QA validation professional

• Quality
• Denmark - Hillerød

Do you want a key role in ensuring the quality of the insulin products and compliance with regulatory requirements? If so, then seize the opportunity and join QA of the aseptic production (AP) and quality control (QC) in Site Denmark.

About the department
In QA AP/QC we are responsible of assuring quality and compliance in the AP of insulin products and QC in Site Denmark. It is our responsibility that the documentation related to AP and QC is in compliance with regulatory requirements and the Novo Nordisk quality management system.In QA AP/QC you will join a department of 46 highly motivated and dedicated employees which is divided in three teams - two teams in Bagsværd and one team in Hillerød. In a close collaboration with the production and QC we ensure a high level of quality and play a key role in releasing insulin products to diabetics all over the world. We are at the moment looking for a QA validation professional (permanent position) to our team in Hillerød.

The Job
As a QA validation professional you will be a decisive factor in making sure that the released products lives up the current GMP and regulatory requirements. You will be involved in qualification and validation of equipment and processes as well as the handling of incidents in the production and QC laboratories. Likewise, you will perform different tasks related to quality assurance, e.g. approval of laboratory investigations and change requests. We operate in a LEAN environment where we focus on optimising our processes. You will therefore be involved in the implementation of new initiatives which can optimise our daily work.

Qualifications
You hold an academic degree and your academic background is topped with at least 5 years of relevant experience from the pharmaceutical industry working with validations and projects. Preferably, you have from previous jobs experience from QC. On a personal level you are known for you positive mindset, flexibility and persistence. You have a strong quality mindset, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. You like and are good at coordinating different tasks for both yourself and other people and you demonstrate an ability to find the right solutions with your colleagues. Your language skills cover proficiency in both Danish and English.

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 Morten Petersen,at +45 3075 0663.

Deadline
16 June 2013

Compliance Project Manager

• Quality
• Denmark - Søborg

Are you a competent change agent? Can you win acceptance for enhanced business processes from stakeholders in a complex production environment? Then we could have the vacancy for you as Compliance Project Manager in Diabetes Finished Products (DFP).

About the department
You will join our brand new Compliance team of 3 skilled colleagues specialised in quality compliance and business optimisation in DFP Compliance Support. We provide support to all DFP sites to secure that our processes to ensure compliance are as efficient as possible. As we support sites from Denmark, China, France, Brazil and the USA, you will be working across national borders and different working cultures.

The Job
Your job will be to optimise complex business processes across business areas such as quality, manufacturing development and production in DFP and Product Supply. Specifically, you will drive various projects that seek to continuously optimise our compliance level, e.g. by improving the processes we use to implement new requirements in our quality management system and on the shop floor. An important part of your job will be to track compliance and report the status to the senior management on a regular basis. You will also communicate the findings from audits and inspections to the sites and follow up on the implementation accordingly. In all your work you secure alignment with your stakeholders at all levels – from Operators to Vice Presidents.

Qualifications
You hold an MSc within a business-related, pharmaceutical or engineering discipline. Your educational background is supplemented with solid experience from a job as Business Analyst or similar. This has provided you with competences to drive projects from a-z – preferably in an international setting. In other words, you know how to facilitate change management in a complex business environment, and if you have insight into a quality management system, it will be appreciated. You have excellent analytical skills, and you can easily comprehend larger piles of data, extract the essences, and interpret and present these in a clear way. It is important you thrive in a job where you work with documentation on a daily basis. Coordinating many simultaneous tasks, you will need a structured approach, and you thrive performing independently relying on your high level of drive to create sustainable results. As you will interact with an array of different stakeholders, you need an open mind and outstanding communication skills.

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 Ida Bøkman at +45 3075 1282.

Deadline
9 June 2013

Project Manager

• Project Management
• Denmark - Hillerød

Device, Manufacturing & Sourcing (DMS) in Hillerød is looking for a Project Manager, who can manage projects across functional as well as geographical boundaries.

The mission of DMS in Hillerød is to manage the global supply chain of moulded components and preassembled parts for Novo Nordisk many prefilled devices.

About the department
If you are our new project manager you will be a part of EHS & Project Execution, which consists of 10 project managers. You will be surrounded by talented and dedicated colleagues with whom you can exchange knowledge and develop even further as project manager.

The job
As project manager in EHS & Project Execution you will e.g. be responsible for a package of moulding tools to support our capacity ramp up. The projects are run within the framework of our mature project model. Your main task will be to plan and execute the project work, i.e. risk, scope, schedule, cost, quality. Negotiate project resources with line of business, establish the project team and manage resources to ensure progress and optimal use of relevant competences during project execution.

The project managers in EHS & Project Execution lead some of the highest prioritised projects in DMS, and the team is focused on developing excellent project managers who can manage multiple projects with characteristics of new technology, IT, strategy, product transfer, sourcing and more. Therefore you will also be working with many different people and parts of the Novo Nordisk organisation.

Qualifications
You hold a master degree in engineering, or equivalent. You possess a great business sense and are great at engaging people and set direction to achieve project specified goals. You have minimum 3 - 5 years of relevant project management experience. Furthermore, you possess good interpersonal skills, are process oriented and have the ability to communicate simple and uncomplicated. For us, it is also important you support the rest of the team in creating a positive spirit and a good department. Good communication and documentation skills Danish and in English are necessity. You pay high attention to detail work well alone as well in cooperation with colleagues. On a personal level you are self-motivated, work independently and are a dedicated team player who focuses on quality and results. Obviously you possess an open mind-set required in a global and dynamic 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 Grith Albrecht at +45 3075 8559 or Henrik Fritzbøger Jægerlund at +45 3075 5535.

Deadline
5 June 2013.

Engineer with cleaning experience

• Production
• Denmark - Kalundborg

If you have solid experience from working with cleaning in the pharma industry, you have just the right foundation to be our new colleague – and our expert representative in Novo Nordisk’s cross organisational cleaning competency group.

About the department
You will join Insulin Manufacturing 2 (IM2). We produce API for a number of Insulin finish products. Your closest colleagues will be a group of 6 Chemists and technicians in Utility Support but as expert you will be working across the total production facility.

The job
Your focus will be cleaning validation. As such, you formulate and challenge the cleaning strategies and set the direction for the area. This includes ensuring our cleaning processes, methods and equipment apply with Novo Nordisk’s and the authorities directions and if major changes are needed you handle the change requests.

In addition, you ensure an ongoing optimisation in order to make our workflow and cleaning documentation more LEAN. Another vital part of your job will be systematic hands-on problem solving in the production area when complex issues occurs in close dialogue with the production teams, Quality Assurance, Manufacturing Development and Regulatory Affairs. Finally, you play an important role in inspections and audits, where you are the one who present the cleaning area in a convincing and professional way.

This job is an opportunity to dive even deeper into cleaning and challenge your current knowlegde.

Qualifications
You hold a master’s degree in engineering or similar. Your career has provided you with a broad knowledge within API production including at least 3 years focused experience from cleaning validation. To succeed you must thrive on taking initiatives on your own and comfortable having a major personal responsibility for a very important business area. This also takes the ability to prioritise your tasks and meet deadlines, while remaining attentive to quality and details. You are capable of sharing knowledge at any organisational level, and with your extrovert and proactive attitude you can easily establish a network across the organisation. Working across business areas and with people with very different professions and backgrounds will call for all of your cooperation and communication skills – in Danish and English, written as spoken.

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. We are at the front edge of the development within technology, systems, methods and processes. If you are our new colleague, we can guarantee opportunities that you will have a hard time finding anywhere else.

In Novo Nordisk 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 contact Dorte Rehné at +45 3079 0622.

Deadline
14 June 2013.

International Medical Director

• Research & Development, Medical Doctor
• Denmark - Søborg

The Medical & Science, Inflammation & Growth Hormone (GH) department at Novo Nordisk A/S, is seeking a physician to take on a position as a Medical Specialist to focus within the development and life cycle management of GH. Novo Nordisk is an established leader in GH therapy having been on the market with state of the art products for many years. We have an exciting position available to contribute both to the development of innovative GH therapies and to the life cycle management of GH. The job will require strong interaction with highly engaged colleagues and external stakeholders including therapeutic experts.

About the department
Medical & Science, Inflammation & Growth Hormone consists of 14 employees, part of Global Development located in Søborg, DK, and Princeton, USA. We have overall medical responsibility for Clinical Development Plans in the Inflammation and Growth Hormone area, which currently include the disease areas of Rheumatoid Arthritis (RA), Crohn’s Disease (CD), Systemic Lupus Erythematous (SLE) and Growth Hormone Deficiency and Growth disorders.

The job
The key responsibilities of the successful candidate will be to function as a global Medical Specialist within the Growth Hormone franchise. This includes being instrumental in implementing clinical development and regulatory strategies for drug candidates. The person will be involved in developing Clinical Development Plans, executing and reporting clinical studies phase 1-3 trials, providing medical and clinical expertise to the generation of Product Business Plans and Strategic Product Plans as well as medical deliverables to the paediatric investigational plans for development projects and to life cycle management of GH. Close interaction with health authorities will be an integrated part of the job. The position will be based in Søborg, Denmark.

Qualifications
You have a medical degree including scientific knowledge and some clinical experience relevant to the GH or related therapeutic areas. It will be an advantage if you have previous experience from the pharmaceutical industry including experience in developing trial protocols, trial execution, and some interaction with regulatory authorities e.g. scientific advice, IND or NDA submissions. In addition you preferably have experience from early stage clinical development work within the pharmaceutical industry.

You are a reliable, open-minded and dedicated team player who is effective at working within a global team environment. Interaction with internal and external experts require proficiency in English, high communication, coordination and planning capacities, as well as flexibility and a keen sense of quality. You may expect global travelling activity.

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 Richard Aranda +1 609 786 4430 (UTC - 05.00 Eastern time US & Can.).

Deadline
28 June 2013.

International Medical Specialist

• Research & Development, Medical Doctor
• Denmark - Søborg

Do you want to make a difference taking on a key role as medical specialist responsible for clinical trial medical input within our growing and maturing inflammation portfolio? The Medical & Science, Inflammation & Growth Hormone (GH) department at Novo Nordisk A/S, is seeking a physician to take on a position as global Medical Specialist to focus on the new focus area for Novo Nordisk within inflammation/autoimmunity. We offer an exciting position for professional and scientific growth with the opportunity to contribute to the development of innovative therapies. The job will require strong interaction with highly engaged colleagues and external stakeholders including therapeutic experts.

About the department
Inflammation is the newest therapeutic area for Novo Nordisk. Novo Nordisk aspires to improve the lives of people with autoimmune and chronic inflammatory diseases by developing compounds with new modes of action for rheumatoid arthritis, lupus, inflammatory bowel disease and psoriatic arthritis. Medical & Science, Inflammation & Growth Hormone consists of 14 employees and we continue to grow as the pipeline matures. Together with the other specialists areas working with clinical development for inflammation we are located in Søborg, Denmark, and Princeton, USA. We have overall global medical responsibility for Clinical Development Plans and trials in the Inflammation and Growth Hormone area.

The job
The key responsibilities of the successful candidate will be to function as a Medical Specialist within the assigned projects. This includes being instrumental in implementing clinical development and regulatory strategies for drug candidates. The person will be involved in developing Clinical Development Plans, executing and reporting clinical studies phase 1-3 trials, providing medical and clinical expertise to the generation of Product Business Plans and Strategic Product Plans as well as medical deliverables to the paediatric investigational plans for development projects. Leadership of a cross functional medical science team will also be an important component of the role. Close interaction with health authorities will be an integrated part of the job. The position will be based in Søborg, Denmark.

Qualifications
You have a medical degree including scientific knowledge and some clinical experience relevant to the inflammation area. It will be an advantage if you have previous experience from the pharmaceutical industry including experience in developing trial protocols, trial execution, and some interaction with regulatory authorities e.g. scientific advice, IND or NDA submissions. In addition you preferably have experience from early stage clinical development work within the pharmaceutical industry.

You are a reliable, open-minded and dedicated team player who is effective at working within a global team environment. Interaction with internal and external experts require proficiency in English, high communication, coordination and planning capacities, as well as flexibility and a keen sense of quality. You may expect global travelling activity.

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 Richard Aranda +1 609 786 4430 (UTC - 05.00 Eastern time US & Can.)

Deadline
28 June 2013.

Internship in Process 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 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: August 2013

Contact
For further information, please contact Nis Chræmmer Jørgensen +45 3079 1417.

Deadline
10 June 2013.

Internship in FeF Chemicals A/S

• Student and Internships
• 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 master students who bring new ways of thinking to our company.

About the department
FeF Chemicals is seeking an engaged student for a full-time internship in a project team responsible for replacing the current affiliate Quality Document Management System with the corporate Novo Nordisk Quality Document Management System in a period of 6 months commencing primo August 2013. FeF Chemicals is an organisation with close to 140 employees located in Koege developing, producing and delivering chemical raw materials and APIs to Novo Nordisk and other customers worldwide.

The job
You will be working in a dynamic project team and during your internship you will be involved in a variety of different project assignments. These will include individual as well as team and management assignments. The individual assignments includes transferring existing quality documents into the corporate Novo Nordisk document templates, translating selected quality documents into English and establishing new internal web sites. The team assignments will cover workshops concerning rewriting existing quality documents into a new LeanSOP structure and training of users in the new IT systems which beside the Document Management System also include a Document Distribution and a Document Training System. In addition you will be involved in Project Management activities. Organisationally you will be associated to our HR department.

Qualifications
You are studying for a Master´s degree in Pharmacy, Engineering or any other relevant degree. Only candidates who have not yet finalised their degree will be considered for the internship.

You have solid interest in Quality Systems, IT, Internal Communication and you are willing to be challenged both professionally and personally. You also like being part of a professional team and you have a high energy level, show initiative (proactive thinking), independence and self-motivation. Furthermore you pay attention to details and possess good communication skills in writing as well as interpersonal.

Excellent language skills in English and Danish and good computer skills with MS office are required. Experience with intra web site administration is an advantage but not a requirement.

You will get a unique knowledge of both structure and use of the Quality Management System of a modern world leading pharmaceutical company. You will be trained in all the quality systems including our intra web publishing site and you will gain unique hands-on project management experience in a professional and dynamic environment, working for and with highly engaged colleges.

Contact
For further information, please contact Eva Kjer Hansen on +45 3068 4360.

Deadline
10 June 2013.

Global Product Manager

• Marketing
• Denmark - Søborg

Novo Nordisk is preparing to enter a new exciting therapeutic area with liraglutide 3 mg, which is an investigational treatment in phase III development for people with obesity.

The department
You get the opportunity to join an expanding and high performing team of marketing colleagues in Søborg, Denmark. You will report to the Director of Obesity Marketing, and work closely with the Project Lead for Strategic Communications. You will have cross functional interactions with multiple stakeholders in HQ and affiliates, including Global Marketing and Medical Affairs, Medical and Science, Regulatory, Legal, Corporate Communications, and Public Affairs. You can expect 40-60 travel days per year.

The job
You will be responsible for projects to verify and communicate the medical unmet needs for treatment of people with obesity. Your primary task will be to develop and drive a market survey to understand the needs for new pharmacological treatment options in obesity as well as develop plans and tactics to improve medical care for people with obesity. This includes project management working closely with internal and external stakeholders to ensure timely execution at high quality. You will also drive development and execution of communication and publication plans relating to the projects.

Qualifications
To successfully master the job you have international experience from the pharmaceutical industry along with experience in planning and execution of major projects. You have a business or scientific degree, and minimum 3-5 years experience from a pharmaceutical marketing function at global or national level is required. 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.

In Novo Nordisk 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 contact Chip Amrein on +45 3075 4831.

Deadline
1 June 2013.

Senior Regulatory Professional

• Regulatory Affairs
• Denmark - Søborg

Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk medicine 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?

About the department
The RA Degludec Clinical Department is situated in the Novo Nordisk project house together with other regulatory functions in Søborg. We are group of 10 highly skilled and dedicated people involved in finalizing the global registration of Tresiba® and Ryzodeg® as well as activities related to Life Cycle Management.

Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring rapid regulatory approval in all our markets. Regulatory Affairs is a fast-changing field, and the dedicated employees in our unit need both keen negotiating skills and scientific insight to serve as Novo Nordisk’s advocates around the world and make a meaningful difference to our business.

We are currently looking for a Senior Regulatory Professional with a science background combined with regulatory experience to join our team responsible for the worldwide approval and maintenance of Tresiba® and Ryzodeg®.

In collaboration with experienced regulatory professionals and associates you will be responsible for clinical aspects of regulatory affairs activities within the projects.

The job
Responsible for planning, coordination and executing the regulatory tasks as required in the projects or existing products in accordance with the regulatory strategy for the defines area of responsibility. Responsible for preparation and compilation of the individual sections of all files for the defined area of responsibility, in accordance with internal requirements and external regulatory guidelines and regulations

In Regulatory Affairs, you’ll work in a fast-paced environment where no two days are alike. Tight deadlines, cross-departmental collaboration, project management and the challenges of international communication will be part of your busy workday. You’ll be expected to make an impact and challenge the status quo if that’s what it takes.

You will be a member of a global regulatory team and also work closely with other departments to achieve the ambitious goals of the project.

You will be involved in the planning of and responsible for preparation and maintenance of regulatory documents, the regulatory review of protocols and reports as well as working on worldwide submissions and the following interactions with health authorities. You will also be responsible for keeping up to date with current internal requirements and external guidelines and legislation within area of responsibility. Life cycle management activities will also be a part of the job.

The position has for the right person good development opportunities. Novo Nordisk offers a world of support with first rate professional training, relevant support groups and talented, friendly colleagues.

Qualifications
We expect you to have a university degree in life sciences and documented professional experience working with regulatory affairs and/or the pharma industry. Project management experience is a plus, but not required. You are organised, a good planner and a proactive problem-solver, and you’re a skilled communicator who is comfortable speaking and writing in English.

As a person, you thrive in busy environments and bring a can-do spirit and a healthy sense of humour to your work even when the pressure’s on. You’re a strong team player, but you also enjoy working independently.

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.

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 Jane Møll Pedersen at +45 3075 3759 or Dorrit Espersen +45 3075 8242.

Deadline
9 June 2013.

Team Leader

• Research & Development
• Denmark - Måløv

This is your chance to join the world leader in diabetes care and put your personal mark on R&D projects with the powerful potential to lift the quality of life for millions of people around the world. Novo Nordisk has started its voyage towards the development of solid dosage forms of diabetes proteins and peptides for oral delivery.

About the department
The job is located in Novo Nordisk, Diabetes Research Unit, Department Oral Formulation Research. We are 10 scientists and 10 laboratory technicians organised in two teams. Our ambition is to develop break-through products with orally available versions of insulin and GLP-1. You will be involved in research activities from the exploratory phase until transfer to Development.

The Job
You will be the focal point for your team. Coaching and motivating a team – as a leader and an expert in formulation of oral dosage forms – you will drive the work forward and ensure that your team meet the set goals. Your area of responsibility covers the challenges related to the creation of new oral delivery concepts, formulation activities, stability studies, capsule and coating technology. In the position, you will use your thorough knowledge of formulation of oral dosage forms as you guide your team of competent professionals. You will also engage in the scientific work in the team.

Qualifications
You are an experienced manager, able to coach and motivate a team, and you have already proven excellent leadership skills. You hold a PhD in Pharmacy, Engineering or another relevant scientific discipline and have at least 5 years of work experience within a scientific field. Additionally, you have thorough knowledge of early R&D, formulation activities of oral dosage forms. On a personal level, you thrive in a flexible and dynamic environment and are ready to embrace changes. You are assertive and able to handle several tasks simultaneously. With your superb communication and people skills, you enjoy collaborating with people from different professional backgrounds. As you will work in an international organisation, you will need very good English skills – both written and spoken.

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 Anne-Mette Lilleøre at +45 3079 0559.

Deadline
30 June 2013.

Principal Research Scientist

• Research & Development
• Denmark - Måløv

Can you develop a new oral drug delivery system for insulin and GLP-1 and thereby contribute to sustaining Novo Nordisk’s leading position in diabetes care? Then seize this opportunity to join Novo Nordisk R&D, the Diabetes Research Unit, where focus is on improved treatments for diabetes and its complications. In the Oral Formulation Research department in Måløv, Denmark, 25 committed colleagues are waiting for you to be a part of our international department and great working atmosphere.

Development of new oral drug delivery systems
As Principal Research Scientist within oral protein delivery and formulation your main objective will be to focus on the oral absorption and formulation of therapeutic proteins and polypeptides such as insulin and GLP 1. You design and develop brand new oral drug delivery systems. Moreover, you will be involved in the formulation of the drug delivery systems such as small scale preparation of tablets, encapsulation, GI-targeting, etc. You will work closely together with Pharmacology, Analysis and other R&D teams within the Diabetes Research Unit. This job will offer you a job with a high level of independence and flexibility.

Pharmaceutical background at PhD level
You must hold a relevant PhD, e.g. in Pharmaceutical Technology, and you have obtained profound knowledge of oral formulation and oral drug delivery. You must possess significant knowledge about oral drug delivery technologies and deep insight in the GI-tract physiology as well as relevant animal models for oral drug delivery. It is essential that you have an excellent track record of original research within oral drug delivery. It will be an advantage if you have experience with patents or from an R&D setting and/or specific knowledge of oral delivery of oral proteins and polypeptides combined with pharmaceutical formulation experience.

You have a flexible mindset which is helpful in the ever changing project environment. In order to make your ideas practical, you must possess a certain amount of innovation and creativity and be able to think and act unconventionally. As you will work in an international organisation, you will need good network and interaction abilities and very good English skills both written and spoken.

In Novo Nordisk 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 contact Betty Lomstein Pedersen at +45 3079 4256.

Deadline
30 June 2013.

Safety Surveillance Adviser

• Research & Development, Medical Doctor
• Denmark - Gentofte

Are you a rheumatologist or an expert in drug safety within the area of autoimmune and chronic inflammatory diseases? If yes, you may be our new colleague in Safety Surveillance Biopharm. We are seeking an experienced colleague, who is prepared to play a key role in patient safety.

About the department
We are an international team of 6 medical doctors/scientists. Safety Surveillance Biopharm has the global responsibility for the ongoing evaluation and management of the safety profile for products belonging to the product portfolio in development for autoimmune and chronic inflammatory diseases, as well as marketed products such as Growth Hormone therapy, Hormone Replacement Therapy in postmenopausal women and oral anti-diabetic treatment.

The job
Your key responsibility resides within the product portfolio in clinical development for autoimmune and chronic inflammatory diseases. This includes evaluation and management of safety data, signal detection, periodic safety update reporting, development of patient safety information and risk management activities.

You will resume the role as chairperson for a product specific cross functional safety committee, which is the authority within Novo Nordisk responsible for providing integrated assessments of safety data and endorsing appropriate actions for the product in question.

Cross-functional collaboration, in particular with global development and regulatory affairs, in a multicultural, international environment will be part of your workday.

You will work in a fast-paced environment reflecting the increasing demands from regulatory authorities while always bearing patient safety in mind.

Qualifications
You have a medical degree or equally relevant science degree topped with solid experience in one or more of the following disciplines: drug safety, pharmacovigilance, clinical development or pharmaco-epidemiology. Clinical or drug safety experience within the field of rheumatology, autoimmune or chronic inflammatory diseases is an advantage.

You are enthusiastic, energetic, confident and a strong team player. Evidently, you have a good sense of urgency and are able to cope well under pressure still maintaining a good sense of humour. You have demonstrated planning as well as analytical skills.

You are fluent in both written and spoken English, experienced user of the Microsoft Office package and possess strong communication and presentation skills.

In Novo Nordisk 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 contact Birgitte Scharling at +45 3075 5292 or Hanne Rasmussen at +45 3079 7450.

Deadline
11 June 2013.

Senior Chemist, Data Analyst

• Production
• Denmark - Kalundborg

In Novo Nordisk we strive to create added value for our patients. Every 10 seconds two persons are being diagnosed with diabetes and nearly 366 million people around the World needs our products. The aim of working for Novo Nordisk is not just putting food on the table, but to make a difference.

