmer you will be involved in maintenance and development of SAS standard programs for reporting of clinical data. You will take part in system development and process improvement projects within statistical programming and you will give input to maintenance of global clinical data standards and data models Furthermore, you will be an active trainer and supporter in the global Biostatistics organisation.

You must take responsibility for both standard tasks and more complex and time critical tasks. Development of methods and processes, as well as knowledge sharing is continuously ongoing in Novo Nordisk, especially based on the initiative of the employees. Therefore we expect you to communicate programming/technical problems and ideas both internally and externally.

We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we offer great opportunities for ongoing training to ensure the continued competency development of our employees.

Qualifications
You have a B.Sc. or M.Sc. within IT, natural sciences or other relevant degree, extensive knowledge and experience with SAS programming, IT system development methodologies, CDISC and clinical data domains. You have preferably five to eight years’ experience within clinical research and are able to write efficient, well documented and standardised computer programs. Furthermore, strong cooperation and analytical skills are a necessity. You are capable of working independently, take on responsibility and show initiative.

We expect you to be flexible and efficient. In addition we expect you to be able to overview several challenging tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. Experience with project management and being a trainer will be an advantage.

Good collaboration and communication skills are necessary characteristics. You are also fluent in English.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Gert Bech Alding on + 45 3075 4892 or Tina Christiansen on + 45 3079 1748.

Deadline
27 April 2014.

Denmark - Søborg Research & Development
04-Apr-2014 Senior Programmer Biostatistics Copenhagen or Aalborg
Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual developme...

Senior Programmer Biostatistics Copenhagen or Aalborg

  • Research & Development
  • Denmark - Søborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, which ensures huge variety of tasks, great opportunities for individual development and influence on decision making?

Do you wish to work in a highly professional, engaged and global environment, where you can use your programming skills and quality mindset bringing clinical projects to registration and market? You may be one of our new statistical programmers.

About the department
The Biostatistics function is growing and consists currently of 150 statisticians and statistical programmers globally in our R&D clinical development organisation. Biostatistics is a dynamic department which cooperates with many different areas in the organisation both within Denmark and across borders with our affiliates in the US, India, China and Japan, as well as our outsourcing partners in India. Biostatistics provides a strong scientific community and we are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

The job
As senior statistical programmer your primary responsibility is to develop SAS programs based on clinical data for reporting of clinical trials, preparing summary documents and publications as well as supporting regulatory commitments. You handle many assignments concurrently and will work in close collaboration with a team of statisticians and statistical programmers.

You will be involved in coordinating and supervising the work of contract houses around the world performing outsourced programming tasks. Therefore we expect you to communicate programming/technical problems and ideas both internally and externally, as well as coach more junior colleagues. You must take responsibility for both standard tasks and more complex and time critical tasks.

Development of methods and processes, as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in the maintenance of Biostatistics as a good and challenging place to work. In exchange we of course offer great opportunities for on-going training to ensure the continued competency development of our employees. The job can be situated in Søborg or in Aalborg.

Qualifications
You have a B.Sc. or M.Sc. within science, IT or other relevant degree, extensive knowledge and experience with the SAS programming language, as well as preferably experience within clinical research. You are able to write efficient, well documented and standardised computer programs. Furthermore, strong cooperation and analytical skills as well as an understanding for data structure are a necessity. You are capable of working independently, take on responsibility and show initiative.

We expect you to be independent and that you are flexible and efficient. In addition we expect you to be able to overview several challenging tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. Experience with project management will be an advantage.

Good collaboration and communication skills are necessary characteristics. You are also fluent in English.

At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please call Birgitte Hylleberg Svendsen on + 45 3079 2510 or Malene Højbjerre on + 45 3079 6209.

Deadline
27 April 2014.

Denmark - Søborg Research & Development
02-Apr-2014 Internship in FLIR Consulting
Novo Nordisk is one of the world’s most successful pharmaceutical companies. At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join...

Internship in FLIR Consulting

  • Student and Internships
  • Denmark - Bagsværd

Novo Nordisk is one of the world’s most successful pharmaceutical companies. At Novo Nordisk, we share a passion for changing patients’ lives, and we are always looking for talented individuals who want to join us in this effort.

FLIR Consulting (Finance, Legal, Investor Relations) is an internal consultancy reporting to our CFO. We support the organisation by driving a number of key strategic projects throughout Novo Nordisk’s global operations.

Our internships provide exciting learning opportunities for master’s degree students who bring new ways of thinking to our company.

About the department
You will be part of a young, diverse department consisting of 12 dedicated employees with backgrounds from top-tier consultancies (e.g. McKinsey & Co, Bain & Co, etc.) or with previous Novo Nordisk experience.

The internship offers your first-hand experience of working with some of the best strategy consultants, and will provide you a steep learning curve with exposure to best practice project management methods and tools.

The job
As an intern in FLIR Consulting, you will participate in various projects as a junior consultant together with more experienced project members. Your tasks will vary widely, and include analyses, information gathering, participating in team problem solving, and independently driving own work streams.

Qualifications
You are among the best in your class and take an interest in consulting, corporate finance and project management. You are a master’s degree student in Economics, Business Administration, Engineering or similar in the first or second year of your studies. You are fluent in English, and are used to both working independently and in teams. Finally, you have excellent problem solving skills and a positive attitude.

Your development is important to us. Training and personal development are key tools to ensure continuing development of your toolbox.

Practicalities:

Period: The internship position is a full-time position for 5-6 months

Start date: 1 August 2014

Contact
For further information, please call Nina Correll on + 45 3075 5009.