About the department
You will be a part of Business Support with 10 colleagues, who are responsible for the provision of various support to all of Insulin Manufacturing I (IM1) in Kalundborg.

The facility produces rapid acting insulin analogues and consists of five departments – Fermentation/Recovery, Purification, Laboratory, Support and Management within the same facility.

The job
We are offering a position, where you will be a part of a busy and stimulating environment with lots of opportunities to develop both your professional and personal competencies.

You will be responsible for providing data support to the production, including data mining from data sources, data analysis, as well as presenting data in the support of planning and creating the right basis for management decisions.

You will be responsible for ensuring compliance according to cGMP, current pharmacopoeia and ISO standards, and as a chemist you will ensure the high quality of data mining and data analysis.

Furthermore you will pro-actively seek cooperation with colleagues throughout all of IM1 to ensure that your competences are used in the optimum manner for the benefit of IM1.

Qualifications
You have an academic degree (e.g. cand. scient., cand. pharm., engineer or other equivalent level of education). You have a quality mind-set and has experience with several data sources and process control systems, e.g.: MS SQL, PI Process book™, SattLine® and Oracle®.

Furthermore you have a proven track record of obtaining new knowledge and to put it into use in the creation of useful solution for your customers, preferably using tools from LEAN and Six Sigma.

You possess a good communication skill and will be able to present complex data analysis for managers as well as colleagues.

As a person you take initiative to find and implement solutions to problems based on what you observe and on customer feedback. You work in a structured and systematic way and are used to deliver according to targets.

At Novo Nordisk it is your skills, motivation and ambitions that help us providing care for many patients that depend on us. In return we offer the opportunity to work with talented colleagues and we offer an environment where you can grow both professionally and personally.

Contact
For further information, please contact Jesper Kragh Nielsen on +45 3079 5575.

Deadline
11 June 2013.

Supporter

• Production
• Denmark - Gentofte

Do you want to join a team that supports the packaging process of NovoSeven®? At the moment we are looking for a dedicated supporter for Biopharm Finished Products Gentofte.

About the department
Our team plays a vital role in ensuring product quality and patient safety for the benefit patients worldwide.

The packaging department is the last production step before the products are shipped to customers worldwide, and we operate with a tight schedule to ensure timely delivery. Our mission for the future is clear. We want to be an excellent supplier. You will play a key role in achieving this ambitious goal and have the opportunity to grow professionally. You will be based in Gentofte, Denmark.

The job
You will be working in an involving and challenging environment. Here you will join forces with 10 dedicated and highly professional team players who support the production of NovoSeven®. You will drive the implementation of new processes and production methods, and secure compliance with GMP. Your daily tasks will include handling of customer complaints and non-conformities. Together with colleagues inside and outside the department, you will perform systematic troubleshooting in order to find root causes and countermeasures. Moreover, you will provide training to employees in the production, e.g. in relation to batch documentation, inspection methods and other quality-related issues. Finally, you will help qualify the equipment and write GMP documents.

Qualifications
You have a relevant scientific degree. Besides, it will be an advantage if you have experience from the pharmaceutical industry, e.g. in relation to qualifying equipment, cLEAN® or as a Process Supporter. Most importantly, you have a strong quality mind-set, a good technical understanding and the necessary drive to follow up and execute your tasks in a timely manner. Furthermore, you adapt easily to a changing environment where priorities shift. You have a well-structured approach to your tasks and are capable of maintaining an overview - although working under strong pressure. You possess a high level of responsibility, flexibility, independence and personal drive, just as you are able to undertake complex tasks and easily communicate issues to relevant stakeholders. You have a good sense of humour, and you speak and write Danish and English fluently.

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

Contact
For further information, please call Lone Krogh on +45 3075 8471.

Deadline
29 May 2013.

Research Scientist/Principal Scientist

• Research & Development
• Denmark - Måløv

In this job you will join a group of dedicated scientists working with preformulation and formulation of peptides and proteins

About the department
The Diabetes Research Unit is committed to the development of new pharmaceutical peptides and proteins to improve quality of life and treatment for diabetic patients. Our subunit is involved in elucidation of structural properties, biophysical behaviour and formulation aspects of peptides and proteins with the aim to develop safe, efficacious, and convenient formulations for subcutaneous delivery. In the department of Diabetes formulation situated in Måløv 9 researchers and 14 technicians employ state of the art technologies to support several research projects from idea concept and optimization to the stage of development lead selection prior to first human dose. Researchers and technicians work closely together with other units in the Diabetes research organisation in a highly inspiring and challenging cross organisational environment. Our ambition is to continuously deliver the best technical solutions to ensure success and speed of our project pipeline.

The Job
As part of the department of Diabetes Formulation your job is to drive research, preformulation and early development of pharmaceutical formulations of proteins/peptides with focus on characterization and analysis of chemical and physical stability. You will be involved in wide-ranging research projects where you are expected to take competent and reliable leadership of the formulation development process. This process requires an extensive collaboration with colleagues in the department as well as across the organisation and communication with colleagues with expertise in other scientific disciplines.

Qualifications
You have a Ph.D. degree in pharmaceutical sciences/chemistry/biophysics, and a minimum of 2-5 years of postdoctoral experience, and a proven record of experience within aspects of protein/peptide formulations. On a personal level you possess excellent communication and interaction skills and value and enjoy the collaboration with experts in related fields of expertise working in cross organisational project groups towards a common goal. You have a thorough understanding of where your effort creates value to projects.

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 Helle Birk Olsen at +45 3079 6299 or Svend Ludvigsen at +45 3079 6169.

Deadline
14 June 2013

Team Leader CSP Process Support

• Production, Team Leader
• Denmark - Måløv

The Novo Nordisk R&D pipeline continues to grow, which means that we have a lot of challenging tasks in Clinical Supplies Packaging, securing a continuous improvement of quality, efficiency and lead time.Do you want the responsibility for managing these challenges and at the same time work with developing and managing people.

About the department
In Clinical Supplies Packaging you will be joining 55 colleagues, divided into 3 teams (Packaging, Process Support and Shipping), who have the responsibility for packaging and distribution of trial supplies for clinical trials, conducted at more than 1000 sites worldwide. CSP works in close collaboration with the rest of the clinical supply chain in CMC to achieve the overall goal of timely supply of medicine for the Novo Nordisk clinical trials – an important milestone in quick and efficient development of new drugs.

The Job
As team leader in Process Support, you will be responsible for supporting the processes of packaging and distributing drug supplies for the clinical trials in Novo Nordisk.You will be leading a team of 13 dedicated employees (warehouse operators, technicians, chemists, project coordinators, and a business analyst) with plans of additional ramp up, in order to support the increased activities in the coming years.Your team is overall responsible for ensuring that the processes are in compliance with GMP and GDP. This responsibility covers supporting the packaging and the distribution process throughreview of documentation, handling quality concerns/non conformities, warehouse management and IT support, and improving quality levels through process optimisation and standardisation. Furthermore the team is responsible for ensuring equipment and facility validation and readiness for production and inspection and establishing and maintaining procedures, as well as continuously evaluating automisation levels and possibilities as well as ensuring sufficient storage capacity and capability in the department to match the changing requirements.

You will be an active part of daily operation board meetings, systematic problem solving and setting the direction for the team. You work closely with the team leaders from own department and the rest of the clinical supply chain, securing an end to end mindset and a holistic approach to solving the complex task of delivering products to Clinical Trials.We offer a challenging job with exiting future development opportunities and the possibility to impact the department by setting a clear direction for your team.

Qualifications
You either have an academic degree within a relevant field of expertise or have a solid working experience within operations management and especially production/packaging in a GMP environment. You have at least 2 years management experience preferably managing in a team setting. You have a proven ability to inspire and motivate others and to empower your team members to deliver high quality results. You are well-organised, results driven and responsible. You base your analysis on facts and you approach challenges in a logical manner and find practical solutions. You have the ability to prioritise and plan ahead, while keeping focus.

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 Malene Gundestrup at +45 3075 9703.

Deadline
7 June 2013

Deadline

Development Scientist for raw materials

• Research & Development
• Denmark - Gentofte

In this position, we offer a unique possibility to create and shape your own job. An emerging field of focus opens a position as development scientist with focus on the use and introduction of new raw materials into our development processes.

About the department
The department is part of CMC API Development, R&D, and is responsible for developing and transferring scalable purification processes for proteins in order to bring the growing pipeline of new therapeutic proteins into clinical trials. An increasingly important part of this task is ensuring that we have the right raw materials from the right manufacturers.

The working climate in the department is informal with emphasis on a scientific approach to our work and a high degree of flexibility. The work is performed in multidisciplinary project groups closely allied with Research, Analytical, Formulation, Production and Quality departments. Thus, a wide interdisciplinary understanding of the development process for biopharmaceuticals is needed to support decision making and progress within this area.

The Job
The major task is to manage the introduction of new raw materials into our biopharm development portfolio. This consists of evaluating the suitability of the materials, including quality, virus safety and manufacturing conditions. You will have the responsibility of ensuring progress in the whole value chain from manufacturers via sourcing and QA to the final use of the materials in our clinical productions. In addition to managing the incoming materials, you will also be involved in defining and implementing new routines and processes of handling raw materials for the whole area.

Your job will also include participation in the general development tasks of the department. This includes development and evaluation of virus removal in downstream processes, writing regulatory documentation for our clinical trials with respect to virus removal, and virus safety of raw materials. Coordinating and managing smaller projects may also be part of your responsibilities.

We offer a position in which you will be able to develop your knowledge of drug development with all its interdependencies and regulatory challenges. You will contribute to interdisciplinary project teams and have the opportunity to develop your scientific, project management or line management skills.

Qualifications
You should hold a scientific academic degree in engineering, biology, chemistry, or another relevant discipline. Preferably, you have experience within the field of protein drug process development, virus safety evaluation or raw materials handling. You are enthusiastic, open-minded and flexible by nature; you thrive on challenges and are able to work both independently and in a team environment.

In Novo Nordisk 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 contact Camilla Kornbeck at +45 3075 1270.

Deadline
7 June 2013.

Medical Advisor

• Medical
• Denmark - Greater Copenhagen area

In this job, we offer an exciting career with lots of challenges, personal and professional development among good colleagues in a positive working environment.

About the department
The job is located in Novo Nordisk Danish affiliate based in Copenhagen. As Medical Advisor you will be part of a team of three dedicated Medical Advisors with focus on diabetes medical affairs strategic and field operations in Denmark.

The Job
Reporting directly to the Clinical Medical and Regulatory Director DK & NO, the Medical Advisor will drive medical activities within the territory such as local meetings with specialists, general practitioners and hospital departments. The Medical Advisor is expected to provide medical input for the development of medico-marketing strategy, sign-off on promotional material, deliver internal and external medical information and education. The role will involve liaison with Key Opinion Leaders and investigators.

Qualifications
To be considered for the role you must have a medical degree, preferably with clinical experience within endocrinology. You have a proactive mind-set and a strong can-do attitude, and you are able to work independently.This position requires scientific expertise, strategic thinking, resource management skills, and preferably Good Clinical Practice experience. You must be fluent in Danish, hold a valid driver’s licence and be willing to travel within the territory most working days. Approximately 25 days of international travel per year should also be expected.

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 Ralf W. Ackermann at +45 3075 3297 or Josefin af Petersens at +46 706 38 89 46.

Deadline
31 May 2013

Chemists for Process Support

• Production
• Denmark - Kalundborg

We are looking for 2 experienced Chemists – one within environmental monitoring and one within formulation. If you are an ambitious person with a positive can-do approach, then you will fit just right in…

About the department
You will join 183 colleagues in AP Filling & Supply at Novo Nordisk’s Site Kalundborg, which counts a total of 3.500 employees. We are responsible for the formulation and filling of insulin for Novo Nordisk’s packing department.

job
As Chemist within formulation you will handle non-conformities and OOS results from the laboratories. As Chemist within environmental monitoring you secure environmental compliance and handle non-conformities, e.g. within aseptic behaviour and environmental monitoring. Both of you will drive several processes and smaller projects and contribute to all areas of the aseptic production. You will achieve success by entering into close collaboration with the Operators and your colleagues in the production. You will also make an effort to understand the processes and build good relationships to colleagues in functions such as QA, QC, packaging, RA, suppliers. Look forward to a strong LEAN culture where we focus on improving our work processes to enable us to work even smarter and more cost-consciously. As such, you will have plenty of possibility for developing your personal and professional skills.

Qualifications
Either you have a natural sciences’ degree or you have shown that you can take on vast responsibility and a structured approach to developing and using knowledge. In any case, you have several years’ experience with GMP from the pharmaceutical or a similar industry. You know how to handle quality-related documentation such as SOPs, deviations, validation, change requests, analysis results and media filling. In your previous jobs you have had variable workloads and proven your ability to prioritise and maintain your high level of motivation. You thrive in a team-oriented culture, and you have trained your ability to drive processes and smaller projects efficiently. Lastly, you are motivated for a job in which you receive thorough training in a multitude of different aspects of an aseptic production.

At Novo Nordisk, you will join a patient-centred culture of talented professionals. We respect individuality and empower you to make the most of your potential.

Novo Nordisk in Kalundborg

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. We are at the front edge of the development within technology, systems, methods and processes. If you are our new colleague, we can guarantee opportunities that you will have a hard time finding anywhere else.

Contact
For further information, please call Thorid Lassen on+45 3075 8009.

Deadline
2 June 2013.

Production planner

• Production
• Denmark - Hillerød

Would you like to join a team of highly skilled employees in a position with great influence and responsibility, and help ensure that our patients receive their insulin on time? Join us and become Production planner for Site Denmark Logistics in Novo Nordisk, Product Supply.

About the department
Product Supply is an organisation with close to 10,000 employees located in Denmark and at one of our 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 located in Kalundborg, Bagsværd and Hillerød, and this position is based in Hillerød.

Site Denmark Logistics is responsible for the long and short term planning, coordination and prioritisation of activities within the Novo Nordisk’s production of diabetes products. The purpose of the department is to support a stable and ambitious supply chain organisation, by working closely with production. A focus on performance and a proactive communication with our customers is essential to ensure a coordinated, prioritised and finely executed delivery. On a daily basis we interact with a large network of stakeholders within Novo Nordisk including production, launch coordination and sales offices from all over the world. We are focused on getting our products “fast to market” both in regards to a stable flow in our existing production and when launching new products, and LEAN is an integrated natural part of the way we operate.

The job
You will be working in a challenging and highly dynamic logistics team with nine dedicated employees. We are responsible for ensuring aligned and well balanced production plans of FlexPen® and FlexTouch® in close collaboration with the production, our customers and other stake holders. You will represent the costumer’s voice in the production sites and prioritise timely production and release of orders. Furthermore we are performance orientated and this will require constant focus on our KPI’s (Key performance indicators). You will be responsible for securing production capacity for the forecasted orders by updating supply/demand scenarios on a monthly basis. Use of various IT system including SAP, PRISM, LIMO will be an extensive part of your job.

Qualifications
You are passionate about logistics and production planning and you hold a Master´s or Bachelor’s degree in Production Engineering, Logistics, Supply Chain management or relevant degree. Documented working experience within logistics and production is an advantage, however, not a prerequisite, and we welcome applications from new graduates. You are fluent in written and spoken English since our corporate language is English, and you have flair for IT.

Besides this you thrive on working in a fast-paced environment. You are positive, independent, energetic and flexible. You see solutions instead of problems and you take initiative. You are a team player and are able to handle numerous tasks simultaneously.

At Site Denmark DFP, 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 on+45 3075 6719.

Deadline
9 June 2013.

IT Governance Analyst

• IT
• Denmark - Bagsværd

Are you interested in working with global implementation of IT processes? Do you want to be an important partner in establishing and developing a global process support function? Do you like to work with continuous improvements of IT processes? Then join IT Process Office, a group of 6 enthusiastic experts within process management and quality system management.

About the department
The IT Process Office is part of the IT Governance unit in Novo Nordisk. Our main stakeholders are IT management groups and IT personnel in the global IT organisation. The group manages global IT processes, conducts IT Risk management reporting, IT audit and inspection coordination as well as training management.

The job
As IT Governance Analyst you interact with our stakeholders at all levels of the organisation. You advice and train your colleagues in the global IT organisation and work closely with process owners in maintaining and improving processes.

Your key challenges will be to contribute to the global implementation of IT processes and to the establishment and development of the global process support function in IT Process Office. You conduct continuous improvements and from time to time you take on the project manager role of strategic initiatives.

You will be responsible for one or more processes within IT, and you will act as the central subject matter expert in this area. The global IT processes have process managers and owners as well as other stakeholders around the global IT organisation and you will be responsible for supporting and helping them in assessing the process performance as well as assessing possible impact of proposed changes to processes.

You thrive in an international business environment, are comfortable with complex challenges and ambitious goals, and can stand up to the pressure that comes with taking on significant global responsibilities.

Qualifications
You have a Master’s degree within computer science, engineering or economics. You could come from a similar position, but you can also have a background as project manager, IT consultant, IT analyst, business analyst or test manager having at least 5 years’ experience. Preferably you have practical experience working with ITIL, COBIT or other international frameworks. Your IT development or implementation experience enables you to assess risks and impacts of proposed changes to global IT processes and to have qualified dialogue with stakeholders around the IT organisation. You possess strong cooperation skills and can influence your surroundings in a positive way. You have extensive experience as presenter and you can communicate effectively across cultures and functions. You are capable of working independently, taking on responsibility and show initiative.

Also, it is vital that you have effective time management skills and enjoy handling multiple tasks simultaneously without compromising the quality. You are fluent both in written and spoken English. Previous exposure to a pharmaceutical or similar regulated IT environment is an advantage but not a pre-requisite.

The job is based in the greater Copenhagen area (Bagsværd), but some travel activities must be expected.

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 Bo Vindberg on + 45 3079 4923.

Deadline
7 June 2013.

Process Development Specialist

• Research & Development
• Denmark - Søborg

Are you interested in working with clinical data management processes, training and competency development in a global environment? Do you want to be an important partner in the drug development process? Do you like to work with cutting edge knowledge and processes? Do you like a challenging and rewarding workplace?

About the department
Then join the Data Management (DM) Anchor’s group of 9 enthusiastic experts within clinical data management, data management processes and standards, and quality and ressource management. The DM Anchor is responsible for supporting data management and developing and maintaining state-of-the-art data management processes globally. We are seeking a new colleague to take up a position as Process Development Specialist, working to support and strengthen our global DM organization.

The job
You will work with our headquarter DM organization, our global Clinical Data Management (CDM) units, our customers in Trial Management, Biostatistics and other data operations personnel within clinical development, and with our outsourcing partners. The Process Development Specialist is primarily responsible for optimizing business processes and organization, providing expert support and training on DM processes within and outside DM, participate in audits and facilitate and drive improvement initiatives and knowledge sharing.

Qualifications
You have a degree in the life sciences, pharmaceutical science, statistical science or a similar field. Additionally, you have experience and/or education within information management such as computer science or programming. You are knowledgeable and experienced in the area of international clinical data management and planning and conducting DM deliverables. You have thorough knowledge of GCP and you have documented experience from working in GCP/ISO environment. You have extensive experience as a presenter and you communicate effectively in cross-cultural situations. Furthermore, good English skills and strong cooperation are a necessity. You are capable of working independently, taking on responsibility and show initiative. We expect you to be able to oversee several tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast.

In Novo Nordisk 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 Jon Pauls +45 3079 9010.

Deadline
16 June 2013.

Associate Sourcing Professional

• Supply Chain and Logistics
• Denmark - Bagsværd

The Purchasing department, part of Novo Nordisk’s central Supply Chain Management organization, is looking for an Associate Sourcing Professional for the Filing and Tableting team, for a one year maternity leave replacement.

About the department
The office is situated in Bagsværd.We are a team of 13 dedicated colleagues, and are responsible for setting up and maintaining effective supply chains for sourcing of production materials. We ensure the supply of these materials to all Novo Nordisk Filing and Tableting production and development departments worldwide. Your main responsibility will be inventory and order management of the Process Aids category, including both daily operations and improvement projects.We are looking for a highly motivated and result oriented candidate, who takes pride in delivering high quality work, on time and in a pro-active way.

The Job
Our ambition is to deliver high quality services to manufacturing sites and their production departments.You will be responsible for specific items, and will ensure deliveries to production in full and on time. To achieve this, you will be in direct contact with our production sites and suppliers, you will monitor inventory level of your items, prioritise needs from production and coordinate activities with other functions in Sourcing Operations to secure availability of released material, and you will place purchase orders with international suppliers and follow up on deliveries to NN warehouses.Additionally, you will participate in or drive improvement projects related to process you’re a part of.

Qualifications
We expect you to have a higher education (preferably Master’s Degree) within a relevant discipline e.g. Supply Chain Management, Engineering, or alike, with 0-2 years of purchasing or supply chain experience. Excellent data management skills, an analytical mindset and an ability to work independently with Excel and SAP will be assets. And finally, you are fluent in English and Danish.

As a person you have a high energy, a positive mindset and are open towards other people and new ideas. You work independently and you like a dynamic environment with many simultaneous tasks and changing priorities, while managing strict deadlines. You thrive in international environments, with people of diverse backgrounds.You master English fluently, both written and spoken.We offer you an exciting job among great colleagues and in a positive working environment, potentially providing a platform for other positions in the department or Novo Nordisk.

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 Maud Le Crom at +45 3075 6476.

Deadline
26 May 2013

Chemist

• Research & Development
• Denmark - Bagsværd

Development Scientist of microbial fermentation processes.Are you a dedicated scientist highly skilled in developing, characterising and optimising microbial fermentation processes? Then you could be our new colleague in The Diabetes Upstream Development team.

About the department
Our team is a part of the department Diabetes Upstream and Downstream Development, located in Bagsværd. The department is responsible for development of the upstream process steps, fermentation and initial recovery, as well as downstream process steps as precipitation and purification of drug substances for toxicological and clinical trials. The department that is anchored in the CMC Supply area in Research and Development.

The Job
You will: Plan, execute, evaluate and report experimental work in the laboratory, carried out both independently and in collaboration with team members.Support pilot and production facilities during production of material for clinical trials.Participate actively in the development and testing of new process technology and in the establishment of technology standards in fermentation and recovery, based on your relevant experience and knowledge.Take an active part in further building our knowledge and skills in both microbial cultivation and initial recovery processes.We expect you:To be motivated by challenges and that you have a “can-do” attitude.That you are able to work independently and have the ability to look for opportunities instead of limitations.To participate actively in the project group as well as in the cross organisational project work.

Qualifications
You:Hold a PhD or master degree as chemical engineer, pharmacist, cand. scient. or similar.Have some years of practical experience with developing yeast and/or e-coli fermentation processes.We expect that you:Have knowledge and hands-on experience in working with bioreactors (batch, fed batch and continuous culture).Have experience with initial recovery processes such as centrifugation, homogenisation, refolding and filtration processes.In addition to this, commitment to science and its industrial application, excellent communication skills, positive attitude and being a team player is expected from you.

We offer:A dynamic ever changing, always collaborate and humorous environment with the best colleagues on the northern hemisphere.We are involved through most phases of a development project, from the selection of recombinant cell candidates in collaboration with Discovery to upscale and transfer of processes to pilot and production facilities.

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
If you would like to know more about the position, please contact Ann-Louise Hansen at +45 3079 9646 or Mogens C. Jensen phone at +45 3075 6004.

Deadline
5 June 2013

Internship in Device R&D

• 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, primarily within diabetes care. The main focus is to develop novel and innovative injection systems for self treatment. Device Research & Development has a long and outstanding track-record of developing the best, most innovative and widely-used injection systems in the world.

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 international and 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 a change 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 CAD 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 judgment 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 an opportunity to be become part of this in 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 4-6 months.

Start date: 12 August 2013.

Contact
For further information, please contact Lars Bom +45 3075 1324.

Deadline
10 June 2013

Senior International Trial Manager

• Research & Development, Trial Manager
• Denmark - Søborg

Do you want to be part of a dynamic team that drives the trial activities through a fast track development path within our fast acting insulin portfolio.

About the department
Clinical Operations, Insulin & Devices-2 in Global Development is looking for an experienced colleague to join us in a position as Senior International Trial Manager. We have a team of enthusiastic International Trial Managers, Data Managers and Clinical Trial Administrators who are responsible for planning and conducting clinical trials within the Insulin and Device area.

The Job
Your key function will be to drive the progress of a large and complex phase 3a trial within our fast acting insulin portfolio. Your main responsibilities will be to plan, coordinate and manage global clinical trial activities from the preparation of study protocols to reporting.You will chair the trial related international study group, for which you will plan and conduct team meetings that maximise information sharing and stakeholder engagement. You will cooperate closely with Novo Nordisk affiliates worldwide as well as all other partners involved in the daily management of our clinical trials. You will have special focus on supporting daily insulin bolus titration surveillance. You will participate in, and contribute to relevant Investigator and Monitor meetings.The job requires that you apply a structured and analytical approach during the development of relevant trial documents, including recruitment strategies, communication plans and trial budgets.

Qualifications
You have a relevant educational background, preferably a university degree in Natural Science or equivalent with a minimum of 5 years of experience in trial management related positions. You speak and write English fluently, and have a broad knowledge of clinical trial methodology and experience from working in a project organisation.Our ideal candidate has a strong quality mind-set, communicates effectively and with high impact, meets deadlines, is well structured and able to work with multiple and frequently changing priorities in a dynamic environment. You are a dedicated team player, can inspire and motivate, and have a high degree of cross-cultural awareness.

You will be part of a successful, expanding company in which working is not just a way to make a living, but a way to make a difference.

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 Kirsten Bang Thøfner at +45 3079 6242.

Deadline
28 May 2013

Project Manager

• Finance
• Denmark - Bagsværd

Novo Nordisk is one of the world’s most successful pharmaceutical companies and has a great growth potential. If you are motivated by the opportunity to be part of this success, consider applying. And if you are interested and preferably experienced in SAP FI/CO and accounting and have a proven record for understanding complex business processes end-to-end and delivering optimal SAP solutions, you may be the person we seek.

About the department
Accounting Processes is part of CAS (Corporate Accounting Services), a department in Corporate Finance at Novo Nordisk. The department’s primary responsibility is to ensure development of our SAP FI/CO system and accounting processes to identify and implement optimal solutions together with our IT organisation. SAP is a strategic priority in Novo Nordisk and we are working on a portfolio of activities and projects that will leverage the usage of SAP across Novo Nordisk.

The Job
You will be part of a dynamic team of accounting and SAP specialists responsible for delivering high-quality financial and IT solutions – you will also have the opportunity to develop a broad spectrum of finance and IT skills, and to gain extensive knowledge of the business.You will be responsible for driving projects with focus on structuring and optimising accounting processes, and further utilisation of SAP functionality. Most projects involve international reach and change management, as well as close contact to other finance units throughout our organisation. In addition, our accounting knowledge and experience are used to handle the accounting for a number of affiliates and to develop the data processing handled by our company in India. We expect you to be an active part in the continuous development of the high level of accounting, SAP and project management expertise in the department and in Novo Nordisk.We invest in professional and personal development, and have a thorough individualised development plan for each employee. Through on-the-job training, projects and courses, you will experience a continued steep learning curve and gain valuable knowledge.

Qualifications
We expect that you have a bachelor’s or master’s degree in Accounting, Finance or similar. You have a solid experience with SAP FI/CO. Ideally, you have 2-4 years of experience with project management. Furthermore, you have strong analytical skills and an engaging personality showing strong responsibility for your tasks and projects. Combined with your strong communication skills and good sense of humour, these traits allow you to contribute proactively to our team with ideas and initiatives. In addition to being fluent in written and spoken English, you should also be a proficient user of IT tools and ready to invest both time and effort in your personal and professional development.

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 Bente Askholm, at +45 3079 6933.

Deadline
31 May 2013

Project Manager

• Sourcing
• Denmark - Bagsværd

Do you have a strategic mind-set coupled with a strong personal drive and solid project management skills? Are you motivated by driving change and supporting strategic procurement projects in an international environment with multiple stakeholders? Do you have ambitions for pursuing a career in Novo Nordisk and further develop skills within procurement and project management–then you are the person we are looking for.

About the department
Corporate Procurement is, in close cooperation with international affiliates and stakeholders, responsible for the sourcing and purchasing of the global indirect spend in Novo Nordisk. Corporate Procurement has more than 100 employees and is a part of Corporate Finance. You will be part of a newly established department responsible for driving the Global Category Management Programme, which is a key strategic initiative in Corporate Procurement. The main objective is to support the establishment of globally aligned category strategies across key indirect spend categories. This entails close cooperation with multiple stakeholders from all areas of the organisation including international sourcing units, Marketing, Finance, R&D, IT etc.

The Job
As a Project Manager you will take part in the continued development of the Global Category Management Programme. You will be working closely with the Category Managers to design and execute on the establishment of global category strategies that challenge the status quo, takes the category to the next level, and delivers value to the organisation. The Category Managers are responsible for the categories and together you will analyse global spend patterns, manage and align with internal stakeholders globally, develop procurement levers and propose a governance setup for the on-going category management. Key to success will be your ability to quickly grasp the category and through a structured approach to problem solving conclude on essentials and prepare clear and effective communication to the global organization. The category strategies are subject to approval by key stakeholders including senior management representatives.

Qualifications
The person we are looking for has completed a relevant Master's Degree (e.g. economics, business administration or supply chain management) with an excellent result. Ideally, you have been working several years as a Consultant, Project Manager or Category Manager with experience in managing multiple stakeholders in an international environment. Sourcing experience is not a prerequisite – but a keen interest in developing within this field is essential.As a person, you have a high drive and persistence. You are a team player and enjoy working and sparring with colleagues to reach optimal results. Through your previous assignments you have developed excellent project and change management skills. You possess strong analytical skills and an ability to prepare clear and concise presentations.In Novo Nordisk it is your skills, commitment and ambitions that help us improve the lives of millions of people across the world. In return we offer you the opportunity to work with talented colleagues in a dynamic, international environment, and a wide range of opportunities for professional and personal development.

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 Rune Tradsborg Pedersen on +45 3075 7685.

Deadline
3 June 2013.

Head of Clinical Outsourcing Management

• Research & Development
• Denmark - Søborg

Would you like to set the direction for clinical outsourcing in the world’s leading diabetes care company? We are looking for a manager to drive and develop our global clinical outsourcing activities in alignment with the growth and needs of our business.

About the department
You will be heading up a department of 10 experienced clinical outsourcing managers who interacts closely with our development projects providing outsourcing support when agreements with external parties are entered. The department is further responsible for managing the global clinical outsourcing process and system within the Global Development organisation, ensuring supplier/risk management and driving the strategic direction of the clinical outsourcing area.

The Job
As head of Clinical Outsourcing Management you will be responsible for day to day management of our dedicated outsourcing team providing leadership, direction and prioritisation for the unit. You must ensure management and development of the global clinical outsourcing set-up including adequate coverage of quality and ethics perspective’s in the sourcing processes.Further you will be responsible for developing and realising our sourcing category strategies, secure tight management of preferred suppliers and focus on managing risks related to clinical sourcing. Thus, you will on a continuous basis interact with key vendors and key internal stakeholders.You will be member of the GD Clinical Services management team holding responsibilities for clinical process optimisation and health economics beyond sourcing. As part of the management team, you will contribute to the continued development of the area and in securing cross functional as well as global collaboration. We expect you to take part in developing GD Clinical Services as an inspiring and challenging place to work.

Qualifications
You have a Master degree in pharmaceutical/biological science or economics and experience with clinical development from the pharmaceutical or health care sector. You have a proven track record as a line manager and possess a thorough interest for the business perspective. You are strong in positioning your case and hold a commercial and analytical mind-set, good negotiation skills and an excellent command of written and spoken English.You provide leadership by setting clear direction and taking the lead yourself in realising it. You have focus on motivating the team and know how to benefit from diverse competencies. You are a team player but also able to take and stand by clear decisions. Your work style is proactive and you are motivated by taking on new and challenging tasks.

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 Jesper Nyegaard Nissen, at +45 3079 7768.

Deadline
30 May 2013

Internship in Customer Insights.

• 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 have the opportunity to join an international, high performing team responsible for generating customer insight (being physicians and patients) and utilise the insight 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 Project Managers in the Customer Insight team in day to day market research project management. In this role you will support project vendor selection, project planning, questionnaire review, logistic project management and final project reporting and summarisation. You will also be involved in tasks of analysing market dynamics, and customer insight alongside Global Project Managers and Global Product Managers, providing input of customer insight 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 economics, marketing or other relevant fields and have demonstrated strong project management and analytical skills through your study. General knowledge about market research and pharmaceutical industry is preferred. We expect the candidate to be goal oriented, thrive in a busy environment and bring a can-do attitude. Fluency in both oral and written English and excellent interpersonal skills are required.

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.

Practicalities

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: 01.08.2013

Contact
For further information, please call Wei Sun on+45 3079 7855. or Michael Hemmann on+45 3075 2726.

Internships for Biopharm Business Support

• 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 master students who bring new ways of thinking to our company.

About the department
Biopharmaceuticals (Biopharm) is an organisational unit in Novo Nordisk Product Supply and we are responsible for the manufacturing of a range of products across multiple geographical locations. We are currently seeking a number of interns for our Business Support area which is responsible for logistics and planning of raw material purchasing, management of Biopharm economy, EHS and IT, facilitation of the overall Biopharm business strategy, and driving of launches and strategic projects.

The job
In accordance with your background and interests you will be part of either Biopharm Strategies, Logistics, IT or Environmental Health & Safety (EHS). In the relevant section you will work together with our managers and project managers and take part in various projects and tasks related to one of the above areas.

You will assist on or solely run daily tasks, conduct analyses, report updates and perform ad-hoc tasks. These assignments will give you hands-on experience with a wide range of tasks and processes of real value to Novo Nordisk and insights into important projects. You will be considered an integrated member of the relevant department and you will receive continuous feedback on your work.

Qualifications
We expect you to have a good understanding of business processes. You are currently studying for your master's degree, e.g. within business, marketing or supply chain management. Only students who have not yet graduated will be considered for the position.

You are an outgoing person with a strong personal drive and dedication. You are service minded, thrive in a busy environment and bring a can-do attitude. We also expect you to possess good communication skills in both oral and written Danish and English and experience with Microsoft Office.

Practicalities

Start date: August/September 2013

Contact
For further information, please Jonas Bremer on +45 3075 7222.

Deadline
10 June 2013.

Internship in IT Project Execution, 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
As an intern you will be part of IT Project Execution, a competency centre that includes several specialised IT departments. IT Project Execution is part of an inspiring community of around 300 skilled and dedicated IT professionals who are responsible for all major IT projects and IT systems at Novo Nordisk. You will have ample opportunity for professional sparring and best practice exchanges in your daily work. The intern position is based in Bagsværd, Denmark.

The job
In IT Project Execution we want to develop our competencies and the way we conduct our training in a more efficient way. You will support the PE Management team in revisiting the current competence development and training set-up the IT Project Execution organisation. In this role you will perform targeted literature searches to address strategic questions on how to organise competence development and training, and help to develop a concept for training of the various roles in the IT organisation going from Project Manager, IT Specialist to Department Managers. Together with the management team, you will be key driver in developing a concept for how training and competence development can be organised going forward, and the subsequent implementation hereof. As part of this workshops, communication with key stakeholders, analysis of the current training set-up and job profiles, etc. will be parts of your daily tasks.

Qualifications
We are looking for an intern who is passionate about competence development, training and learning methodologies. You are currently studying on your master’s degree in cand.merc., cand.merc.HRM. or other relevant field. General knowledge of competence development, learning practices, training approaches and key methodologies (organisational analysis, literature reviews, business cases and research) is preferred. The ideal candidate has a “can-do” attitude and is excellent in translating theoretic concepts into concrete plans and actions that suit the specific training need. You have excellent communication skills and a genuine desire to collaborate across boundaries. You have a well-structured approach to your tasks, take responsibility, and you are eager to contribute to the continuous development of the area of training and competence development in the global IT Project Execution organisation. You have a high level of independence and pro-activity as well as a quality mind-set. You are fluent in English, both written and orally, and you have excellent computer skills. 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: 15 August 2013

Contact
For further information, please contact Malene Jørgensen +45 3079 6002 or Hayriye Gjøderum +45 3079 6008.

Deadline
10 June 2013.

VP Enviromental Coordinator

• Environmental, Health & Safety (EHS)
• Denmark - Gentofte

Do you take a burning interest in external environment issues and can you drive this agenda across business units? Then you could be our new environmental VP coordinator.

We are looking for an ambitious and highly skilled professional to take up the position as environmental VP coordinator for the two VP areas Biopharm Aseptic Production (BioAP) and Biopharm Tablets & Finished Products (BioT&FP), in Biopharmaceuticals.

About the department
Your new work location will be BioAP Technical Service in Gentofte, where we supply utilities to production and pilot departments and laboratories in Gentofte and Værløse. The supply of utilities consists of a.o. WFI, clean steam and gasouses with related analyses and execution of projects. We are 45 employees divided into 4 teams with close relations to production, QC, QA, consultants and suppliers.

You will be a part of the EHS coordinator network in Biopharm.

The job
You will be responsible for ensuring that BioAP and BioT&FP meet Biopharms and Novo Nordisk’s environmental policies and targets, and maintain the ISO 14001 certificates. More specifically, you will be responsible for target setting, KPI reporting and ensuring compliance with Danish legislation and environmental approvals. You will corporate with Novo Nordisk’s External Environment Department on compliance issues.

Also you will be an anchor person during environmental audits and follow up on non-conformities, ideas for optimization and action plans.

You will head a group of local environmental stewards and energy responsibles, and take part in coordination of the work with other Environmental and Health & Safety VP coordinators in Biopharm, to maintain an effective network between the VP areas.

Qualifications
You hold a relevant Master degree, or equivalent skills, with strong results from years of successful work in either Line of Business or Corporate Functions within the environmental area.

You have analytical skills and like working with numbers, along with a structured approach to problem solving and good communication skills, combined with humour. Project coordination skills will be an advantage.

Access to own car is needed. Danish in speaking and writing is a prerequisite.

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 Kirsten Haarder on +45 3079 9183 or Allan Kjeldal on +45 3075 9280.

Deadline
3 June 2013.

Team Leader

• Research & Development
• Denmark - Måløv

Do you want responsibility for developing and managing people and optimizing work processes in a rapidly growing part of Novo Nordisk’s R&D organisation? Then we have a job for you.

About the department
CMC Clinical Supplies Labelling and IT (CSLIT) is responsible for a range of services supporting our clinical trials world-wide. Our clinical trial activity will be high in the coming years and to support this development, we are seeking a new team leader. Today, we are 45 engaged colleagues.

CSLIT occupies a central and cross-cutting role in the research projects. Therefore an important part of your role will be to ensure optimal collaboration with a number of internal and external partners in Denmark and abroad. This includes all our affiliates involved in Clinical trials, as well as suppliers of printed materials, labels etc.

You will report to the CSLIT Director and be a member of the department management team, which consists of 6 colleagues besides you. You will be located at Novo Nordisk’s site in Måløv.

The job
As team leader you will manage a team of 17 Labelling and Graphics co-ordinators, who are dedicated to design labels, booklets and directions for use for clinical research projects. All these are designed in-house, and some are printed in-house whilst others are printed by suppliers.

You will lead your team towards the achievement of challenging goals and timelines. Given the current high level in clinical trial activity, one key focus is on improvement of processes, reduction of lead time and increase of productivity. Therefore, you must be able to create and support a value set that drives a LEAN culture where continuous improvement is a natural part of everyday work.

You will be responsible for setting and meeting the team’s operational goals e.g. timely delivery of labels by ensuring effective allocation of people and resources to the various clinical trials. You thrive in working both with operational daily management as well as setting long term direction. You will act as sparring partner to your team - coaching and empowering team members to deliver timely and sound business results, and you will take an active and dedicated role in their own professional and personal development. As a member of the CSLIT management team, you will contribute actively in developing department strategies and targets, and in supporting a good working climate.

Your responsibility is to follow up on performance, focus on continuous improvement of processes, development of employees and last but not least the well-being of your team.

We offer you the opportunity to work in Novo Nordisk’s R&D organisation which is the largest R&D organisation in Denmark. We promise you constant challenge and the opportunity to be part of a dedicated and enthusiastic department as well as a dynamic management team. You will develop your managerial skills, work with many internal and external contacts internationally, and you will develop your personal competences and skills.

Qualifications
You have proven leadership and people management experience, preferably from line management. You have a proven ability to inspire and motivate others and to empower your team members to deliver high quality results. Experience from the pharmaceutical industry and/or GMP production and clinical trials will be a further asset. You are goal oriented and through your strong analytical skills you can identify, plan and overview many parallel business processes and prioritize the most value adding initiatives and ensure their implementation. Your personal leadership style is characterised by accountability, integrity and personal engagement.

You have an academic background.

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 Peter Christensen on+45 3079 2774 or Anne Mette Gam Kristensen on+45 3075 7150.

Deadline
5 june 2013.

Strategy Project Director

• Business Support
• Denmark - Bagsværd

Corporate Strategy is part of Corporate Development and responsible for the overall corporate strategic planning process for Novo Nordisk, executing ad hoc strategy projects for Executive Management including considerations with regards to strategic partnerships and acquisitions as well as managing Novo Nordisk’s portfolio of equity investments.

About the department
As our new Strategy Project Director you will join the Corporate Strategy team, which consists of five dedicated employees located in Bagsværd.

The job
In your role as Strategy Project Director, you will be responsible for analysing, structuring, coordinating and executing projects of significant importance to Novo Nordisk. This will include responsibility for the considerations related to strategic partnerships as well as merger, acquisitions and divestment opportunities, where you will be responsible for the key work streams liaising with key stakeholders across the organisation to ensure a holistic strategic solution.

Furthermore, you will have responsibility for executing the equity investment strategy including board representation on behalf of Novo Nordisk at several biotech companies as well as handling new potential equity investments.

As you will work broadly within the organisation and with senior management interaction, you should be able to and feel comfortable working with all levels within the organisation. You will be able to gain a broad business understanding enabling a number of career opportunities in a global perspective and personal development is an important and integrated part of a global career in Corporate Development.

Qualifications
You have a solid scientific background combined with several years of industry relevant experience in working with strategy processes preferably with a background as a consultant or from a biotech or pharmaceutical company. This has provided you with keen analytical, strategic and financial skills and ability to, based on the scientific understanding, interact with relevant key stakeholders and establish a holistic strategic solution.

You will be working closely with colleagues across the organisation and across geographies, so strong communication, collaboration and relation building skills are critical qualifications. You thrive in a busy environment, bring a can-do attitude, and you maintain a healthy sense of humour, also when the pressure is high. You are a team player, but also enjoy working independently. Finally, you master the English language both in speech and writing and are willing to invest time and effort in personal and professional development.

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 René Holmen Pedersen at +45 3075 6546.

Deadline
31 May 2013

Event Adjudication Adviser

• Quality
• Denmark - Bagsværd

Are you interested in clinical trials and pharmacovigilance? – Then we have the right job for you.

About the department
We are looking for 4 Event Adjudication Advisers to join the event adjudication adviser group from 1st of August 2013. The event adjudication group consists of 12 highly engaged colleagues from various academic backgrounds; who work in a fast-paced environment reflecting the increasing demands from numerous long term clinical trials and regulatory authority requirements. In an increasing number of trials, certain clinical adverse events are required to be adjudicated. Event adjudication is a process where an independent review board of medical specialists assesses the relevant events for fulfilment of pre-defined clinical criteria.We belong to Safety Operations, one of the functional areas in Global Safety. Global Safety is responsible for the global handling and reporting of adverse events to authorities, and the surveillance of the safety and quality of Novo Nordisk clinical development and marketed products. The department is situated in the House of Quality in Bagsværd.

The Job
As an event adjudication adviser you will be responsible for coordinating, driving and interacting with stakeholders across Novo Nordisk and being the link to international external service providers. Project management, process setup, on-going event tracking, documentation review, and creating and communicating reports are examples of what this dynamic role comprises of. The role varies according to the life of a clinical trial with regard to pace and task type. Some of these tasks are data and database driven. We are a rapidly growing department with a high focus on continuous improvement, so optimization tasks will also be part of the job.

Qualifications
You have a Bachelor or Master degree, preferably within biomedical sciences (e.g. Medicine, Pharmacy, Veterinary) or related discipline. You speak and write English fluently. Experience in pharmacovigilance, event adjudication would be an advantage but not a must. You have a flair for IT systems and are highly skilled in MS office, specifically Excel. You are good at communicating, planning and coordinating multiple activities. You have excellent cooperative skills and a high degree of flexibility. As a person you are dynamic, eager to learn new processes, careful with your tasks and have a positive attitude to challenges. You must be able to work against tight deadlines.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 Poonam Rihel, at +45 3079 1131 or Claudia Pierleoni-Nielsen, at +45 3075 9671.

Deadline
2 June 2013

Quality Consultant

• Research & Development
• Denmark - Hillerød

Can you enhance the understanding of our Quality Management System across an R&D organisation counting 300 employees? If so, this is your opportunity to become our new consultant and advisor. You will get the chance to take on a leading role in Device R&D and put your mark on processes and our way of working in an organisation where all our actions need to be world-class.

About the department
You will join a dedicated team of 5 LEAN & Quality Experts, located in Hillerød. We are responsible for cross-functional process improvements in Device R&D. Our focus is LEAN leadership, project planning, project risk management and QMS. Device R&D designs and develops delivery systems that enable people with chronic conditions to live their lives as they wish to. We are world leading within development of diabetes injection devices.

The job
Your overall objective is to strengthen our strategic focus within QMS, and as our new expert within this field you can look forward to having full support from the management team. A vital part of your success will depend on your ability to enhance the understanding of QMS across the Device R&D organisation’s app. 300 employees – and your ability to find easy-to-understand-and-work-with solutions in close collaboration with a great variety of managers and other stakeholders in Novo Nordisk.

You will be responsible for projects related to improvements of QMS as well as the implementation and maintenance of these. This could be e.g. projects on compliance and inspection readiness or updating of instructions and/or templates for deliverables within product development. You must challenge and align the quality improvement activities anchored in our quality activity plans. You are also responsible for coordinating Device R&D input to procedures and instructions, and you will represent Device R&D in Novo Nordisk QMS groups.

Qualifications
You have an MSc in Engineering and a minimum of 3 years’ relevant experience working with quality and change management processes within a pharmaceutical and/or medical technical company or in a consulting group. Therefore you have a sound understanding of our basic workflow and processes, and you have the overview and structured mind-set it takes to challenge and improve these. Using your positive and outgoing personality and your stamina you can take personal responsibility for your tasks and turn these into successes. To you, major challenges only make the job more fun, and you will need all of your strong communication and interpersonal skills to meet these challenges.

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 Lotte Juul Foghsgaard on +45 3075 6518.

Deadline
3 June 2013.

Internship in External Environment

• 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
Novo Nordisk is seeking an engaged student for full time internship to Product Supply Global Support organisation in a period of 6 month. Novo Nordisk Product Supply is an organisation with close to 10,000 employees located in Denmark or at one of our 5 international sites. Product Supply is responsible for all production in Novo Nordisk and delivery of products to our sales affiliates or directly to major customers.

Challenges

You will be working in a department called “External Environment”. The department manage environment, health and safety issues within Novo Nordisk.

The job
During your internship your key task will be internal webpage- GlobeShare project, which includes operating internal web page for the department and functional teams. Also you will be involved in designing and preparing material for External Environment newsletter roll-out.

Qualifications
You like being part of a professional team. You have a high energy level, initiative (proactive thinking), independence and self-motivation.

You pay attention to details and possess good communication skills both in writing as well as interpersonal.