Deadline
1 May 2014.

Denmark - Bagsværd Student and Internships
02-Apr-2014 PostDoc Fellow for a Pharmacoepidemiologic Research Project
Novo Nordisk is participating in the European GetReal project, under the Innovative Medicines Initiative (IMI). IMI is Europe's largest public-private research program aimed at optimizing the development of bet...

PostDoc Fellow for a Pharmacoepidemiologic Research Project

  • Research & Development
  • Denmark - Mørkhøj/Søborg

Novo Nordisk is participating in the European GetReal project, under the Innovative Medicines Initiative (IMI). IMI is Europe's largest public-private research program aimed at optimizing the development of better and safer medicines for patients (http://www.imi.europa.eu).

We are looking for a PostDoc fellow to join the Health Economics & HTA department and work on the GetReal project for a 12 months period with possibility for extension.

About the department
The Health Economics & HTA department is part of Global Development, caretaking all clinical development projects in Novo Nordisk. Health Economics & HTA is responsible for health economic input to project in the Novo Nordisk’s R&D pipeline and the department consists of 12 experienced health economists with a diverse background. You will report to the Director of Health Economics and HTA and work closely with the project lead for the GetReal project. The department is responsible for generating evidence that support the value of the Novo Nordisk development products. You will have cross-functional interactions with multiple stakeholders in Novo Nordisk, including Regulatory Affairs, Epidemiology, and other PhD/PostDoc fellows. External stakeholders and partners will be universities, health authorities and other members of the IMI project. Travels will be expected as this is an international collaboration.

The job
The overall objectives of GetReal are (1) for pharmaceutical R&D and healthcare decision makers to better understand how real-world data and analytical techniques can be used to improve the relevance of knowledge generated during development, e.g., through innovation in clinical trial design, and (2) to develop tools to better predict the effectiveness of a drug, before launch. Designs of studies with electronic health care databases and pragmatic trials will be proposed. Furthermore you will be looking at how to deal with a more flexible experimental design: dynamic exposure, adaptive designs, etc.

The work is related to one of the work packages of the GetReal project and includes collaboration with universities in the Netherlands and in the United Kingdom. The specific work package aims at identifying key drivers of effectiveness to understand why and to which extent efficacy differs from effectiveness and to provide tools to address this gap. The postdoc will work on how more “pragmatic” clinical trials before launch can be performed and analyse electronic health care databases, do literature reviews as well as looking at pragmatic trial designs.

You will be responsible for collaboration between Novo Nordisk and the universities in the work package. You will ensure that the work is in line with the scope of the project, from an R&D perspective.

You will fully participate in the elaboration of the protocols for pilot studies, the execution of the pilot studies and the publication of studies.

Qualifications
You have a PhD degree from Public Health sciences, epidemiology, pharmaco-epidemiology or Health Economics and advanced knowledge about statistical methods.

On the personal side, strong communication skills and analytical skills are needed, as well as a proven ability to work independently and efficiently with various external and internal stakeholders.

Practicalities

Period: The position is a full-time position for 1 year. The project runs until end of 2016, and it will be possible to extend if expectations on both sides are met.

Start date: 01 May 2014 or later.

Contact
For further information, please call Mark Aagren on + 45 30799976 or Erpur Adalsteinsson on + 45 30751737.

Deadline
25 April 2014.

Denmark - Mørkhøj/Søborg Research & Development
01-Apr-2014 Category Management
Do you have a strong business mind-set and are you looking for a job with the possibility to further develop your skills and competences within category management, market and spend analysis, stakeholder manage...

Category Management

  • Sourcing
  • Denmark - Bagsværd

Do you have a strong business mind-set and are you looking for a job with the possibility to further develop your skills and competences within category management, market and spend analysis, stakeholder management, negotiations and contracting.

About the department
Corporate Procurement is, in close cooperation with affiliates and stakeholders, responsible for purchasing, sourcing and contracting of the global indirect spend in Novo Nordisk. Corporate Procurement has more than 100 employees and is anchored in the Corporate Finance organisation. You will be part of a dynamic and enthusiastic group of 6 team members in the Marketing Services team. We are part of Marketing, Professional & Travel Management Services Department and hold the responsibility for the marketing related service categories.

The Job
As Associate Category Manager you will have a variety of operational sourcing tasks and act as commercial anchor-point between our suppliers and our organisation. Amongst others the tasks include: support creation of a sourcing pipeline of upcoming marketing projects, conducting structured tender processes in accordance with the standard Novo Nordisk sourcing model, support on contract negotiations and compliance related tasks and establishing strong stakeholder relationships across our global organisation. On larger projects you will team up with senior colleagues to support you professionally and to drive your personal development.

You will also be involved in the establishment and implementation of category strategies including: business and market intelligence facilitating fact-based decision making, incl. development of cost models, excellent supplier relationship management and ensuring value creation for different business areas across Novo Nordisk in line with category strategies.

Qualifications
The ideal candidate has 2-5 years working experience. We expect you to have a relevant Master degree with excellent results and a track record of strategic sourcing of professional services – preferably within marketing related services. You possess a combination of project management and strong analytic capabilities, together with excellent people skills and lots of humour. You are able to advise senior stakeholders on best sourcing practices as well as on commercial aspects during negotiations. The ideal candidate has experience from or interest in negotiation of both specific delivery contracts and frame agreements

As a person you are ambitious and a proactive self-starter driven by achieving the best possible results while acti