You are studying International Business Communication, Business Language and Culture, Business Administration, Engineering or any other relevant degree. You have solid interest for internal communication, IT, and willing to be challenged both professionally and personally.

Excellent language skills in English and Danish are a requirement, and good computer skills with MS office. Experience with Front Page or another web site tool is an advantage but not a requirement.

You will gain unique hands-on project management experience in an international and dynamic environment and a paid internship. You will also be trained in GlobeShare publishing site.

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 September 2013

Contact
For further information, please call Sarah Ørtoft on +45 3075 7761.

Deadline
10 June 2013.

Editor

• Communication & Public Affairs
• Denmark - Bagsværd

Are you a journalist who is ready to start a new career managing the news flow in a major global corporation? Or perhaps you are a journalist who has made the jump to a corporate environment and are now ready to bring your skills to a new level?

If you can answer 'yes!' to either of the above, then a new position in Corporate Communications might be for you.

About the department
Novo Nordisk is not the world's biggest pharmaceutical company, but we do a lot of good things that most other companies don't. One of the missions of Corporate Communications is to find those stories, and tell the world about them. We do this via a variety of channels - some aimed at employees (an online news site, employee magazine and quarterly CEO video), and some aimed at the external world (press releases, the corporate website, and corporate Facebook, Twitter and YouTube accounts.)

Corporate Communications consists of 45 people working with internal mass media (which we call Employee Communications), media relations, leadership communication and film.

The job
Our new editor will be a part of the Employee Communications team, and will work closely with Media Relations, as well as other colleagues in our department and around the world.

His or her tasks will include identifying compelling, strategic stories; prioritising and scheduling them for the appropriate channels; and producing much of this content, either by writing it yourself, editing others' copy, or hiring freelancers.

Our science-driven company is full of wonderful stories. However, the pharma industry is highly regulated and very complex. So in addition to being a great journalist, our new editor must also be flexible and a good listener - sensitive to concerns from sources and colleagues, and able to compromise when needed.

Qualifications
Minimum 5 years' experience writing, editing and publishing news for print and web. Experience working with internal communication in large global organisations is a plus. Excellent written and spoken English is required; Danish skills are a plus. Experience with multimedia publishing (video, radio, social media), and a talent for numbers and statistics are a plus.

Strong interpersonal skills are key. Days can be long when a story or deadline demands it, so you must be flexible re working hours. Some travel is required.

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 Gwendolyn Carleton on +45 3079 4309.

Deadline
31 May 2013.

Internship Project assistant

• 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 get the opportunity to join the Records Management department where we currently drive a Quality programme consisting of business and IT projects. Records Management processes are continually and rapidly changing as new external requirements have to be implemented and Novo Nordisk expands its global reach. As project assistant, you will help implementing new records management processes to meet the changing demands.

The job
You will support the project managers within the programme with different project management activities. In this role you will take part in the organisational change management activities to ensure that the organisation is prepared for the changes and the project is implemented in a smooth and successful way. You will also assist in preparing and follow up on activities related to steering committee and project meetings and assist in workshop planning, execution and follow up.

Qualifications
We envision an intern who is passionate about working in a project environment and maybe is seeking a career as a project manager. You are currently studying on your master’s degree in health economics, economics, IT or other relevant field. General knowledge of the project management disciplines is preferred. Knowledge within records and document management and IT will be an advantage.

Meetings and presentations in English will be part of your daily work, so good communication skills and fluent English are required. The candidate is preferably living in an European country and we expect that candidates can work independently but also be part of a team and who is able to handle several tasks at the same time.

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 positive can-do attitude 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: 5 August 2013.

Contact
For further information, please call Stine Adrian Møller on +45 3075 3028.

Deadline
10 June 2013.

Project Assistant

• Production
• Denmark - Hjørring

Do you want an administrative job in a multi-cultural team and help Novo Nordisk change lives? Then please read on and apply for the position as Project Assistant in Novo Nordisk Needle Manufacturing Sourcing in Hjørring.

About the department
You will be part of Needle Manufacturing Development and have 20 dedicated and professional colleagues. We work dedicatedly with the establishing and qualification of the necessary production equipment, capacity extensions and improvements as well as life cycle management projects in connection with manufacturing and development of Novo Nordisk’s needles.

The Job
You will be responsible for optimising and improving the administrative processes within the department. Joining the department’s management team, you will work closely with the Department Manager and the project teams. This means that you will prepare documents, reports and documentation, and in this way support the project teams. In addition, you will have a wide range of administrative assignments such as arranging department meetings and seminars, drafting of related minutes, just as you will follow up on the plans of action. Moreover, you will have a coordinating role in the training of your colleagues and be the administrative key employee in charge of purchases, filing activities etc.

Qualifications
You have experience from administrative processes and projects, preferably in internationally oriented companies. You have a flair for IT, are a solid user of Microsoft Office programmes and proficient in written and spoken English. You make an effort to be visible and have an outgoing personality. Additionally, you maintain your positive and service-minded attitude – even when many busy colleagues need your assistance at the same time. No need to mention that you possess a true and unfailing service mindset as well as excellent multitasking skills.

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 Kim Lindblad Carlsen at +45 3075 5850.

Deadline
27 May 2013

International Medical Director/International Medical Manager

• Research & Development, Medical Doctor
• Denmark - Søborg

The Medical & Science, Degludec II department at Novo Nordisk A/S is seeking a physician to take on a position as International Medical Director/Manager working with diabetes projects in Novo Nordisk. We are looking for a medical doctor with documented clinical and scientific knowledge about diabetes. A candidate with experience from clinical development work within the pharmaceutical industry and knowledge about interaction with regulatory agencies will be preferred. The job will require strong interaction with highly engaged colleague’s world-wide and external stakeholders including treating physicians and therapeutic experts.

About the department
The department is medically responsible for planning and conducting clinical studies as well as medical input to regulatory documents and health authority interactions. The candidate will be involved in these activities closely interacting and collaborating with the NN organization globally.

The Job
Key responsibilities of the successful candidate will be to take up the role as Medical Specialist within the assigned projects. This includes being instrumental in creating regulatory documents, implement clinical development strategies for a drug candidate, updating Clinical Development Plans, executing clinical studies phases 1-3 and providing medical deliverables to the paediatric investigational plans for a drug candidate.

A specific focus will be to provide input to the content and quality of the regulatory documents, Clinical Part of the Submission Dossier as well as creating / writing relevant risk-assessment plans, medical content of trial outlines, protocols, clinical trial reports, paediatric investigation plans, IMPDs and publications and presentation of medical aspects of the clinical development program at internal and external meetings (including meetings with health authorities, congresses, investigator meetings etc.).

Qualifications
You have a medical degree including scientific training (PhD, DMSc or equivalent), and preferable knowledge within diabetes or metabolic conditions. It will be an advantage if you have previous experience from the pharmaceutical industry and experience from interaction with regulatory authorities e.g. NDA submissions, scientific advice or similar. You are a reliable, open-minded and dedicated team player, who thrives in a global environment of continuous development, and focuses on completion, quality and results. Interaction with internal and external experts require proficiency in English, high communication, coordination and planning capacities, as well as flexibility and a keen sense of quality. You may expect certain travelling activity of approximately 10%.

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 Pernille Poulsen on +45 3075 9214.

Deadline
31 May 2013.

Safety Surveillance Specialist

• Quality
• Denmark - Bagsværd

Are you a medical doctor who is passionate about patient safety? Then you may be one of our new safety surveillance specialists.

We are seeking medical doctors (MD) with documented clinical and scientific knowledge about diabetes, metabolic conditions or cardiology for two (2) full time positions as Safety Surveillance Specialist in Safety Surveillance Diabetes Insulin & Devices department of Global Safety, in Novo Nordisk A/S.

Drug safety is an integral part of drug development and is now in focus more than ever. In this job, millions of people with diabetes worldwide depend on your medical evaluation of the benefit/risk profile of the Novo Nordisk insulin products.

About the department
Safety Surveillance Diabetes Insulin & Devices is an international department of highly committed and skilled professionals with medical or pharmaceutical background. We have the global responsibility for the safety surveillance of the Novo Nordisk insulin products and devices, marketed or in clinical development.

The job
Your key responsibility will be the ongoing safety surveillance of insulin products. This includes evaluation of the safety data, early detection of safety signals and aggregate reporting hereof, as required by the EU and US legislation. Close collaboration and communication with other functional areas in Novo Nordisk, especially the clinical development team and regulatory affairs team is required.

Your job responsibilities will also include communication with external parties related to clinical safety monitoring, such as Data Monitoring Committees and Event Adjudication Committees.

Qualifications
You have a medical degree (MD) and preferable also scientific training (PhD or equivalent). It will be an advantage if you have previous experience from the pharmaceutical industry, especially from a medical department or a drug safety department. Experience from interactions with regulatory authorities will be a plus. You are a reliable, open-minded and dedicated team player, who thrives in a global environment of continuous development, and focuses on quality of work and the results of the team. Interaction with internal and external experts require proficiency in English, excellent communication, coordination and planning skills.

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.

Applications must be written in English.

Contact
For further information, please contact Liliana Hansen at +45 3075 0964.

Deadline
10 June 2013.

Environmental Management Partner

• Environmental, Health & Safety (EHS)
• Denmark - Søborg

Do you want to impact the environmental agenda of a world-leader in the healthcare industry? Then please read on as we are looking for a new colleague that wants to work with EHS Management according to ISO14001/OHSAS18001.

About the department
You will join 23 highly skilled colleagues in the department, External Environment, situated in Søborg. Here we focus our efforts on supporting the Novo Nordisk organisation in environmental, health and safety (EHS) matters to deliver on the objectives of the corporate environmental strategy. In Novo Nordisk we have decoupled our environmental impact from financial growth and we manage our business in accordance with the Triple Bottom Line where financial responsibility, environmental responsibility and social responsibility are taken into consideration.

The job
You will play an important role in setting direction and develop Novo Nordisk’ EHS Management System according to ISO14001 and OHSAS18001. Your main responsibility will be the environmental area (ISO14001), where you will ensure continuous improvements in the system, relevant EHS tools and training of the organisation. Moreover, you will drive the EHS Steering Group, with EHS representatives from each of the ISO14001 certified areas of Novo Nordisk. You will also contribute to fulfilling External Environment’ own EHS targets, support the EHS organisation in EHS challenges and drive projects related to EHS Management. The job includes a high degree of stakeholder management on all organisational levels and collaboration across a large organisation with highly complex EHS issues.

Qualifications
You have topped your relevant Master’s degree with minimum 5 years’ experience with Environmental Management preferable from a production environment. Besides this you are a skilled project manager capable of developing and implementing projects within a global organisation with multiple stakeholders. As such, you rely on an involving and proactive style to engage your stakeholders disregarding the organisational level. This also calls for strong communication skills and a sound business understanding. You have a systematic approach to your work enabling you to attend to details without losing sight of overall targets. Additionally, you are capable of performing both individually and as a part of a team, and you have proficiency in written and spoken English.

At Novo Nordisk, you can look forward to change. We encourage our employees to make the most of their talent. And we reward hard work and dedication with the opportunity for continuous learning and personal development.

Contact
For further information, please contact Sif Press-Kristensen at +45 3079 4509 or Tomas Schou-Winter at +45 3075 1458.

Deadline
27 May 2013

Senior International Trial Manager

• Research & Development, Trial Manager
• Denmark - Søborg

Do you have extensive experience in driving global clinical trials and do you want to exert your influence by managing large global trials in rheumatoid arthritis or growth hormone disorders? Are you also prepared to embrace and tackle constant changes as part of your work each day? Then we may have just the right job for you.

About the department
Inflammation & Growth Hormone is the newest therapeutic area in Novo Nordisk. In Clinical Operations, Inflammation & Growth Hormone, we are now approx. 40 employees and we continue to grow as the pipeline matures. We are characterised by a world-class team spirit and quality mind-set, by our change readiness and an open, trust-based and creative working environment. We are responsible for the planning and implementation of clinical trial activities in accordance with the Clinical Development Plans in Inflammation and Growth Hormone, including trials in Rheumatoid Arthritis (RA), Crohn’s Disease (CD), Systemic Lupus Erythematous (SLE) and Growth Hormone Deficiency disorders. We collaborate internationally with other R&D units, with CROs and to a growing extent, with our Novo Nordisk affiliates.

The job
The job as Senior International Trial Manager demands that you are capable of directing and driving large global phase 2b/3 trials. You will be responsible for ensuring that project key deliverables are met in time, at a high quality and within budget. You will be a member of the international study group, for which you will plan and conduct team meetings that maximise information sharing, stakeholder engagement and decision making. This includes vendor management of CROs participating in the trial execution. You will participate in and contribute to relevant investigator and monitor meetings.

The job requires that you apply a structured and analytical approach during development of relevant trial documents such as trial protocol, informed consent, recruitment strategies, risk analysis plans, communication plans and trial budgets. You are detail-oriented, while able to maintain overview, digest complex data and evaluate the adequate level of quality.

You are expected to be able to identify better practices and create improvements and you will be able to chair cross-project/cross-functional tasks forces. You may act as trainer across projects and mentor new staff.

Qualifications
You hold an academic degree within the natural sciences or healthcare, and speak and write English fluently. You are a clear communicator and can inspire and motivate a team to deliver their best in an ever-changing environment. You have a strong knowledge of clinical trial planning and execution and a minimum of 5 years’ experience in managing large clinical trials.

You have a quality mind-set, communicate effectively and know how to prioritise between different tasks in a dynamic environment which requires a high degree of flexibility. You work independently while also being a dedicated team player. You have excellent cross-cultural awareness and like to contribute to multi-cultural project groups.

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.

You will be part of a successful, expanding company in which working is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Louise Høyer at +45 3075 1535 or David Mollerup at +45 3079 9133.

Deadline
9 June 2013.

International Trial Manager

• Research & Development, Trial Manager
• Denmark - Søborg

Do you have experience in driving global clinical trials and do you want to exert your influence in a new therapeutic area by managing large global trials in rheumatoid arthritis or growth hormone disorders? Are you also prepared to embrace and tackle constant changes as part of your work each day? Then we may have just the right job for you.

About the department
Inflammation & Growth Hormone is the newest therapeutic area in Novo Nordisk. In Clinical Operations, Inflammation & Growth Hormone, we are now approx. 40 employees and we continue to grow as the pipeline matures. We are characterised by a world-class team spirit and quality mind-set, by our change readiness and an open, trust-based and creative working environment. We are responsible for the planning and implementation of clinical trial activities in accordance with the Clinical Development Plans in Inflammation and Growth Hormone, including trials in Rheumatoid Arthritis (RA), Crohn’s Disease (CD), Systemic Lupus Erythematous (SLE) and Growth Hormone Deficiency disorders. We collaborate internationally with other R&D units, with CROs and to a growing extent, with our Novo Nordisk affiliates.

The job
As International Trial Manager you will have responsibility for the international coordination of clinical trial activities. You will be responsible for ensuring that project key deliverables are met in time, at a high quality and within budget. You will be a member of the international study group, for which you will plan and conduct team meetings that maximise information sharing, stakeholder engagement and decision making. This includes vendor management of CROs participating in the trial execution. You will participate in and contribute to relevant investigator and monitor meetings.

The job requires that you apply a structured and analytical approach during development of relevant trial documents such as trial protocol, informed consent, recruitment strategies, risk analysis plans, communication plans and trial budgets. You are detail-oriented, while able to maintain overview, digest complex data and evaluate the adequate level of quality.

Qualifications
You hold an academic degree within the natural sciences or healthcare, and speak and write English fluently. You are a clear communicator and can inspire and motivate a team to deliver their best in an ever-changing environment. You have a good knowledge of clinical trial planning and execution and a minimum of 3 years’ experience in managing large clinical trials.

You have a quality mind-set, communicate effectively and know how to prioritise between different tasks in a dynamic environment which requires a high degree of flexibility. You work independently while also being a dedicated team player. You have excellent cross-cultural awareness and like to contribute to multi-cultural project groups.

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.

You will be part of a successful, expanding company in which working is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Louise Høyer at +45 3075 1535 or David Mollerup at +45 3079 9133.

Deadline
9 June 2013.

Research Scientist

• Research & Development
• Denmark - Måløv

Yeast expression systems and proteolytic processing of peptides are among our core competencies for the production of pharmaceuticals which millions of people depend on every day. If this is the kind of challenge you are looking for please read on.

About the department
Novo Nordisk’s Department for Protein Expression has an opening for a research scientist with expert knowledge of yeast genetics, protein expression and secretion. The position includes development and optimisation of yeast expression systems for recombinant proteins of pharmaceutical relevance.

The Department for Protein Expression is part of the Novo Nordisk Diabetes Research Unit, DRU, and is located in Måløv, a suburb of Copenhagen, Denmark. Our department has a long and dedicated history within the field of recombinant protein expression, and you will be collaborating with highly motivated scientists to strengthen our expertise within the field.

The job
You will be part of a team in a highly dynamic and challenging environment within the Diabetes Research Unit. The Department for Protein Expression covers disciplines ranging from screening of expression systems and yeast strains to optimisation of continuous cultivation conditions and initial recovery operations. We work with state-of-the-art equipment and facilities.

Our department offers a stimulating and enthusiastic research environment. You will work in cross-departmental and cross-functional project teams together with colleagues with a variety of scientific backgrounds. You will contribute to several projects in which you will be responsible for developing yeast expression systems for heterologues proteins.

You will refer directly to the team leader, and your main internal contacts in your daily work will be scientist colleagues, technicians and project members, as well as managers in Novo Nordisk R&D, mainly within the Diabetes Research Unit. Developing and maintaining strong networks will be an important part of your work.

Qualifications
You have a strong background in molecular biology, biochemistry, or yeast genetics. Preferentially you have practical experience with engineering yeast hosts for heterologous protein expression and setting up screens or selections. Additional experience with biochemical characterization of proteases will be an advantage, but not a prerequisite. You hold a PhD and have experience from working in either an academic or industrial team.

You have very good communication and collaboration competences as you will be expected to collaborate effectively with colleagues within the department as well as in multidisciplinary project teams. You have experience with supervision or management of, for example, students or technicians.

You are result-oriented, innovative, have personal impact and a sense of individual responsibility. You are also open to new ideas and have good interpersonal skills.

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 Kjeld Olesen on +45 3075 2821.

Deadline
31 May 2013.

Chemist

• Production
• Denmark - Kalundborg

Do you have a drive and do you want to ensure the right quality on the analysis in Biopharm? Then you might be our new chemist in a QC laboratory where excellent performance is on top of the agenda. Become part of Biopharm QC in Kalundborg, where we support the production of the NovoSeven®.

About the department
Novo Nordisk, Biopharm QC, Ka performs chemical and biological analysis on API and API stability studies.

We are on the verge of implementing new analyses for support to Biopharm AP. To keep up with the implementation of the new analyses while supporting the present production, we are in need for another ambitious mind.

The department consists of 48 dedicated employees divided into three teams. We have a busy and stimulating environment with lots of opportunities to develop both your professional and personal competencies. We are looking for a chemist for our ELISA/ALMEN team. Today the team consists of 7 laboratory technicians, 4 chemists, 1 laboratory trainee and 1 Associate Manager.

By joining 45 enthusiastic colleagues in this department, you will have an opportunity to make a difference for people with haemophilia worldwide.

The job
As a QC chemist, your objective is to secure the daily routine of analysis results and delivering these to our stakeholders. You do fast and quality compliant problem solving, this is crucial in order to meet the production targets. You have to be able to evaluate and solve challenges based on your analytical skill on a high GMP level. It is important that you can handle several tasks at the same time and can finish them in due time. You will have the responsibility of writing different documents such as SOP’s, qualification reports, change requests etc.

LEAN is an important part of our daily work. You will be involved in systematic problem solving, optimisation and standardisation of processes to bring our products faster to market. We have a high focus on improvement of our processes both with regard to quality, costs and lead time.

In this challenging environment and to make sure that we take action, you communicate your observations and ideas to relevant managers and other stakeholders.

Qualifications
Your background is a relevant Master’s degree within the natural sciences, and as such you could be a Chemist, Chemical Engineer, Biologist or Pharmacist. On top of this, you have solid insight into GMP and ELISA/BIOASSAY processes. To achieve success in this job, you are tuned in on sharpening and acquiring new skills to become the best at what you do. You can easily picture yourself thrive in a complex organisation where processes and circumstances change, and you deal with colleagues of different backgrounds. Besides your quality-mindset, you have a winning attitude and focus on achieving your goals. You also have a positive, cooperative spirit and are known for taking action and following through on your tasks. Eventually, you master English as well as Danish.

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 Gitte Rølle on +45 3075 1495.

Deadline
27 May 2013.

QC Metrology Supporter

• Production
• Denmark - Bagsværd

Do you have experience with metrology, and can you handle a great variety of tasks from driving projects over handling incidents to writing Standard Operating Procedures? If you thrive on working with quality control, you could be our new QC Metrology Supporter.

About the department
You will join QC Packaging Materials in Bagsværd. We are responsible for quality control of printed and primary packaging materials to production departments in Denmark and abroad. Today we are 38 employees in two teams. The vacancy is in the QC Primary Pack team. Our focus is to deliver high quality adhering to agreed deadlines and budgets – every time.

The job
Your main task will be maintenance of our metrology processes and support to our QC assistants. A key area of responsibility will be to optimise and develop equipment and systems for quality control. You coordinate and are operationally responsible for projects, including validation of equipment, where you define milestones and ensure that we meet the agreed deadlines. Handling incidents and writing Standard Operating Procedures (SOP’s) are other tasks on your agenda. All in all, you can look forward to an exciting and challenging job.

Qualifications
You are newly educated with a background within the natural sciences. You have 1-2 years of experience from a GMP-regulated environment, including hands-on experience with quality control and measuring systems. In addition, you have a keen interest for and insight into calibrating and validating of IT-based quality control systems. If you do not have practical experience with LEAN already, you are eager to learn all about it. You are known to be very structured, and you can analyse an incident and pinpoint the cause – and afterwards adjust methods/procedures/processes in order to prevent the problem from recurring. As Metrology Supporter you must also thrive on having contact to many people, and you take on a proactive and curious approach to your work. To succeed, it is also vital that you can independently plan and drive your own tasks. Fluent in Danish is a prerequisite.

At Novo Nordisk, you will help some 366 million people who are living with diabetes. We expect high performance and the ambition to make your mark on our business. In exchange, we offer global opportunities for professional and personal development.

Contact
For further information, please contact Christine Sandorff on + 45 3075 7331.

Deadline
26 May 2013.

IT Lead - Manufacturing Execution Systems

• Production
• Denmark - Bagsværd

If you have a strong knowledge of Manufacturing Execution Systems and Production Processes, combined with the ability to communicate with various stakeholders from different layers in the organisation, we have just the right job waiting for you. As IT/Process lead on MES you will have the opportunity to personally impact the way we use our business critical manufacturing systems and processes across Novo Nordisk.

About the department
You will join a colleague in Diabetes Finished Products IT, which is a part of our Business Support team which is more than 30 employees. Together you will focus on strategic initiatives in order to standardise IT/automation regarding MES and related production processes in a global perspective.

The job
Your overall objective is to secure a stable and harmonised use of Manufacturing Execution Systems across Product Supply. A vital part of this will be to monitor the process performance and data quality across our Manufacturing Execution Systems and to drive behaviour changes ensuring improvements of both manufacturing processes and systems.

One of your most important tasks will be to establish and facilitate an Area Responsible Super User network and develop a plan to ensure your success in driving this network. You will also be involved in start-up phases of various projects where you contribute to ensure alignment with the standards and processes in general. Finally, you must contribute to sharing the strategy, visions and best practises in order to create and strengthen a common and proactive approach towards data correctness. You can look forward to approximately 20 travel days per year.

Qualifications
You have a relevant degree at master’s level backed by a minimum of 3 years’ experience from a job where you have gained profound knowledge within Manufacturing Execution Systems, SAP and production processes, preferably within the pharmaceutical industry. You have the ability to illustrate and communicate an overview of a complex situation, identify areas with potential for optimisations, develop and implement these – in top notch quality.

You are used to work independently and you can drive projects and systematic problem solving activities with minimal guidance. You need to have very good communication skills – in written and spoken English.

At Novo Nordisk, we have been changing diabetes since 1923. If you are ready to strengthen our position as an innovative pioneer and respected industry leader, we encourage you to join us to make the most of your talent.

Contact
For further information, please contact Thomas Zakarias at +45 3079 1039.

Deadline
27 May 2013.

Chemist

• Production
• Denmark - Hillerød

Would you like to work with production processes and ensuring quality? Then you might be our new chemist. We are searching for a chemist to support fermentation in our API production in Hillerød.

About the department
Biopharm API Mammalian Cell Production is placed in Hillerød where we are 100 colleagues. We produce Haemophilia API and the department have responsibility for product quality until delivery to our filling plant. The production process consists of cultivation of mammalian cells and a recovery process based on liquid chromatography. We are on the point of manufacturing to market. You will play a key part in helping people with Haemophilia all over the world.

The Job
In close cooperation with your colleagues in the production support team you will ensure that the cell growth process is in compliance with all regulations. As such, you will make sure that we follow up on the products and handle the documentation according to the GMP standards before releasing a product. You will spend time on the shop-floor, knowing that being close to the process and the operators will help you solving problems early and effectively. On an on-going basis, you will handle systematic problem solving and trouble shooting on deviations. Additionally, you will optimise processes in close collaboration with other support functions and the QA-functions. Depending on your skills and experience you will be involved in one or more of the parallel projects running in the department. As you will be part of production support team you will be expected from time to time to support production on problem solving also outside normal working hours. You can expect a dynamic and varied working day with an informal atmosphere.

Qualifications
You hold a degree in Engineering, Pharmacy or another discipline of the natural sciences. This is supplemented with a couple of years’ relevant experience within pharmaceutical production and preferably within cell growth. You have a strong mind-set for quality and compliance and preferable LEAN experience. As a person you can stay focused in a busy working day and you always approach tasks and colleagues with a positive attitude and energy. You are analytical and work in a structural way and are used to deliver according to deadlines. You possess good communication skills both in Danish and English.

At Novo Nordisk, your skills, dedication and ambition help us to 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 Karen Mette Krieger Lassen on+ 45 3075 3598.

Deadline
26 May 2013.

Global Compensation Analyst

• Human Resources
• Denmark - Bagsværd

Do you want to be part of supporting organisational growth through continuous optimisation of global remuneration initiatives?

Do you want to be part of ensuring a compensation and benefit structure that attracts and retains the right employees and drives differentiation in total rewards based on performance / value creation?

Do you enjoy providing data analysis that makes a solid foundation for pay decisions in Novo Nordisk?

We are looking for a new colleague in Global Rewards.

About the department
The position is located in Denmark in the area of Corporate People & Organisation. We are 12 employees in the VP area Global Rewards and Global Careers. Global Rewards is responsible for job-evaluation systems (Mercer), compensation and benefit programs and optimising the performance management process in Novo Nordisk.

The overall goal for the Global Rewards team is to continue to develop the Novo Nordisk Global Reward & Performance Management strategies in support of Novo Nordisk strategy and goals globally. We are responsible for designing and developing Rewards & Performance tools, programs and processes in support of different areas of the company. Our primary stakeholders are senior and executive management, and together with the regional Rewards and Performance Management specialists we lead strategy implementation through the HR business partners. Our department is highly respected by our stakeholders and you will interact with both senior management and HR colleagues throughout the world and across functional areas.

The job
You will be responsible for conducting various compensation analyses and reporting to both assess how Novo Nordisk is delivering on its reward strategy and as support to annual processes and projects - e.g. salary benchmark of selected key positions to ensure they paid competitively or job level assessment. In addition, you will be given responsibility for managing annual processes within compensation and/or performance management.

On a day to day basis you’ll work closely with both your colleagues in Global Rewards and with HR professionals across our business and depending on your experience you will be part of determine the go-forward model for salary benchmarking and reviews.

This position will be a unique opportunity to be part of an ambitious, dedicated and highly respected team that drive the reward agenda in Novo Nordisk. We are working truly global and you will be part of a rapidly growing organisation with many opportunities. You can set your mark on the future compensation design and capabilities. You will also be part of our Global Core rewards team.

As the role is a newly created position, you will be able to influence your tasks depending on your competencies and experience. You will report into the Vice President of Global Rewards and Global careers.

Qualifications
You have a master degree and ideally a couple of years of experience from a diverse international company. The experience can be within various areas from compensation, data analysis and financial analysis to process management. More importantly, is a genuine interest in compensation. You are data driven and proactive, and you are highly motivated by working in a team and learn from others. You enjoy working with numbers, conducting analysis and digesting data and have experience in connecting data with organisational opportunities and challenges. You have strong communication and collaboration skills and are able to build relations with colleagues. You are ambitious and strive for excellence and have a quality mindset in everything you do. Additionally, you should have strong IT and data management skills with a thorough knowledge of applications such as Excel, SAS and PowerPoint. Lastly, you master the English language – both in speech and writing.

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 Julie Birk Lauridsen on +45 3079 8729.

Deadline
30 May 2013.

Global Rewards Manager

• Human Resources
• Denmark - Bagsværd

Do you want to be part of supporting organisational growth through continuous optimisation of global remuneration initiatives?

Do you want to be part of ensuring a reward structure that attracts and retains the right employees and drives differentiation in total rewards based on performance / value creation?

Do you wish to be part of developing best practices and successfully drive performance management – individually and organisationally to ensure that we grow our business and continue to deliver competitive results?

We are looking for a new colleague in Global Rewards.

About the department
The position is located in Denmark in the area of Corporate People & Organisation. We are 12 employees in the VP area Global Rewards and Global Careers. Global Rewards is responsible for job-evaluation systems (Mercer), compensation and benefit programs and optimising the performance management process in Novo Nordisk. You will report into the Vice President of Global Rewards and Global Careers.

The overall goal for the Global Rewards team is to continue to develop the Novo Nordisk Global Reward & Performance Management strategies in support of Novo Nordisk strategy and goals globally. We are responsible for designing and developing Rewards & Performance tools, programs and processes in support of different areas of the company. Our primary stakeholders are senior and executive management, and together with the regional Rewards and Performance Management specialists we lead strategy implementation through the HR business partners. Our department is highly respected by our stakeholders and you will interact with both senior management and HR colleagues throughout the world and across functional areas.

The job
Your role is predominantly focused on providing a Total Reward support role for a part of our organisation. More specifically and depending on your experience this includes Base Pay design, Pay for Performance analysis, position evaluations, salary benchmarking for management teams, STI design and review, performance management support, LTI programs.

You will play a key role in delivering Rewards & Performance Management Programs in support of our Global Remuneration Strategy and Performance Management ambitions. Moreover, you will participate in cross functional projects within the area of Rewards – depending on your experience it could be with job architecture, performance management, further optimise governance around compensation etc.. You will work closely together with other experienced Global Rewards managers in the team as well as rewards specialists in our affiliates. You will be the driver of specific processes within the Global Rewards team and hence drive, develop and implement initiatives in the area of compensation, position evaluation and/or performance management.

This position will be a unique opportunity to be part of a team that that create a world class standard and that have great influence on the future compensation strategy. We are working truly global and you will get a unique outset to a global rapidly growing Organisation. We are in the middle of a significant transformation within the Global Rewards team to ensure that we continuously stay best in class. You will also be part of our Global Core rewards team

Qualifications
You have a master degree and several years of experience from a diverse international company within the field of compensation management. You are analytical and proactive, and you are highly motivated by working in a team and learn from others. You have a natural impact on different stakeholders and are able to engage other people through your strong communication skills. You have experience in connecting data with organisational opportunities and challenges and you are able to design a strategy and implement it also through others. You are ambitious and strive for excellence and have a quality mindset in everything you do. As you will be involved in several projects at the same time, you must be able to juggle many projects simultaneously. Additionally, you should have strong IT and data management skills with a thorough knowledge of applications such as Excel and PowerPoint. Lastly, you master the English language – both in speech and writing.

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 Julie Birk Lauridsen on +45 3079 8729.

Deadline
30 May 2013.

Corporate Procurement 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 new ways of thinking to our company.

Two full time internships in Corporate Procurement are open for placement in a period of 6 months.

About the department
Corporate Procurement is, in close cooperation with affiliates and stakeholders, responsible for the purchasing, sourcing and contracting of the global indirect spend in Novo Nordisk. Corporate Procurement has more than 100 employees organised in 7 departments and is a part of Corporate Finance.

The job
The ideal candidate is studying within the fields of Economics, Sales & Marketing, Project Management, and Engineering or similar at Master level.

You will be involved in sourcing related activities ranging from supplier analysis, establishing data transparency, preparing for negotiations and closing contracts. Further, you can be involved in one or more projects optimising the global sourcing processes. Ad hoc tasks will also be part of the job.

We will strive to define your tasks so you experience sole responsibility for selected areas. But you will of course work in close collaboration with your colleagues and stakeholders.

Qualifications
You have an analytical mind-set and a structured problem-solving approach. You have good verbal and written communication skills in English, and possess a solid level of IT proficiency in MS Office.

You are able to work with many different kinds of people in the organisation, and have an interest in establishing and maintaining relationships with stakeholders - both in Denmark and abroad.

It is a prerequisite that you are an optimistic individual, with a can do attitude. We work as a team with a high energy level and humour. Further you understand the ethical rules and guidelines, under which pharma industry operate.

Finally, you are studying and you are able to use this internship as part of your education.

Contact
For further information, please call Lars Bargsteen Møller on +45 3079 7712 or Peter Dam Madsen on +45 3079 3226.

Deadline
10 June 2013.

Health Economist

• Research & Development
• Denmark - Søborg

Health economics is an important part of obtaining market access for our products. A key challenge for the pharmaceutical industry is to get the healthcare decision makers to support funding of innovative medicines. Such a new environment requires a strong health economic evidence package for our customers.

About the department
Our goal is to generate and document scientific information related to health economics and outcomes research (HEOR) that further increases the value of Novo Nordisk products in addition to quality, safety and efficacy.

HE&HTA aims to bridge commercial aspiration with sound scientific evidence, by providing output that will enable Novo Nordisk to achieve patient access to our products at an optimal price. This involves economic modelling, database studies, patient-reported outcomes (PRO), and HEOR input to clinical trial design.

The job
We are offering a global role that involves a wide range of interesting and challenging assignments, which are related to demonstrating value of our pipeline portfolio. You will be accountable for managing and implementing the HEOR perspective into the Novo Nordisk early drug pipeline. It involves the process of identifying the potential economic profile of drugs at an early development stage in order to support research prioritization and development decisions. You will also manage the integration of HEOR and PRO parameters into the clinical development program, as well as providing an early strategic HEOR/PRO plan. The position requires being up to date on health technology assessment (HTA) trends and requirements.

The candidate we are looking for will be working to support Novo Nordisk’s future inflammation products, for rheumatoid arthritis, Chrohn’s disease etc., that are currently in clinical development.

You will liaise across functions on pricing/reimbursement, HTA and clinical requirements. Therefore superior stakeholder management skills and the ability to communicate technical results in a non-technical way are essential to be successful in this position.

Qualifications
The position requires a Master or Ph.D. degree in Health Economics, Economics, Public Health or another related area.

It is vital that you have a strong scientific background and the ideal candidate will have gained several years of experience in HEOR/PRO qualifying for Principal Scientist role, but we encourage you to apply should your experience be more limited. Relevant experience includes pharmaceutical industry, consultancy and relevant government bodies.

You need to be collaborative and have excellent interpersonal skills. The ability to manage a diverse set of stakeholders and handle projects in a team-oriented/cross-functional environment is necessary. It is important that you are business-oriented, enjoy responsibility and are able to manage working independently, under pressure and within timelines. Furthermore, you need to be a good communicator. Fluency in English is a requirement, as you will work in a global environment with contacts all over the world. International travel will be necessary on occasion as well.

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 Mark Aagren at +45 3079 9976 or Anne Kirstine Busk at +45 3079 9449.

Deadline
2 June 2013.

Senior International Trial Managers

• Research & Development, Trial Manager
• Denmark - Søborg

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, GLP-1 and Obesity is looking for Senior International Trial Managers to join us as we are expanding our activities. We are a team of more than 70 highly skilled and ambitious colleagues responsible for planning and execution of clinical trial activities in accordance with the Clinical Development Plans within diabetes and obesity. 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 chairperson of the Study Group/International Study Group you will organise and execute team meetings and ensure the involvement of relevant stakeholders for decision making. Moreover, you will be instrumental in setting up and running Investigator and Monitor meetings. You have a structured and analytical approach during development of critical trial documents like the trial protocol, 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.

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 as well as good presentation, communication and negotiation skills. A quality mind set is a must, together with a 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 Randi Rahbæk on +45 3079 8419 or Lone Petersen on +45 3075 0947.

Deadline
30 May 2013.

Internal Control Advisor

• Finance
• Denmark - Bagsværd

Do you want to work with a high degree of flexibility, responsibility, influence and interaction within the global Novo Nordisk organisation? If so, now you have the opportunity to join Sarbox Consulting in Corporate Finance HQ. We work within many areas of the finance and IT organisation, which we guide in managing financial reporting risks, structuring and optimising processes, and designing internal controls.

About the department
Our team consists of six ambitious and experienced former auditors in Denmark and four abroad. The team primarily works within Novo Nordisk’s largest business areas, which are the USA, Japan, China, Europe and HQ. The team’s primary responsibility is to ensure that Novo Nordisk has established adequate robust financial processes and controls in compliance with the Sarbanes-Oxley regulations related to financial reporting.

In addition, our knowledge and experience in “best practices” is used to advise and benefit the finance organisations in our medium-sized affiliates in many different aspects. Likewise, we use our knowledge regarding internal controls in other non-financial related areas such as our Social and Environmental reporting and Business Ethics. In close collaboration with line of business, we assist and support their communication with the internal and external auditors. Our work is carried out in close cooperation with colleagues throughout the Novo Nordisk group who are operationally responsible for the business processes and controls. In this way, we develop a wide ranging network across the globe.

The job
We offer you a job that involves several interesting projects with focus on structuring and optimising processes in the largest business areas in the Novo Nordisk group. You will support compliance projects within finance and IT where you are expected to be the expert and the value-adding partner to the business. You will also obtain an exceptional insight into the business areas and principles of the Novo Nordisk group.

You will thrive in a cheerful international working environment with flexible and balanced working hours throughout the year, including around five to six weeks of travel. We offer unique career opportunities in a highly dynamic global environment where you will be given an individual development plan to ensure that you develop both personally and professionally.

Qualifications
You hold a B.Sc. or M.Sc. in auditing, accounting or similar, and have two to four years’ experience working with auditing or assessment of financial processes in a large accounting or international firm. IT knowledge is an advantage and IT flair is a prerequisite. You are an internationally oriented person who can independently perform risk evaluation, analysis and take decisions. You value teamwork as well as communicating with management and stakeholders, and you have the ability to stay focused when working under pressure. You are fluent in both written and spoken English on a professional level, and are willing to travel when the job requires.

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 Danny Kring Krabbe at +45 3079 4787.

Deadline
31 May 2013

Internship opportunity in Global Medical Affairs Study Programmes, Nov

• 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
Study Programmes is an international team of project managers with diverse personalities and backgrounds (project management, marketing, communication and clinical development). We provide innovative communication support to complex clinical trials, which are critical for the success of Novo Nordisk’s current and future product portfolio. To achieve trial success, we drive external partnerships with scientific experts, trial investigators and study coordinators, and tailor patient recruitment and retention initiatives based on their inputs. As facilitators of internal collaboration, we coordinate and liaise across project functions globally and locally, reinforcing stakeholder engagement and thereby the alignment of initiatives driven.

The job
Your main responsibility will be to support and drive the implementation of planned recruitment and retention activities. Key tasks for you to execute will include the following:

Coordinate logistics to support implementation of planned global meetings, typically involving medical and scientific experts otherwise known as Key Opinion Leaders (KOLs) from the Diabetes industry.

Develop toolboxes to support the roll-out of patient recruitment and retention tools for affiliates to adapt and implement locally.

Leverage established internal channels to manage communications with colleagues located across the globe.

Manage collaboration with vendors, with an opportunity to innovate processes and negotiate terms when relevant.

At the global and local level you will liaise with multiple cross-functional stakeholders, granting you insights to how Novo Nordisk’s project-based organisations function. Considering the global scope of your responsibilities, a few travelling days can be expected during your internship period. This brings you to the forefronts of our activities, where the exposure and inherent key learnings will be priceless.

Qualifications
You are pursuing a relevant business or science degree, either on your first or second year. Knowledge of and some experience in project management is vital, and an interest in treating diabetes is preferable.

You are able to work on multiple tasks in parallel and cope well under time pressure while maintaining your sense of humour.

You are comfortable working in a dynamic environment and have excellent interpersonal skills. A reference of successful collaboration and influence on multicultural and multidisciplinary stakeholders would be favoured.

You have good communication and presentation skills as well as a strong command of English, both written and spoken. You are a strong team player with sense of urgency.

Practicalities

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: 02 September 2013

Contact
For further information, please call Jan Kildeskov on +45 3079 0069.

Deadline
10 June 2013.

Internship in Sales and Marketing Excellence, Novo Nordisk

• 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
In Sales and Marketing Excellence we work to advance the way we most effectively bring the value of our innovative medicines to patients. We operate in a global cross-functional environment - across countries, product teams and functions - to ensure stronger processes and capabilities. We service the global marketing organisation with concepts such as the Novo Nordisk Marketing Academy for Excellence (G-MAX) and manage key governance functions such as the Global Sales Forum, PMComm (Lifecycle Management Committee) and the Biosimilar Commercial Group. Finally, we drive a wide array of commercial excellence projects, including development of innovative ways to strengthen the link between Marketing and Sales.

The job
By joining the Sales and Marketing Excellence team you will get a unique opportunity to dive into novel ways of doing global marketing and sales. By supporting the establishment and implementation of key projects and offers you will learn about overall commercial processes and methods. You will be an integral part of our core team and tasks will vary from strategic and longer term to ad hoc practical support.

Qualifications
We are looking for an intern who is passionate about marketing and sales. You can drive projects independently taking a methodical

approach to your work and tasks, but demonstrating flexibility when priorities change. In addition, you enjoy being busy and maintain

a can-do positive spirit through times of pressure.

You are currently in your first or second year of studying on your master degree in business, or a related field. You already have some experience with cross-functional project management either in a work or academic setting. You have excellent interpersonal and communication skills. You must be fluent in both oral and written English.

Practicalities

Bachelor degree in business or a related field.

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

Start date: August/September 2013.

Contact
For further information, please call Asger Jacobsen on +45 3079 0161.

Deadline
10 June 2013.

Internship in Customer Insights, Global Marketing

• 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 have the opportunity to join an international, high performing team responsible for generating customer insight (being physicians and patients) and utilise the insight 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 Project Managers in the Customer Insight team in anonymised, patient level data analysis. In this role, you will be programming in SAS base, working with data mining, generating market insight and communicating the insight to relevant internal stakeholders. You will also work alongside Global Project Managers and Global Product Managers, in analysing market dynamics and providing input of customer insight 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. Usage of SAS, fluency in both oral and written English and excellent interpersonal skills are required. General knowledge about pharmaceutical industry 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.

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: 01.08.2013

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

Deadline
10 June 2013

Internship in Drug Product Development Business Support, Novo Nordisk

• 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
Novo Nordisk is seeking an engaged student for a full time internship to Drug Product (DP) Development Business Support in a period of 4-6 months. DP Development is part of Chemistry Manufacturing and Control (CMC) Supply, which manufacture and distribute drug candidates for pre- and clinical trials, develop commercial manufacturing processes and technologies and produce approvable scientific documentation. DP Development is an organisation with close to 370 employees all located in Denmark.

The job
You will be working in a young and dynamic business support team with 7 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 in DP Development Business Support 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 4-6 months.

Start date: 1 August 2013

Contact
For further information, please contact Linnéa Kroon +45 3079 3215.

Deadline
10 June 2013

Internship in Corporate Sustainability

• 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 master students who bring new ways of thinking to our company.

About the department
For more than 20 years, Novo Nordisk has had a strategic commitment to be a sustainable business and this has brought the company onto centre stage as a global leader, evidenced by numerous recognitions and top rankings in benchmarks for good sustainability performance.

As an intern in Corporate Sustainability, you have the opportunity to join one of the most innovative sustainability departments in the world and work with a dedicated team of 16 employees. You will get first-hand knowledge on how to integrate sustainability in a multinational company and you will have an opportunity to support the team working with the integrated annual report - a reporting method that Novo Nordisk continues to receive international recognition for.

The job
You will provide daily assistance to the team in charge of the Novo Nordisk’ integrated annual report. (The task will not include writing.) You will be working on integrating sustainability in line of business, which includes qualitative and quantitative data gathering and writing of summary reports. You will also be involved in ad hoc communication and research tasks.

Qualifications
You are a master degree student in Business Administration, Communication, Strategy, Corporate Sustainability or similar in the first or second year of your master studies, and take an interest in Corporate Sustainability and project management. (Please note that full-trained candidates cannot apply for the position). You are among the best in your class, proficient in English and are used to both working independently and in teams. You have previous experience from working in a private company and are a solid communicator in both word and powerpoint and familiar with Excel.

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

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

Period: The internship is full time (37 hours per week), preferably for 6 months.

Start date: 1 August 2013.

Contact
For further information, please call Annemarie Meisling on +45 3079 6243.

Deadline
10 June 2013.

Internship in DMS Finance

• 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.

Practicalities

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 2013

Contact
For further information, please call Anders Hvidt on +45 3075 4023.

Deadline
10 June 2013.

cLEAN Partner

• LEAN
• Denmark - Bagsværd

Do you have experience in breaking down tough business challenges then applying LEAN tools and concepts to solve them? Can you coach leaders to change their behaviour and challenge how they do business? And are you equally comfortable managing a project or coaching a project manager to get results? Then we need you to join our group of cLEAN® Partners in Site Denmark (SDK), filling one of 3 remaining openings in our team.

About the department
We are recruiting for cLEAN® Partners in 3 different departments in Site Denmark: Quality, Quality Control, and Environmental Monitoring. Quality Assurance, with ~220 employees covering three production sites, is responsible for of the ensuring our processes and product are at the highest level of compliance to regulatory requirements. Quality Control, with ~95 employees in two locations, has the vital task to test the quality of our product to ensure our processes are in control at all times. Environmental Monitoring, with ~50 employees in two locations, has the responsibility to ensure our aseptic production areas provide the sterile environment needed to make a life-saving drug for injection.

The job
As cLEAN® Partner your main role will be to continuously develop LEAN mind-set and drive improvement of LEAN behaviour to solve business challenges across SDK. You will spend most of your time on the shop floor, supporting leaders in developing their systems and behaviour to drive continuous improvement. To do this, you will work both as part of a site wide team of cLEAN® Partners and together with the HR and Training Partners within your assigned area.

You will be responsible for developing the systems (e.g. performance boards, problem solving, process confirmation) used by leaders in your area to see, solve, and follow-up on problems, in a way that secures sustainable results and coaching the behaviour needed to use and continuously improve these systems.

Qualifications
You hold a BSc. or similar undergraduate degree, but a MSc. or MA within engineering, business, or economics is preferred. It is absolutely essential that you have strong analytical skills and as well as the ability coach and challenge leaders, in order to have them set a clear direction for their area. You are able to drive processes proactively in a complex production environment with many stakeholders and you enjoy building relations across organisational areas and levels. Experience with applying LEAN manufacturing concepts, and the change management to sustain implementation, as well as project management is a prerequisite. Based on your experience in handling high complexity you are able to prioritise and deliver results without compromising the overall focus and priorities across the organisation. On a personal level, you are a self-starter, and you thrive driving your tasks independently. To succeed in this position you must possess a strong personal drive.

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 Ken Gray at +45 3075 6155 or Carsten Frank at +45 3075 1485.

Deadline
1 June 2013.

Internship in Global Marketing Devices, Novo Nordisk

• 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
Our team works with the global marketing activities of our portfolio of current and future devices and needles. We work on developing strategies and tactics in close collaboration with our colleagues in the other global marketing brand teams. We support the implementation of tactics in our regions and locally. Our team interacts with internal and external stakeholders. Internally, we are supporting the drug brand teams for both marketed and future medications. We have a lot of interaction with our colleagues in the countries around the world. We are a main input giver to device life cycle management activities as well as future device innovation projects. Finally, we’re collaborating with a variety of other functions including medical affairs, product supply, regulatory affairs etc. Our external interaction is mainly with marketing research, advertising agencies etc. We’re an international team of highly skilled, high performing project managers working toward making our devices the most preferred in the market.

The job
Professionally you will participate and get experience from working with the development and roll-out of promotional and other materials for our marketed devices. You will be involved and supporting our team members in their day to day liaison with affiliates with regards to marketed devices. Specific projects/tasks to be decided e.g. support to NovoPen® 5 launch planning and execution, launch coordination of FlexTouch®, launch support to specific markets, participation in development of Life Cycle Management activities for our devices etc.

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
We are looking for an intern who is passionate about pharmaceutical marketing and communication. You are currently studying on your master’s degree in marketing, business, economy, pharmacy, engineering or another relevant field. General knowledge of marketing related disciplines and key methodologies (marketing, communication, strategic and tactical planning, market research methodologies) preferred. 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; 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

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 2013

Contact
For further information, please call Anders Krabbe on +45 3075 6179.

Deadline
10 June 2013.

Internship in Site Denmark Logistics

• 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
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 July/August 2013 (preferable 15th of July). 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 nine 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 systematic 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 Master´s or Bachelor’s degree in Production Engineering, Logistics, Supply Chain management or any other relevant degree, and you are among the best in your class. 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.

Contact

Contact
For further information, please contact Carl Johan af Rosenborg on +45 3075 6719.

Deadline
10 June 2013.

Internship in Product Supply University

• 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
At Novo Nordisk's production area Product Supply (PS), PS University is responsible for the development and delivery of training across the global organization. The PS University Trainers Academy offers targeted competency development for trainers throughout the organization in order to support PS in reaching its business goals. The Trainers Academy provides train-the-trainer activities to support internal trainers conducting Classroom Training, Shop Floor Training and Virtual Training – and is now initiating a project to enable the organization to work effectively with eLearning. We are now looking for the right person to take on the role as intern to support this project. If you are dedicated to learning, training and competency development this might be the position for you.

The Job
Your job will be to support our HR development consultants in building a Train-the-trainer program for eLearning authors, and to develop a web-based toolbox that supports professionalization of using eLearning in Product Supply. You will support the project team throughout the project, and be able to work with your own projects depending on your competencies and areas of interest. There will be plenty of opportunities to get a good insight in many other aspects of working with competence development in a global organization.

Qualifications
We expect you to have a passion for Human Resource Development and wish to pursue a career within HR when you finish your studies. Further, you have a good understanding of business processes and know how the HR function relates to the business. You are probably studying HA/Cand.Merc.(psyk.), HA/Cand. Merc.(Com), Cand.Merc.HRM or similar. This however, is not a requirement to apply for the position. We also expect that you have a good understanding and preferably hands-on experience with eLearning and/or web-development.In order to be successful in the position you should possess the following characteristics: You are ambitious and engaged. You take a systematic approach to the tasks and consider the job as more than just a job, and are able to work independently without neglecting the importance of being a team player.You thrive in a global environment, and you have good communication skills and speak and write both English and Danish fluently. You have IT flair master the Microsoft Office Package. Talent for graphical design will be an extra plus.

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: September 2, 2013

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 Henriksen on +45 3079 7561.

Deadline
10 June 2013

Management Assistant

• Administrative
• Denmark - Søborg

Clinical Operations, Degludec, is seeking a new colleague to take up a position as Management Assistant in Søborg.

About the department
We have a team of experienced and enthusiastic International Trial Managers and Clinical Trial Administrators who is responsible for planning and conducting clinical trials within the diabetes area, in close collaboration with Novo Nordisk affiliates all over the world.

Our work environment is characterised by exciting new challenges, a global network, knowledge sharing and continuous professional and personal development which comes when working for a large headquarter function.

The job
You will act as Management Assistant to the Head of Clinical Operations, Degludec1 and Head of Clinical Operations, Degludec2. You will be responsible for a broad spectrum of administrative tasks connected to the departments and also for maintaining the department documentation in compliance with Novo Nordisk standards. Other tasks include calendar management, travel arrangements, handling of human resource issues, coordination of monthly report input, arrangement of department meetings and seminars, taking meeting minutes and prepare graphic presentations as needed. The department budgets will be monitored by you.

Qualifications
You can proactively take action and ownership for tasks and decisions and welcome new responsibilities. Your coordination skills and overview is above average, while at the same time having a structured approach. You cooperate with people within and outside your own work area to achieve business goals, sharing learning, knowledge and skills and promoting cross-functional teamwork. You have excellent communication skills and a genuine desire to collaborate across boundaries. You adapt easily to a changing environment and shifting demands, and you are eager to contribute to the continuous development of the department. You are able to handle confidential information and last but not least you have high spirits.

Your educational background includes a bachelor degree, with at least 3 years experience in an administrative position preferably from an international business environment. You are proficient with both written and spoken English. You like to be part of a multi-cultural team, working with multiple and frequently changing priorities. You are highly skilled with MS Office and SAP and find it easy to master new IT systems.

In Novo Nordisk 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 Cecilie Hedvig Valet on +45 3075 2156 or Sune Aggergaard on +45 3075 8446.

Deadline
26 May 2013.

Internship in Business Support, Strategic Sourcing

• 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
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 Hillerød, where 7 competent colleagues look forward to welcoming you.

The job
As intern in Business Support your job will be to manage minor projects and act as support to larger projects in the department. Furthermore, you will be supporting some of our standard reporting processes within finance and risk management. 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.

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 2013

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

Deadline
10 June 2013

Internship in Changing Diabetes®

• 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
Changing Diabetes® is a team within Global Marketing, which sits in Marketing & Medical Affairs at Novo Nordisk A/S. You will join a team responsible for leading the leveraging of the corporate brand, via market shaping, market access & supporting the business objectives for all the Diabetes brands.

The job
As part of the team you will support development, and ensure implementation of global marketing strategy for Changing Diabetes®. You will be expected to support the development of innovative marketing activities and programmes to support the Changing Diabetes® brand, working on exciting projects such as the Changing Diabetes Barometer & the DAWN2 programme. In addition you will work on a fantastic sports sponsorship programme of a team of all diabetes professional cyclists, Team Novo Nordisk, developing programmes and materials to support their mission to educate, empower and inspire about Diabetes. Specifically, you will support the development and implementation of compelling campaign material, education programmes benchmarking analysis and business process improvement to leverage Changing Diabetes and driving differentiation from competitors. You will also have the opportunity to support the collaboration with key affiliates. 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 marketing, project management and effective (internal and external) communication. You are currently in your first or second year of studying on your master degree in communication, business, or related fields. You already have some experience with cross-functional project management either in a work or academic setting. You take a methodical approach to your work and tasks, but demonstrate flexibility when priorities change. 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 have professional and personal impact that is reflected in your desire to take initiative and responsibility for your projects.

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: Aug / Sep 2013

Contact
For further information, please contact Debbie Bevan +45 3079 9865.

Deadline
10 June 2013.

Internship in Global Levemir® Marketing

• 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
Levemir® Global Marketing is a team within Global Marketing, which sits in Operations at Novo Nordisk A/S. You will join a team responsible for leading the global brand strategies for Levemir, growing volume and value market share for Levemir, and driving investments to secure its acceleration to double blockbuster status by 2014.

The job
As part of the team you will support development, and ensure implementation of global marketing strategy for Levemir®. You will be expected to support the development of innovative marketing activities and programmes to support Levemir®, our current modern insulin portfolio and our future portfolio. Specifically, you will support the development and implementation of compelling campaign material, education programmes benchmarking analysis and business process improvement to accelerate growth of Levemir®, driving differentiation from competitors. You will also have the opportunity to support the collaboration with key affiliates. 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 marketing, project management and effective (internal and external) communication. You are currently in your first or second year of studying on your master degree in communication, business, or related fields. You already have some experience with cross-functional project management either in a work or academic setting.

You take a methodical approach to your work and tasks, but demonstrate flexibility when priorities change. 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

have professional and personal impact that is reflected in your desire to take initiative and responsibility for your projects.

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: 12-AUG-2013

Contact
For further information, please contact Adam Burt +45 3079 5111.

Deadline
10 June 2013.

Internship in Corporate Occupational Health and Safety, 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 exiting learning opportunities for students who bring new ways of thinking to our company.

About the department
The job is located in Corporate Occupational Health and Safety (COHS) which is a corporate staff function. COHS is Novo Nordisk’s Centre of Excellence in the field of occupational health and safety globally with 28 dedicated colleagues working in the areas of occupational medicine, employee health programme, psychosocial and physical working environment. COHS’ role is to inspire and support the OH&S work in the global organisation, enabling line of business in making Novo Nordisk’s OH&S ambitions come true and providing easy-to-use knowledge, tools and data.

The job
We offer a challenging internship with focus on global communication of OH&S. In this role your main key task will be to communicate complex matters in a simple way. You will perform stakeholder interviews and analysis to help develop good communication to the organisation globally.

Qualifications
We are looking for an intern who is passionate about communication. You are currently studying on your master’s degree in communication or the like. You have knowledge of communication via intranet to colleagues globally and different cultures. Ability to design excellent presentations is important.

We expect candidates to thrive in a busy environment, bring a can-do attitude and a healthy sense of humour to your work even when the pressure is on. Fluency in both oral and written English; ability to manage global projects (with supervision) sound personal judgment; and 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 a strong work ethic and willingness to take responsibility for your own learning.

We will provide you with relevant knowledge of OH&S work for your internship.

Practicalities

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: August/September 2013.

Contact
For further information, please call Judith Hellsten on +45 3079 1403.

Deadline
10 June 2013.

Internship in Communication

• 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
Diabetes API is part of Novo Nordisk Product Supply and is responsible for the production of the active pharmaceutical ingredients in the insulin manufactured by Novo Nordisk. The area compromises nine factories, among these the largest insulin production facility in the world. With reference to our communication partner you will be part of a cross functional HR/communication team, which has the responsibility of developing and implementing the people and communication strategies for Diabetes API.

The job
In Diabetes API you will be working with a wide range of internal communication tasks incl. developing our intranet and other internal communication platforms. Furthermore, you will engage in organising events, providing communication advice and support to stakeholders in the organisation, writing news stories for our intranet and magazine, and other day to day tasks.

Qualifications
You are in your first or second year of your Master programme within Communications. You are a skilled communicator who is comfortable speaking and writing in English. In addition, you have solid IT skills and you are eager to explore new ways of engaging employees in internal business communication and knowledge sharing. You are organised, a good planner and a proactive problem-solver. You are responsible and have and a huge drive and you understand how to act in a large organisation with many stakeholders. You are driven by the creation of results in close relations with others and think in possibilities, instead of challenges. You have daily contact with many different stakeholders, and solid communication, interpersonal and network skills are therefore a necessity in order to be successful in the job. Last, but not least you speak and write English on a high level.

Practicalities

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

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

Contact
For further information, please contact Stine Gry Roland at +45 3075 0567.

Deadline
10 June 2013.

Internship in PS Operator Recruitment Centre

• 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 be part of HR Operations responsible for supporting all Novo Nordisk’s production sites in Denmark. In Operators Recruitment Centre (ORC) we are a team of highly skilled Recruitment Partners who support hiring managers during the recruitment process. Furthermore, we continuously build pipeline of operator vacancies to meet future recruitment needs. As our processes are fast and efficient, you will be able to read the results of your work almost immediately.

The job
Your primary task will be to drive a project reviewing the department’s services from the line of business’ point of view. To this end, you will plan and conduct interviews with the hiring managers to produce data for your analyses, as well as you analyse candidates’ questionnaire responses. Concurrently, you can foresee different tasks related to handling of candidates, including screening, calling in for interviews, participating in meetings, etc. You will support your colleagues in their analytical work to help ensure that no stone is left unturned. As part of this, you will help put together an applicable structure for the handling of data in the department in general. Naturally, you will work in close sparring with your team colleagues and have contact to various job-seeking operators. This is an opportunity to gain vast insight into a recruitment environment where we reward the responsibility you take with the latitude to plan and organise your workday.

Qualifications
You are studying for a Master’s degree within the Social Sciences, Psychology, HR, Communication or similar. Moreover, you are well-versed in MS Office and have convincingly strong communication skills in Danish and English. It will be a plus if you have experience uncovering user needs or have worked with surveys in your studies or a student job. You have an open attitude and recognise yourself as a proactive person with a strong will to follow through. A sound overview and capability to juggle several tasks simultaneously are necessary, and to this end, you will need the ability to structure your work. To top it off, we would also like to hear from you if you have experience developing efficient tools for business processes and processes in general.

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 or 1 September 2013

Contact
For further information, please contact Mette Søllested at +45 3075 2430.

Deadline
10 June 2013.

Internship in Regulatory Academy

• 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
Regulatory Affairs is responsible for global strategies to obtain and maintain market authorisations worldwide for all Novo Nordisk's new products and for life cycle management activities such as new medical indications, new or changed production methods, or new facilities. Regulatory Affairs also carries responsibility for labelling of Novo Nordisk products. You get the opportunity to join an international, high performing Regulatory Academy team in Søborg, Denmark, responsible for providing contemporary regulatory training and competence development opportunities internally in Novo Nordisk.

The job
Regulatory Academy develops and offer training in close collaboration with key internal stakeholders in Regulatory Affairs. You will assist the training specialists in day-to-day business processes and tasks. You will be involved in updating the strategy for the internal training in Regulatory Affairs, and assist with analysing our current training management set-up.

Qualifications
We are looking for an intern who is passionate about training and competency development. You are currently studying on your master’s degree in training, communication or other relevant field. 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; ability to manage a large volume of projects (with supervision); sound personal judgment; and excellent interpersonal skills are required.

Finally, you must have strong work ethic and willingness to take responsibility for your own learning.

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.

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: 1 September 2013

Contact
For further information, please contact Lena Munk on +45 3079 6098.

Deadline
10 June 2013.

Communication Internship in Regulatory Affairs, Novo Nordisk

• 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
Strategic Management Support is a staff function within Regulatory Affairs in Novo Nordisk Research & Development. Working in Regulatory Affairs Strategic Management Support means navigating in a fast-paced global environment where no two days are alike. Tight deadlines, cross-organisational collaboration, project management and the challenges of communicating with stakeholders in 70+ countries is part of our busy workday.

The job
In Regulatory Affairs Strategic Management Support you will be working with a wide range of internal communication tasks incl. developing our intranet and other internal communication platforms. Furthermore, you will engage in organising events, providing communication advice and support to our organisation, writing news stories for our intranet, analysing our stakeholder relations and other day to day staff function tasks.

Qualifications
You are in your first or second year of your Master programme within Communications or IT. You have solid IT skills and you are eager to explore new ways of engaging employees in internal business communication and knowledge sharing, e.g. through social media. You are organised, a good planner and a proactive problem-solver, and you’re a skilled communicator who is comfortable speaking and writing in English. As a person, you thrive in busy environments and bring a can-do spirit and a healthy sense of humour to your work – even when the pressure is on. You’re a strong team player, but you also enjoy working independently and finding new solutions to the challenges you meet. You are expected to make an impact and to ask questions and challenge the status quo if that’s what it takes.

Practicalities

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

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

Start date: 1 September 2013.

Contact
For further information, please contact Jakob Wolter +45 3079 7759 or Jakob I. Jensen on +45 3079 3815.

Deadline
10 June 2013.

LEAN and Quality Internship in Regulatory Affairs

• 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
Regulatory Affairs Strategic Management Support is a staff function within Novo Nordisk Research & Development. Working in Regulatory Affairs Strategic Management Support means navigating in a fast-paced global environment where no two days are alike. Tight deadlines, cross-organisational collaboration, project management and the challenges of communicating with stakeholders in 70+ countries is part of our busy workday.

The job
In Regulatory Affairs Strategic Management Support you will be working with improvement projects (LEAN) and Quality Management tasks. Focus will be on standardising internal processes and establishing transparency across functions. Examples of tasks could be the mapping of internal processes, providing Regulatory Affairs management with data on progress of projects and activities, improving communication with internal stakeholders regarding LEAN and Quality Management, ad hoc analytical and administrative tasks.

Qualifications
You are in your first or second year of your Master programme within business, technical, or natural science studies. You are driven by a wish to do things smarter and to optimise work processes. You are detail oriented, a good planner and a proactive data driven problem-solver. You are a skilled communicator who is comfortable speaking and writing in English. As a person, you thrive in busy environments and bring a can-do spirit and a healthy sense of humour to your work – even when the pressure is on. You are a strong team player, but you also enjoy working independently and finding new solutions to the challenges you meet. You are expected to make an impact and to ask questions and challenge the status quo if that’s what it takes.

Practicalities

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

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

Start date: 1 September 2013.

Contact
For further information, please contact Marina Stokholm Bryld +45 3075 7338 or Lene Thrane on +45 3079 9510.

Deadline
10 June 2013.

Internship in Finance Projects

• Finance
• Denmark - Bagsværd

Novo Nordisk is one of the world’s most successful pharmaceutical companies. The vision of global finance is to be the best finance operation in the global pharma industry. Finance Projects is an internal consultancy, which supports the vision by driving a number of key projects throughout Novo Nordisk’s global organisation.

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 master 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 or with previous Novo Nordisk experience.

In your work you will be widely exposed to the Global Finance organisation in Novo Nordisk, and get hands-on experience with best practice project management methods and tools.

The job
As an intern in Finance Projects, 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 a master degree student in Economics, Business Administration, Engineering or similar in the first or second year of your studies, and take an interest in consulting, corporate finance and project management. You are among the best in your class, proficient in English and are used to both working independently and in teams. Finally you have a positive attitude.

Your development is important to us. Training and personal development plans are key tools to ensure your tasks continue to challenge you while developing or sharpening your toolbox. The position implies a possibility of permanent employment with Novo Nordisk after completion of education.

Practicalities:

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

Start date: 1 August 2013.

Contact
For further information, please contact Rasmus Maltha on + 45 3079 3323.

Deadline
10 June 2013.

Internship in Device Research and Development

• 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 and Development (DRD) is a R&D area responsible for developing novel injection systems that enable people with diabetes to make self-treatment.

You get the opportunity to join an ambitious development team in Hillerød working on a future injection device platform. As a team we strive to be a highly professional and innovative unit that is able to maintain a playful environment while still having a clear focus on progress and results.

The job
You will have the opportunity to be part of the innovation process ranging from the initial creative phases all the way to outlining the final development candidate. As R&D engineer you will be part of outlining device concepts and mechanical details that fulfils the user needs. In this role you will perform conceptual ideation, mechanism design and calculations as well as CAD (Computer Aided Design).

Qualifications
We are looking for an intern who is passionate about mechanical engineering and innovation. You are currently studying on your master’s degree in mechanical engineering, design & innovation or other relevant field. General knowledge of conceptualization, mechanical engineering, CAD preferred. 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; ability to manage a numerous numbers of project tasks (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: 12. August 2013

Contact
For further information, please contact Søren Steenfeldt-Jensen +45 3075 8970.

Deadline
10 June 2013

Internship in Global Talent Attraction

• 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 12 employees with a variety of backgrounds (HR, communication, marketing and international business). We use our differences to create novel ideas and high-quality solutions.

The job
We have a constant focus on optimizing 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 have some experience with branding or event management. Some knowledge with Photoshop and/or InDesign would 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.

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 September 2013

Contact
For further information, please contact Sarah Marie Andreasen Bovbjerg +45 3079 2163.

Deadline
10 June 2013.

Team Leader

• Research & Development
• Denmark - Gentofte

A challenging and varied position in CMC DP Development is available for a dynamic and skilful Team Leader. You will join a R&D department responsible for project management and formulation development of new biopharmaceutical drugs. The project pipeline is expanding and this offers a unique opportunity to participate in an innovative and exciting period where new projects and challenges are part of the everyday work.

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 department consists of 2 teams; the open position is in team Biopharm Formulation Development I, which is involved in project management and drug product formulation development within the haemostasis projects. The team consists of 22 highly skilled and experienced project managers, specialists, formulation scientists and technicians. The department is located in Gentofte.

The Job
You will be responsible for the performance of the team to meet and exceed project and organisational goals. You will ensure effective resource allocation in your team, and you will be the one to encourage and facilitate professional discussions. You will provide leadership and spur continuous development of the team members through coaching and dialogue. You will be a member of the management team of Biopharm Formulation Development, which consists of a department manager and two Team Leaders - and you will participate in cross organizational projects and collaborations. You will lead the way and be a role model in a LEAN culture, openness, honesty and focus on continuous improvements being a natural part of your personality. The work in Biopharm Formulation Development has a strong focus on scientific skills and the environment is dynamic, engaged and with a social atmosphere.

Qualifications
You hold a PhD or equivalent in Biochemistry, Chemical Engineering, Pharmacy or other relevant scientific discipline. You have proven practical experience in protein chemisty and formulation development. You have proven strong leadership skills and you are expected to have a minimum of 2 years people management experience from the pharmaceutical industry. On the personal level you have an open, innovative mindset and ability to work effectively in a team-oriented setting. You have a can-do mind-set and focus on opportunities rather than on limitations and you provide the right balance between leadership and management to your team. You have excellent oral and written communication skills. We offer you exciting work challenges and the opportunity for professional and personal development in an ambitious functional area – and the opportunity to be a part of Novo Nordisk international R&D organization.

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 Malin Gustavsson at +45 3079 4524.

Deadline
31 May 2013.

Product Surveillance Advisor

• Quality
• Denmark - Bagsværd

In this job, people worldwide depend on you to keep an eye out for their safety and to take action if it is needed. If you find this challenging and inspiring, then you might be our new colleague in Global Safety.

About the department
Customer Complaint Center (CCC) is looking for a product surveillance advisor to perform surveillance of complaints globally and to handle product recall situations. The job is a permanent position starting 1st of August 2013. Our department is as a part of Global Safety responsible for the surveillance of Novo Nordisk products globally.

We are located in House of Quality in Bagsværd.

The job
You will be responsible for surveillance and trending of customer complaints and for managing product recall situations.

An important part of the surveillance responsibility is reporting and presenting trends to top management and various management forums, e.g. preparation of quarterly reports and presentation at Quality Management Review. We are also represented in various committees, e.g. Safety committees and Complaint Surveillance Groups. In product recall situations you will be responsible of coordinating all relevant investigations and activities and to handle contact with regulatory authorities such as the FDA and EMA. Therefore, a job in CCC provides an opportunity for working broadly within Novo Nordisk and you will be our link to R&D, production sites, marketing departments and several of our international affiliates. Furthermore, CCC has a high focus on continuous improvement and you will be involved in various optimization projects in the department.

Qualifications
You hold an academic degree in pharmaceutical sciences, engineering or a related discipline and you have a strong quality mindset.

Your analytical skills are excellent, and you can navigate in an organization under difficult circumstances and ensure a high level of communication. In your previous assignments you have demonstrated solid skills in writing reports and making presentations. You are a positive and open minded team player who can co-operate at all organizational levels. You like a dynamic environment with many simultaneous tasks and changing priorities, while managing strict deadlines and meeting business targets. Profound communication skills are required and you are fluent in English, both written and spoken. We offer a very exciting job amongst 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, please contact Lisbet Bærentzen at +45 3079 8080.

Deadline
26 May 2013

Internship in Global Medical Affairs Strategic Operations

• 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
You will support a medical team in Global Medical Affairs with the optimisation of business processes and other day-to-day tasks. You will be responsible for setting up a control room for some of our key brands to ensure effective tracking of medical activities and key performance indicators, as well as preparing management status reports. Day-to-days tasks include among others project management of vendors and updating of training material (content and platform). 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.

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: 02 September 2013

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

Deadline
10 June 2013.

Proces supporter

• Produktion
• Danmark - Kalundborg

Kunne du tænke dig, sammen med engagerede og fagligt ambitiøse kolleger, at være med til at bygge en helt ny afdeling i Kalundborg op? Det nye pakkeri er en strategisk vigtig satsning i Biopharm, der skal sikre den fremtidige kapacitet til at pakke alle 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 og håndtere projektfasen for en ny pakkelinie, der skal levere til markedet allerede i Q4 2013.Er produktionssupport, problemløsning og procesoptimeringer det, der gør hverdag spændende og udfordrende? Og lægger du samtidig vægt på, at det sker det på en struktureret og LEAN måde, så de gode idéer forankres i hverdagen?

Om afdelingen
Biopharm T&FP, Kalundborg er en del af Biopharmaceuticals (Biopharm). Afdelingen består pt. af ca. 20 dygtige medarbejdere, der alle beskæftiger sig med pakning af NovoSeven® og på sigt flere hæmofiliprodukter og GlucaGen® Hypokit. Afdelingen forventes at vokse betragteligt over de kommende år.Dine kommende kolleger består af ingeniører, farmakonomer, automatik- og tekniske supportere, projektledere, operatører, og håndværkere. Afdelingen er opdelt i 2 teams, et produktionsteam og et supportteam. Dit kommende team, Team Support, er en supportfunktion for produktionen, der varetager både GMP-mæssige og tekniske opgaver.

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. Dit arbejde vil bl.a. bestå i support til produktionen, udarbejdelse af afvigelser, ændringssager, trendrapporter, SOP opdateringer, interne reklamationer, samt selvstændigt at drive LEAN-aktiviteter, som f.eks. systematisk problemløsning og proceskonfirmering. Du vil også være en af de supportere der beskæftiger sig med frigivelsen af vores produkter.Din arbejdsdag vil således være afvekslende og til tider hektisk, da driften af vores fuldautomatiserede pakkelinie 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
Du har en relevant videnskabelig baggrund som farmaceut, produktions-, kemi- eller maskiningeniør. Gerne med 3-4 års erfaring indenfor færdigvareproduktion af medico- eller medicinalprodukter, men nyuddannede kan også komme i betragtning til stillingen. Du må gerne have stor og dokumenteret forståelse for GMP. Det vil være en fordel, hvis du har erfaring med brug af LEAN i forbindelse med systematisk problemløsning.Du tager ansvar og finder løsninger i selv pressede situationer og sikrer samtidig involvering og ejerskab blandt dine kollegaer. Som person er du kendt for at være positiv og løsningsorienteret, og god til at etablere samarbejde på tværs af faggrænser. Du er åben og ærlig, samt 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. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel 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 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 Morten Kring på +45 3075 2694.

Ansøgningsfrist
15. juli 2013

Proces Ingeniør

• Produktion
• Danmark - Kalundborg

Procesingeniør til Novo Nordisks nye pakkeri. Kunne du tænke dig, sammen med engagerede og fagligt ambitiøse kolleger, at være med til at bygge en helt ny afdeling i Kalundborg op? Det nye pakkeri er en strategisk vigtig satsning i Biopharm, der skal sikre den fremtidige kapacitet til at pakke alle 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 og håndtere projektfasen for en ny pakkelinie, der skal levere til markedet allerede i Q4 2013. Er optimeringer, problemløsning og teknisk support det, der gør din hverdag spændende og udfordrende? Og ser du implementering af løbende forbedringer, baseret på en struktureret LEAN tankegang, som en naturlig del af det du gerne vil beskæftige dig med?

Om afdelingen
Biopharm T&FP, Kalundborg er en del af Biopharmaceuticals (Biopharm). Afdelingen består pt. af ca. 20 dygtige medarbejdere, der alle beskæftiger sig med pakning af NovoSeven® og på sigt flere hæmofiliprodukter og GlucaGen® Hypokit. Afdelingen forventes at vokse betragteligt over de kommende år. Dine kommende kolleger består af ingeniører, farmakonomer, automatik- og tekniske supportere, projektledere, operatører, og håndværkere. Afdelingen er opdelt i 2 teams, et produktionsteam og et supportteam. Dit kommende team, Team Support, er en supportfunktion for produktionen, der varetager både GMP-mæssige og tekniske opgaver.

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. Dit bidrag vil bl.a. bestå i fejlsøgning på udstyr og gennemførelse af mindre projekter i forbindelse med ændringer/optimeringer af eksisterende udstyr samt i forbindelse med indførslen af nyt udstyr. Derudover skal du foretage udstyrskvalificeringer, opdatering af anlægsdokumentation, udarbejde afvigelser, SOP’er, protokoller og rapporter. På sigt vil jobbet medføre at du vil blive udstyrsansvarlig på vores DV0297 linie, der pakker NovoSeven®. Din arbejdsdag vil være afvekslende og til tider hektisk, da driften af vores fuldautomatiserede pakkelinie 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
Vi er på udkig efter en engageret, motiveret, selvstændig og kvalitetsbevidst produktions- eller maskiningeniør, eventuelt en person med en anden faglig baggrund, der har dokumenteret erfaring indenfor pakketeknologi. Vi ser gerne, at du har 3-4 års erfaring indenfor færdigvareproduktion af medico- eller medicinalprodukter, men nyuddannede kan også komme i betragtning. Det er en fordel hvis du har forståelse for GMP. Det vil være en klar fordel, hvis du har erfaring med pakketeknologi, projektledelse af mindre tekniske projekter og/eller kvalificering og validering af pakke- eller vision-udstyr. Vi ser også gerne, at du har erfaring med brug af LEAN-værktøjer, som f.eks. systematisk problemløsning. Som person tager du ansvar og finder løsninger, selv i pressede situationer, og sikrer samtidig involvering og ejerskab blandt dine kollegaer. Som person er du positiv og løsningsorienteret, og 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 det er vigtigt at du har sans for detaljerne, 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. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen så kontakt Morten Kring på +45 3075 2694.

Ansøgningsfrist
15. juli 2013

Production Planner

• Supply Chain & Logistics
• Danmark - Kalundborg

Vil du gribe muligheden for at planlægge produktion af insulinprodukter til levering i hele verden?

Vil du være en del af en spændende hverdag, hvor flow, masterdata, ordrebehandling og kommunikation på dansk og engelsk er obligatorisk? Så er dette din chance for at være en del af en spændende organisation!

Om afdelingen
Teamet består af i alt 10 medarbejdere, der varetager forskellige opgaver på tværs af færdigvareproduktionen. Du vil som Produktionsplanlægger indgå som medarbejder i et dynamisk team, der hver dag sikrer, at produktionskapaciteten afbalanceres med efterspørgslen på markedet, samt at flowet i produktionen bevares. Du bliver en del af det logistiske team - et støttende og samarbejdsvilligt team med ansvar for produktionsplanlægning af ca. 10 separate produktionsenheder.

Jobbet
Du vil være ansvarlig for at opfylde kundernes færdigvareordrer og sikre en fremragende leveringsevne til vores datterselskaber og eksterne kunder. Din primære opgave er at planlægge produktionen og udover dit primære produktionsplanlægningsansvar, vil du også være en drivkraft for LEAN procesoptimerings projekter inden for din funktion og sikre, at dit team når de centrale resultatmål.Selvom din arbejdsplads vil være i Kalundborg, vil du få en bred kontaktflade med organisationen lige fra produktionen, QA, Supply Chain Planning, shipping og Customerservice og Novo Nordisks associerede selskaber rundt om i verden.

Kvalifikationer
Det er et krav, at du har en akademisk baggrund – såsom logistikingeniør, produktionsingeniør, (HD) Supply Chain Management eller lignende. Du kan være nyuddannet eller have et par års erfaring fra en lignende stilling, men det vigtigste er, at du har en god forretningsforståelse, stærke analytiske evner og er superbruger i Excel, samt kendskab til SAP vil være en fordel. Vi søger en person, der brænder for at levere resultater af høj kvalitet gennem en struktureret tilgang til de opgaver der vil komme. Du handler proaktivt og er ikke bange for at udfordre det eksisterende, når du ser en mulighed for forbedring.

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
Spørgsmål kan rettes til Jesper Trebbien Andersen på +45 30 75 6776.

Ansøgningsfrist
16. juni 2013

Kemiker

• Kvalitetssikring
• Danmark - Hillerød

Brænder du for at være tæt på pulsen fra produktionen? Så er arbejdet som Kemiker i Novo Nordisks Quality Control Chemistry laboratorium i Hillerød måske noget for dig.

Om afdelingen
Afdelingen udfører kemiske analyser for færdigvareproduktion i Danmark og vores internationale fabrikker. Quality Control Chemistry består af 42 engagerede og dygtige medarbejdere fordelt på kemikere, operatører og laboranter. Afdelingen som er fordelt på to teams, løfter en bred vifte af opgaver lige fra frigivelsesanalyser af aseptiske insulinprodukter til manuelle analyser af færdigvarer.

Jobbet
Du vil skulle beskæftige dig med den daglige drift omkring vores HPLC analyser hvilket bl.a. indebærer fokus på kontrolanalyser, systematisk problemløsning og afvigelseshåndtering. Stillingen giver gode muligheder for at sætte retning og systematik for problemløsning af afdelingens ca. 20 HPLC metoder. Du vil være sparringspartner for afdelingens laboranter.

I afdelingen er der stort fokus på at servicere produktionen med analysetekniske kompetencer, hvilket er en naturlig del af optimeringsarbejdet i produktionen. Du vil spille en central rolle i at håndtere og medvirke til effektiv problemløsning og skabe løsninger af afdelingens out of specifications (OOS’er) og afvigelser. Du vil også indgå i samarbejde med vores supportlaboratorium, som sikrer at rammeforskrifter og metodeoverførsler er egnede.

Kvalifikationer
Du har en videregående uddannelse som kemiingeniør, farmaceut, kemiker eller lignende. Måske kommer du fra en tilsvarende stilling og kender allerede processerne i et QC laboratorium. Erfaring inden fra et eller flere af følgende områder er en absolut fordel: HPLC-analyser, indkøb og kvalificering af laboratorieudstyr, SOP skrivning, systematisk problemløsning, afvigelseshåndtering samt GMP og audits/inspektioner.

Dagligdagen i laboratoriet er præget af et højt tempo, og som person er du fleksibel i forhold til prioriteringer og evnerat træffe de nødvendige beslutninger, også når det går stærkt. Uanset erfaring arbejder du selvstændigt, besidder gode samarbejdsevner og kan prioritere egne opgaver samt følge dem til dørs. Du evner at sætte dig ind i nye områder og have flere bolde i luften uden at miste overblikket. Du er engageret i det du gør, har ambitioner og værdsætter en uformel omgangstone. Da vi arbejder i et internationalt miljø skal du beherske engelsk i både tale og skrift.

Vi kan tilbyde dig en yderst spændende og udfordrende stilling i et dynamisk team, hvor to dage aldrig er ens og hvor du har rig mulighed for selv at præge din arbejdsdag. Der er et højt fagligt niveau i teamet og et tæt samarbejde blandt afdelingens kemikere.

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 Mette Ellemann-Søtofte på +45 3079 4161 eller Lene Søberg Christensen på +45 3079 8604

Ansøgningsfrist
12. juni 2013

Distributions og legaliseringsmedarbejder

• Administration
• Danmark - Bagsværd

Har du lyst til at være med til at sikre kvaliteten af Novo Nordisk’s produkter? Så er du måske den nye Distributions og Legaliseringsmedarbejder i Facility Management Services.

Om afdelingen
Afdelingen er en del af Facility Management organisationen, der driver de kontrakter Novo Nordisk har med eksterne leverandører af rengøring, catering, arbejdsbeklædning og logistik. Desuden varetager vi selv legalisering og som en ny opgave, kørsel af prøver. Du vil blive en del af en afdeling med 15 erfarne og kompetente kollegaer, der har ansvarsbevidsthed, kundeorientering og kvalitet som pejlemærker.

Jobbet
Det primære i dit job bliver at hente prøver fra udenlandske varer på lagre i Københavnsområdet og køre dem til analyse på Novo Nordisks laboratorier i Måløv og Hillerød. Formålet er at sikre, at forsendelserne har det korrekte indhold og lever op til de europæiske krav. En anden af dine opgaver bliver at aflæse varernes temperaturer og indscanne resultaterne elektronisk.

Du vil indgå som en del af det nuværende distributions og legaliserings team. I bliver et team på tre, der skal kunne afløse hinanden, og du vil derfor også blive lært op i opgaverne med legalisering af dokumenter på ambassader og hos myndigheder.

Novo Nordisk stiller bil til rådighed i arbejdstiden. Stillingen er tidsbegrænset frem til 01.03.2015.

Kvalifikationer
Du arbejder struktureret og forstår, at alle detaljer er væsentlige i dette job, da der er tale om livsvigtige lægemiddelprodukter. Det er et vigtigt aspekt af jobbet, at du er i stand til at overholde regler, procedurer og tidsplaner, og at du tjekker selv den mindste detalje, inden du afleverer dine prøver. Det er et krav, at du har erfaring og flair for IT, samt at du kan læse, tale og forstå engelsk.

Du kan f.eks. have fået din indsigt og faglige stolthed fra et job i medicinal eller fødevarebranchen, hvor kvalitet og nøjagtighed er kodeord. Du bruger din positive og imødekommende indstilling til at skabe god kontakt til vores eksterne samarbejdspartnere, og dit gode humør smitter af på dine omgivelser.

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 Jan Løwe-Madsen på +45 3079 7582.

Ansøgningsfrist
27. maj 2013

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 de 2 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 CSP i Måløv sammen med 55 kollegaer, der er delt i 3 teams (Packaging, Process Support og Shipping). CSP 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 de overordnede mål om at levere den rette kvalitet, i rette mængde og til tiden – dette er af afgørende betydning for at sikre effektiv udvikling af Novo Nordisk produkter. Afdelingen er i konstant udvikling med mange spændende udfordringer.

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 og/eller print af etiketter.Du vil indgå i et team med meget dedikerede medarbejdere, og som består af 2 pakkeriteknikere, 2 håndværkere, 1 planlægger, 1 administrativ og 15 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 klargøring til produktion (print af etiketter), 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 udgangen af 2014.

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.

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
For yderligere information, venligst kontakt afdelingsleder Malene Gundestrup på +45 3075 9703.

Ansøgningsfrist
17. juni 2013

QC Laborant

• Kvalitetssikring
• Danmark - Hillerød

Vil du være med på holdet af ca. 44 engagerede medarbejdere i det kemiske analyselaboratorium i QCC SDK i Hillerød?

Om afdelingen
Vi udfører frigivelsesanalyser for Insulin produktionen i Bagsværd, Hillerød, Kalundborg og på prøver fra kontrakt og licensproducenter. Den ledige stilling er i ét af afdelingens to teams bestående af 16 laboranter, 1 elev og en teamleder.

Teamet udfører kemiske frigivelsesanalyser primært HPLC analyser, men også manuelle analyser på insulin færdigvarer. De daglige opgaver består derudover af review 2. kontrol af analyser, udarbejdelse af instruktioner, kvalificeringsdokumentation, analyseansvar og apparatansvar.

Vi er et team, som arbejder målrettet og engageret. Vi har det sjovt og kan lide at gå på arbejde og sætter en ære i at udføre kvalitetsarbejde i et hurtigt tempo.

Jobbet
Vi er en del af en afdeling, som står over for mange udfordrende og spændende opgaver, som stiller store krav til vores samarbejdsevne og forandringsparathed. Der stilles store krav til os om at levere frigivelsesanalyser til tiden og arbejde i flow med samme takt som produktionen. Vi arbejder ligeledes meget med cLEAN kultur i laboratoriet og har fokus på målstyring og løbende forbedring af vores arbejde.

Kvalifikationer
Vi søger en engageret og dynamisk laborant/laboratorietekniker, som er i besiddelse af godt humør. Det er vigtigt, at du har erfaring med både udførsel af analyser, HPLC udstyr og de administrative opgaver, der er i et QC laboratorium.

Du skal have kendskab til GMP og har du erfaring med at være ”på” ved inspektioner, er det en fordel. Gode mundtlige og skriftlige dansk og engelsk kundskaber er ligeledes vigtige arbejdsredskaber. Derudover er det vigtigt, at du er god til at samarbejde omkring løsning af opgaver og samtidig er i stand til at løse opgaver selvstændigt til aftalt tid. Fremtiden byder på store udfordringer i laboratoriet, derfor skal du være klar til forandringer og til at bidrage med forbedrende forslag til arbejdsgange.

Som person skal du have drivkraft, være fleksibel og initiativrig samt tænke innovativt og udvise respekt for det omgivende miljø. Det er vigtigt, at du kan tilegne dig ny viden på en hurtig og effektiv måde. Sidst men ikke mindst er det altafgørende, at du kan lide at udføre analysearbejde.

Vi tilbyder et job fyldt med spændende QC opgaver med god mulighed for udvikling inden for det kvalitetsmæssige fagområde. Derudover kan du forvente en høj grad af selvstændighed og indflydelse på eget arbejde. Der er derfor masser af muligheder for at udvikle både personlige og faglige kompetencer for den rette engagerede person.

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 Freddy Foskjær på + 45 3075 1350 eller Anders Dyrby på + 45 3075 3637.

Ansøgningsfrist
4. juni 2013

Kemiker til miljømonitorering i aseptisk produktion

• Produktion
• Danmark - Gentofte

Kan du lide at gøre en forskel, og har du lyst til at arbejde med miljømonitorering i aseptisk produktion? Så grib muligheden for at indgå i en dynamisk hverdag med gode udviklingsmuligheder og en stor kontaktflade.

Om afdelingen
Biopharm Filling HAA er en højteknologisk fyldefabrik i Gentofte. Vi producerer Glucagon i vials et lægemiddel, der benyttes mod hypoglykæmi. Fyldningen består af følgende færdigvareprocesser: vask og sterilisering af udstyr, formulering, sterilfiltrering, steril påfyldning i isolator, frysetørring, visuel inspektion og miljømonitorering. Til vores procesteam, der består af 13 kemikere og 3 teknikere, søger vi en kemiker/mikrobiolog med blik for kvalitet og produktion til at indgå i den daglige support og monitorering af afdelingens hygiejneniveau i de klassificerede og kontrollerede områder.

Jobbet
Dit ansvar bliver at supportere den daglige produktion i fabrikken inden for hygiejne/miljø monitorering. Det daglige arbejde består typisk i at optimere arbejdsgange, rådgive og træne i korrekt adfærd på klassificeret og kontrolleret område og sikre kontinuerlig forbedring af arbejdsinstruktioner. Derudover er det dit job at vurdere trenddata ifm. produktion af vores lægemidler og dermed sikre, at vi altid holder det høje kvalitetsniveau, der kendetegner Novo Nordisk. Du har derfor løbende konstruktiv dialog med dine kolleger og produktionen om, hvordan vi sikrer kvaliteten, forbedrer vores arbejdsmetoder og undgår fejl. Når vi har udfordringer med kimoverskridelser i processen, har du overblikket, tager initiativ og involverer dine kolleger, så udfordringerne løses hurtigt og effektivt.

Kvalifikationer
Du er evt. nyuddannet civilingeniør i kemi/bioteknologi, farmaceut, biolog eller lignende med et godt resultat. Det er et plus, men ikke et krav, hvis du har erfaring med GMP, fremstilling af lægemidler og myndighedskrav til den farmaceutiske industri. Det er derimod vigtigt, at du trives i en hverdag med hovedvægten lagt på dokumentations- og databearbejdning til trendrapportering blandet med akutte udfordringer. Du kan lide at arbejde koncentreret med data, er kendt for at være struktureret og analytisk, og du har tidligere vist, at du kan sammenholde og gennemskue mange data. Du er god til at prioritere dine opgaver og trives i et dynamisk og til tider uforudsigeligt produktionsmiljø. Engagementet hos dig er tydeligt, både når det gælder håndtering af gentagne kendte arbejdsprocesser, og når du står overfor en ny og ukendt udfordring.

Som person er du energisk og arbejder godt i samspil med andre. Gode kommunikations og samarbejdsevner er vigtige, da du skal arbejde tværgående i produktionen og tvær organisatorisk i afdelingen for at løse opgaverne. Du er desuden god til at skabe en positiv stemning og har en høj grad af ansvars og kvalitetsbevidsthed. Vi tilbyder til gengæld et spændende introforløb og udfordrende job i et team med et højt fagligt niveau.

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 Peter Thomas Olesen på +45 3075 0187

Ansøgningsfrist
9. juni 2013

Teknikervikar

• Produktion
• Danmark - Hillerød

Til Biopharm API Mammalian Cell Produktion, Hillerød, søges en engageret og dynamisk procestekniker med flair for både anlæg og papir.

Faciliteten er etableret i 2007 med henblik på dyrkning og grovrensning af proteiner fra mammale celler til brug ved kliniske forsøg.

Om afdelingen
Afdelingen består af ca 60 ansatte og producerer et hæmofiliprodukt til klinik forsøg. Vi er i gang med flere parallelle projekter for at udvide produktions kapaciteten og for at forberede proces og facilitet til markeds produktion og FDA inspektion.

Vi tilbyder et spændende og afvekslende job i et åbent og dynamisk arbejdsmiljø med rige muligheder for faglig og personlig udvikling.

Jobbet
Du skal primært arbejde med opformering af celler under aseptiske forhold i vores podelaboratorium til produktionen og i den forbindelse også udføre miljømonitorering og in-proces analyser. Vi lægger vægt på at have et driftsikkert podelaboratorium, som altid har podekultur parat, når der er brug for det. Det betyder, at det er vigtigt, at du kan arbejde stabilt og sikkert under aseptiske forhold.

Udover arbejdet i podelaboratoriet er der også opgaver med forskellige in-proces analyser under produktionsforløbet f.eks. pH-måling, celletælling, måling af metabolitter og prøveforberedelse til andre analyser. Af andre opgaver kan nævnes vedligehold og kalibrering af analyseudstyr, udarbejdelse/opdatering af instruktioner og andet dokumentationsarbejde. Vores krav til dokumentation er højt, så dette vil være en væsentlig del af dit arbejde.

Kvalifikationer
Du er uddannet laborant, laboratorietekniker, levnedsmiddeltekniker, mejeritekniker eller lignende og har erfaring med celledyrknings eller fermenteringsprocesser samt fortrolighed med arbejde under aseptiske forhold.

Du har evner for såvel det praktiske arbejde i anlægget, samt for skriftlig rapportering, og ser muligheder i at kunne kombinere omhyggelighed og faglig kunnen med de biologiske aspekter af celledyrkningen som et spændende arbejdsområde.

Da arbejdet foregår i tværfaglige grupper, er det vigtigt, at du har lyst og evner både til at arbejde selvstændigt og til at samarbejde på tværs i afdelingen. Forståelse, interesse for og erfaring med kvalitetssystemer (GMP/ISO) vil være en fordel, da kvalitetsarbejdet er en vigtig del af vores hverdag. Vi lægger desuden vægt på, at du har et godt humør, er teamplayer, og kan lide at tage fat i opgaverne, også når de ikke bliver lagt tilrette foran dig. Du skal kunne håndtere flere opgaver på samme tid og bevare overblikket i pressede situationer. Fortrolighed med IT systemer er nødvendigt, da faciliteten er automatiseret.

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 Hanne Tøttrup +45 3079 1858 eller Mikael Frederiksen +45 3079 8652.

Ansøgningsfrist
27. maj 2013.

Processuporter akademiker

• Produktion
• Danmark - Hillerød

Processupport akademiker med flair for produktionsoptimering og kvalitet

Kunne du tænke dig at blive en del af et hold engagerede og resultatorienteret ingeniører og specialteknikkere, som sigter efter at nå den bedste performance på vores montage & pakke linjer?

Om afdelingen
Site Danmark Finished Products i Hillerød er en stor fuldautomatiseret montage og pakkesite. Vi monterer & pakker engangspennene FlexPen og FlexTouch.

Jobbet
Du vil indgå i FlexPen processupport teamet, hvor du vil få ansvaret for at supportere vores højvolumen og fuldautomatiske FlexPen pakkelinie. Du vil opleve, at du selvstændigt kan lede projekter, drive den teknologiske udvikling og de mange igangværende optimeringsopgaver på udstyret. I forbindelse med de løbende forbedringer vil du ligeledes få ansvaret for at dokumentere, at kvaliteten opretholdes.

I tæt samarbejde med teamkolleger og andre afdelinger i området, vil du arbejde aktivt med at sikrer, at produktion og processer har de bedste forudsætninger for at leve op til gældende kvalitets og cGMP krav. Du vil arbejde med at dokumentere, at kvaliteten er ok, hvis vores processer mod forventning ikke følger standarden. Når dette sker, venter et større eller mindre opklaringsarbejde, for at identificere, hvilken proces der har fejlet, hvorfor den har fejlet, og hvordan det undgås at fejlen sker igen.

Du vil opleve, at vi fokuserer meget på LEAN ved f.eks. at anvende værktøjer til problemløsning, arbejde efter standarder samt anvende standardiserede principper i vores ledelse af dagligdagen.

Som supporter har du en stor kontaktflade og skal samarbejde med forskellige faggrupper både internt og eksternt i afdelingen. Det giver en udfordrende og alsidig navigation mellem disse, når opgaver skal løses.

På sigt kan der forekomme begrænset rejseaktivitet på produktionssites i udlandet og du vil ligeledes kunne komme til at arbejde med at udføre valideringsopgaver. Du får rig mulighed for selv at strukturere og planlægge din hverdag.

Kvalifikationer
Du har en baggrund som ingeniør eller lignende. Da teamet står overfor at skulle udvides kraftigt, er der plads til såvel nyuddannede som kandidater med lang erhvervserfaring.

Erfaring indenfor færdigvareproduktion af medicinalprodukter og kendskab til cGMP er en klar fordel. Ligeledes vil teknisk og automatik erfaring være en fordel. Der vil blive lagt vægt på, at du har erfaring med selvstændigt at drive opgaver, projekter og optimere produktionen. Du har en skarp analytisk sans, der sammen med dine Lean erfaringer sikrer, at du naturligt indgår i vores eksisterende forbedringskultur.

Du er hurtig til at få overblikket over komplekse processer eller problemstillinger og løser dem på en systematisk måde. Dit arbejde er i høj kvalitet, og du motiveres af at vise resultater og lukke dine opgaver til tiden. Du har endvidere den egenskab at kunne arbejde selvstændigt med svære opgaver og samtidig være en teamplayer, der gerne yder en ekstra indsats for holdet. Det er afgørende, at du er en person der går forrest og selv tager initiativ til at løse udfordringer. Dit gode humør og evnen til at skabe gode relationer sikrer, at du lykkes med dine opgaver på en god måde. Du er åben og ærlig, giver dine meninger til kende og er i stand til at give og modtage konstruktive feedback.

Du bliver en del af en spændende arbejdsplads med udfordringer, udviklingsmuligheder, engagerede kollegaer og høje krav til dig som supporter. Vi kan tilbyde et job, hvor ingen dage er ens, og hvor du har rigtig gode muligheder for at udvikle dine kompetencer.

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 Janni Nielsen på 3079 7276

Ansøgningsfrist
02. juni 2013

Operatør til Natrengøring

• Produktions operatør
• Danmark - Gentofte

Vil du være med til at sikre, at vores produktionsmiljø lever op til vores høje standarder, hvor kvalitet og fokus på detaljen er altafgørende? Er du ansvarsbevidst og stabil? Og kan du forestille dig at arbejde, når de fleste har fri?

Så er du måske den nye kollega, vi søger i natrengøringen, i Gentofte.

Afdelingen er en stor aseptisk fyldeafdeling med ca. 200 medarbejdere. Produktionen omfatter præparation, sterilfiltrering, fyldning, frysetørring, autoklavering og inspektion.

Vikariatet løber frem til 31. december 2013.

Fælles ansvar og udfordringer
Du vil indgå i et team bestående af 9 personer som i fællesskab er ansvarlige for rengøringen i produktionsområdet i aften og nattetimerne.

Arbejdet består af produktionsrengøring i en steril afdeling. Der arbejdes efter arbejdsinstruktioner, og rengøringskvaliteten er af stor betydning for produkterne i afdelingen. I arbejdet indgår også et ansvar for at tilrettelægge og løse opgaverne i fællesskab, sammen med resten af teamet. Som en del af dit arbejde deltager du i kurser og intern undervisning, der er obligatorisk for stillingen.

Arbejdstiden er fra mandag til fredag fra kl. 22.00 til 06.00

Stabil og ansvarsbevidst
Du har gerne produktionserfaring eller erfaring inden for rengøringsbranchen. Det vigtigste er dog, at du tager ansvar og er meget bevidst om kvaliteten i dit arbejde.

I vores team er samarbejde vigtigt, så du skal have en positiv indstilling og lysten til at løse opgaver i fællesskab med kolleger. Du er stabil og klar til at tage fat, også når arbejdet er fysisk hårdt. Det er vigtigt, at du kan holde hovedet koldt i en travl hverdag.

Du skal også tage stilling til den udfordring det er at arbejde om natten frem for om dagen.

Du har som minimum 9. klasses afgangseksamen med minimumskarakteren 7 i dansk og matematik (8 på gl. karakterskala) samt 4 i engelsk (7 på gl. skala). Vi beder dig vedhæfte dokumentation for uddannelse og karakterer, når du ansøger. Desuden regner vi med, at du har flair for teknik og IT.

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 Pernille Thrue på +45 3079 8301.

Ansøgningsfrist
26. maj 2013.

Produktionskemiker

• Produktion
• Danmark - Kalundborg

Har du en god forståelse for sammenhængen mellem processer og produktionsudstyr, så har du mulighed for at få et spændende kemikerjob på højt niveau. Du kan glæde dig til at få stor indflydelse på dine egne opgaver, der spænder vidt fra drift til komplekse valideringsopgaver.

Om afdelingen
Du bliver en del af support team, der består af teknikere og kemikere. Du og dine kolleger har ansvar for den primære proces i forbindelse med grovrensning af diabetesprodukter samt for det tilhørende udstyr. Vi yder support, løser problemer, optimerer og validerer. Samtidig sikrer vi, at processer, udstyr og produktkvalitet lever op til myndighedernes krav/forventninger, og at dette er veldokumenteret. Vi bruger LEAN som vores vigtigste styringsværktøj.

Jobbet
Du får selvstændigt ansvar for en række opgaver i spændet mellem anlæg og processer. Du yder support til operatørerne, så driften kører stabilt. Er der problemer, løser du disse på en systematisk måde med brug af data og de nyeste LEAN værktøjer. Du kommer også til at udarbejde instruktioner, reviews og anden dokumentation. Derudover kommer du til at bringe dine evner i spil i komplekse validerings og rapporteringsopgaver. På tværs af dine opgaver sparrer du med dine dygtige og engagerede kolleger, så vi får delt viden og sikret, at alle udvikler sig fagligt og personligt.

Kvalifikationer
Du har en naturvidenskabelig uddannelse som f.eks. ingeniør, farmaceut, cand.scient. eller lignende. Via dine hidtidige job har du fået en god forståelse for sammenhængen mellem processer og udstyr samt kendskab til GMP og/eller andre kvalitetssystemer. IT er en naturlig del af dit arbejde, og du har generelt teknisk flair. Som person er du kendt for dit engagement, din positive indstilling samt din kvalitets og ansvarsbevidsthed uanset om du arbejder alene eller i team eller med andre kemikere eller operatører. Dit overblik gør, at du trives med at have mange sideløbende opgaver, også når der travlt. Du kan lide at udvikle ting til det bedre, og derfor møder du forandringer i processer, organisation og systemer med åbent sind.

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.

Novo Nordisk i Kalundborg

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.

Kontakt
Vil du vide mere om stillingen, så kontakt Birgitte Krog Christensen på +45 3075 6175.

Ansøgningsfrist
31. maj 2013

Kvalitetskoordinator

• Forskning og Udvikling
• Danmark - Måløv

CS Aseptic Pilot Plant udvider, og søger derfor snarest en kvalitetskoordinator. Aseptic Pilot Plant er en mindre produktionsenhed i Gentofte og Måløv, som blandt andet fremstiller præparater til kliniske undersøgelser. Afdelingen er en del af R&D CMC Clinical Supplies.

Om afdelingen
Vi befinder os i grænsefladen mellem udvikling og produktion og har bred kontakt til mange funktioner i virksomheden. Vores primære opgave er at producere aseptisk fremstillede færdigvarer til brug i prækliniske og kliniske studier i forbindelse med virksomhedens udviklingsprojekter. Produkterne er derfor skiftende – ofte nye – og produceres efter gældende cGMP regler. Vi har en travl hverdag og samtidig lysten og viljen til cLEAN arbejde.

Jobbet
Dit fokus vil være at sikre, at afdelingen efterlever de gældende kvalitetskrav. Du vil være ansvarlig for afdelingens kvalitetssystem og for at fastlægge kvalitetsmålene. Du vil skulle udtænke planer/strategier og implementere disse, så målene nås. Du vil være sparringspartner for afdelingens ledelsesgruppe og vil være faglig ekspert for en række af afdelingens kvalitetsprocesser, herunder afdelingens NC-ekspert og CR-ekspert. Du vil skulle forestå relevant træning samt medvirke til en god dialog med afdelingens medarbejdere om kvalitetsarbejdet og målene, herunder om medarbejderne bidrager i at sikre opfyldelse af målene. Du vil være ansvarlig for interne audits og myndighedsinspektioner. Du kan forvente at skulle løse både praktiske og dokumentationsmæssige opgaver herunder udarbejdelse af afvigelser, ændringssager, valideringsdokumenter og instruktioner.

Kvalifikationer
Din uddannelsesmæssige baggrund er en videregående naturvidenskabelig uddannelse, f.eks. kemi ingeniør eller farmaceut. Det vil være en fordel, hvis du tidligere har arbejdet med GMP i et produktionsmiljø eller har en baggrund i QA. Du er god til at formidle mål og planer. Du har nemt ved at samarbejde og skabe gode relationer til kollegaer. Du er vant til at arbejde selvstændigt, tage initiativ og give en klar retning for arbejdet. Du formår at holde overblikket og fortsat arbejde omhyggeligt med dine opgaver.

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 Lise Ramsgaard Jensen på +45 3075 3721.

Ansøgningsfrist
6. juni 2013

Rensningsteknikere

• Forskning og Udvikling
• Danmark - Bagsværd

Til CMC API Development, Downstream Pilot Plants, bygning 1T i Bagsværd søger vi 3 selvstændige og dygtige teknikere med flair for både anlæg og papirarbejde.

Om afdelingen
I 1T oprenser vi proteiner til brug i kliniske studier. De ledige stillinger er i et team på 7 teknikere, 2 kemikere og 1 teamleder, som sammen løser en række opgaver i forbindelse med drift og gennemførelse af kampagner i Multikolonne anlægget. Teamet er en del af en større afdeling med ca. 70 ansatte fordelt i 4 oprensningspilotanlæg på tværs af Bagsværd og Gentofte. En vigtig egenskab for både anlæg og medarbejdere er fleksibilitet, da anlæggene håndterer forskellige processer og proteiner.

Vi tilbyder et spændende og afvekslende job i et åbent og dynamisk arbejdsmiljø med god mulighed for faglig og personlig udvikling. Stillingerne indebærer dagvagter, eftermiddag/aftenvagter samt weekendarbejde.

Jobbet
Arbejdsopgaverne vil være relateret til procesafviklingen i anlægget med fokus på præparativ oprensning og dertil hørende dokumentation. Du vil også skulle deltage i andre af teamets opgaver i forbindelse med løbende kontrol af bl.a. udstyr og råvarer. Vores arbejde udføres og dokumenteres i henhold til GMP, og der forventes en systematisk tilgang til tingene.

Herudover skal du også varetage opgaver, der styrker afdelingens drift og udvikling. I afdelingen arbejder vi med LEAN og stræber efter hele tiden at forenkle vores arbejdsprocesser, og dit input vil være værdifuldt for at vi løbende kan forbedre vores procedurer og reducere overflødige rutiner.

Kvalifikationer
Du er uddannet kemotekniker, procesteknolog, levnedsmiddeltekniker eller lignende, og har gerne praktisk oprensningserfaring i laboratorie-/pilotskala eller fra produktion. Du har erfaring med eller interesse og flair for proces kontrolsystemer (Sattline og Unicorn). Du har teknisk interesse og viden om procesteknik og processtyring. Kendskab til søjlekromatografi og arbejde efter GMP vil være en fordel. Du har evner for såvel det praktiske arbejde i anlægget, samt for udarbejdelse af dokumenter.

Evne til samarbejde og kommunikation er en nødvendighed, da opgaverne bliver løst i fællesskab. Vi lægger desuden 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. Du skal kunne håndtere flere opgaver på samme tid og bevare overblikket i pressede situationer.

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 Bente Vejby Jensen på +45 3079 1308 eller Charlotte le Fevre på +45 3075 1148

Ansøgningsfrist
7. juni 2013

Laborant

• Produktion
• Danmark - Kalundborg

Har du lyst til at være med til at sikre at kvaliteten af vores produkter er helt i top og er du drevet af trangen til at få det bedste resultat ud af komplicerede kemiske analyser? Så er denne stilling som laborant i Novo Nordisk, Biopharm QC Kalundborg måske noget for dig.

Om afdelingen
Biopharm QC Ka søger erfaren og fleksibel laborant til en fast stilling i vores HPLC/VAnd team. Afdelingen varetager mikrobiologiske, kemiske og immunologiske analyser fra produktionen af blødermedicinen NovoSeven (Faktor VII). Afdelingen er i rivende udvikling og står overfor en udvidelse i forbindelse med analyse af miljø og vandprøver fra en ny fyldefabrik.

Afdelingen består af 45 engagerede medarbejdere, fordelt i tre analyseteams. HPLC/VAND teamet består af 9 laboranter, fire kemikere og en teamleder.

Jobbet
Som laborant i teamet skal du være med til at sikre den daglige drift, fra analyse til resultatfrigivelse af både produktions og stabilitetsprøver. Analyserne består primært af HPLC/vand analyser. Der må derfor påregnes en del databehandling herunder manuel integration.

Af andre arbejdsopgaver, kan bl.a. nævnes apparatkontrol, vedligeholdelse og troubleshooting på diverse udstyr, samt foretage årskontrol af udstyr. Endvidere skal du påregne at være med til at udarbejde analyseforskrifter, instruktioner, NC og CR sager.

Kvalifikationer
Du er uddannet laborant med erfaring i at arbejde efter høje kvalitetskrav, GMP og LEAN. Det er en forudsætning for en ansættelse, at du har erfaring med HPLC-analyser eller vand analyser. Yderligere er det et krav, at du kan anvende Empower software. Det er en fordel, at du er fortrolig med LIMS systemer og software der kan overføre data fra HPLC til LIMS, eks. LIMSLink og stockmodul.

En af dine styrker kunne være din analytiske evne til at kunne udføre troubleshooting på HPLC udstyr, baseret på dit indgående kendskab til udstyrets funktionalitet. Du er nok allerede nu i dit nuværende team kendt som en systematisk problemløser med flair for optimering.

Arbejdsmæssigt forventes det at du er fagligt dygtig og vant til at følge en driftsarbejdsplan. Du skal være omstillingsparat og selv bidrage til prioriteringer, da opgaver i løbet af dagen kan blive ændret. Som person forventes det, at du er en aktiv teamplayer med initiativ og med en god portion humor.

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 Skipper +45 3079 9663.

Ansøgningsfrist
27. maj 2013.

Team leder

• Produktion, Teamleder
• Danmark - Kalundborg

Er du en teamleder med holdninger? Har du et helhedsorienteret menneskesyn? Og vil du være med til at skabe et lederteam, der er drevet af resultater, Quality Mindset og menneskelige værdier? Så er jobbet som teamleder i afdeling 055 noget for dig.

I Biopharm API Production arbejder vi dedikeret på at producere kvalitetsprodukter til behandlingen af hæmofili. Afdeling 055 søger teamledere, der vil være med til at løfte vores ambition om at hjælpe mennesker med hæmofili til at leve det liv, de ønsker. Vi er ved at udbygge vores lederteam og søger erfarne teamledere, der brænder for at skabe effektive og stabile processer gennem en stærk cLEAN kultur. Denne rejse kan du få afgørende indflydelse på og jobbet er derfor velegnet til den erfarne teamleder, der gerne vil have erfaring med opbygning af ledelseskultur. Måske fordi du har ambitioner om afdelingsledelse senere i karrieren. Du vil referere til en meget erfaren afdelingsleder, der vil være en stor støtte for dig i din personlige og faglige udvikling.

Om afdelingen
Afdelingen består i dag af knapt 100 medarbejdere, fordelt på 6 teams som producerer blødermedicin NovoSeven®. Vi producerer hver dag og nat hele året rundt.

Vi søger en teamleder til Udstyrsteamet bestående af 20 ingeniører, smede og teknikere samt en teamleder til Produktionsteamet bestående af 20 operatører. Du vil blive ansvarlig for den daglige ledelse i et team, hvor du skal sætte retning, udvikle medarbejderne og facilitere en problemløsningskultur. Afdelingen har været gennem PS@shopfloor og en af dine opgaver er, at videreudvikle kulturen på denne basis.

Jobbet
Du indgår som teamleder i et tæt samspil med afdelingens øvrige teamledere, og der lægges stor vægt på at fungere som én samlet produktion med fokus på fælles mål og tværgående løsninger. Samspillet mellem teamlederne er en vigtig prioritet, og du forventes at kunne bidrage aktivt i en kultur af åbenhed, samarbejde og holdånd.

Du vil som teamleder skulle varetage en udadvendt rolle, der i kraft af sin placering i produktionen har organisationens bevågenhed. Din indsats som teamleder gør en væsentlig forretningsmæssig forskel, og du kan se frem til en hverdag i et foranderligt miljø, hvor tempoet er højt, og hvor vigtige beslutninger skal træffes i spændingsfeltet mellem mange interessenter.

Kvalifikationer
Du forventes at være analytisk stærk og have flere års ledelseserfaring. Du skal kunne motivere og sætte retning sideløbende med at fastholde et stringent performance fokus. Du er entusiastisk, behandler dine kolleger og medarbejdere med respekt samtidig med, at du fokuserer skarpt på indfrielse af dine og afdelingens ambitiøse mål. Opgaverne kræver et godt kendskab til cLEAN som ledelsesværktøj.

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 Jesper Platz på +45 3075 5599.

Ansøgningsfrist
1. juni 2013.

Akademiker

• Forskning og Udvikling
• Danmark - Gentofte

Vil du arbejde i et dynamisk og foranderligt miljø og mærke ”pulsen” fra både udvikling og produktion - så har vi lige jobbet til dig. Vi udvider, og søger derfor en erfaren akademiker til Aseptisk Pilot Plant.

Om afdelingen
Afdelingen er en del af R&D CMC Clinical Supplies. Vi befinder os i grænsefladen mellem udvikling og produktion og har bred kontakt til mange funktioner i virksomheden. Vores primære opgave er at opskalere og producere aseptisk fremstillede færdigvarer til brug i kliniske studier i forbindelse med udviklingsprojekter. Hver kampagne, vi producerer, er et nyt produkt med sin egen ny formulering. Det giver en høj kompleksitet ift. produktions-forberedelse. Aseptisk Pilot Plant består af 55 medarbejdere i henholdsvis Gentofte og Måløv.

Jobbet
Arbejdet kræver en stærk faglig indsigt indenfor aseptisk produktion og evnen til at implementere nye tiltag og forbedringer i samarbejde med flere interessenter. Erfaring og viden indenfor inspektion af færdigvare vil være en fordel. Herudover indebærer arbejdet deltagelse i udviklingsprojekterne i form af koordinering med produktets projektledelse vedr. overførsel af produktionsprocesserne fra laboratorieskala til pilotskala samt videre overførsel til virksomhedens produktionsafdelinger. Du vil blive den faglige ansvarlig for compliance og LEAN processer indenfor dit fagområde, og du skal varetage udarbejdelse af procedurer, afvigelser og review af dokumentation fra produktionerne i samarbejde med øvrige kolleger i teamet.

Kvalifikationer
Vi forventer, at du er uddannet farmaceut, kemiingeniør, eller lign. uddannelse. Det er en klar fordel hvis du har specifik erfaring med aseptisk produktion i den farmaceutiske branche eller stor erfaring med projektledelse indenfor udvikling af lægemidler.

Vi leder efter en kollega med godt humør og som med initiativ, selvstændighed og ansvar tager fat på nye opgaver. Vi forventer, at du er god til at strukturere og planlægge arbejdet og ikke lader dig slå ud af en omskiftelig hverdag, hvor der løbende skal prioriteres og træffes nye beslutninger. Du formår at holde overblikket og fortsat arbejde omhyggeligt med dine opgaver.

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 Lene Kragelund på +45 3079 3601.

Ansøgningsfrist
1. juni 2013

El og Maskinsikkerheds Koordinator

• Miljø, arbejdsmiljø og sikkerhed
• Danmark - Søborg

Kan du sætte retning og være med til at sikre, at Product Supply’s multi site produktionsmiljø i Danmark overholder gældende standarder og regler indenfor el- og maskinsikkerhed? I så fald har vi et meget spændende og udfordrende job til dig.

Om afdelingen
Du bliver en del af vores Environment, Health & Safety (EHS) afdeling med base i Søborg. Vi er 23 dedikerede specialister, rådgivere og projektledere, der leverer support og rådgivning til organisationen med fokus på opfyldelse af den overordnede EHS-strategi – herunder Novo Nordisk’s særlige fokus på de tredobbelte bundlinje, hvor miljømæssigt ansvar er sidestillet med finansielle resultater og social ansvarlighed. Du bliver afdelingens omdrejningspunkt ift. specifik viden om el- og maskinsikkerhed, CE mærkning etc.

Jobbet
Du skal være den proaktive igangsætter og facilitator, ikke den tekniske ekspert. Du skal bl.a. sørge for, at vi får sat dine fokusområder højt på agendaen i et meget komplekst organisatorisk landskab med mange interessenter. Konkret skal du bl.a. gennemføre analyser samt igangsætte og gennemføre koordinerede tiltag som integreres i Novo Nordisk’s eksisterende systemer. Herunder skal du samle viden fra mange forskellige tekniske eksperter inden for el- og maskinsikkerhed og få deres input koordineret og formidlet på en måde, der skaber fælles forståelse og enighed om det fornuftige og rigtige i tiltagene.

På maskinområdet skal du koordinere udviklingen og implementeringen af systemer, standarder og værktøjer til sikring af maskinsikkerhed, herunder CE-mærkning. På el-området skal du koordinere implementering af Novo Nordisk’s SKS-A system for el-sikkerhed, så virksomheden kan opretholde autorisation til selv at udføre arbejder i henhold til Stærkstrømsbekendtgørelsens afsnit 6.

Kvalifikationer
Du har en teknisk uddannelse som ingeniør, maskinmester eller lignende og min. 3 års erfaring fra et job, hvor du har arbejdet med maskin- og el-sikkerhed inkl. koordinering af aktiviteter inden for områderne. Du trives således med selvstændigt at samle viden og koordinere aktiviteter. Det er ikke afgørende, at du har dyb teknisk viden, men du skal have en god grundlæggende forståelse for el- og maskinsikkerhed og tilhørende systemer, så du kan begå dig blandt eksperter – og sikre at du får koblet den rigtige hjælp på, når det er nødvendigt. Det er samtidig helt afgørende, at du er rigtig dygtig til at kommunikere, og at du har du den udadvendte og imødekommende personlighed, der skal til for at skabe, udvikle og drive netværk. Derudover skal du være god til engelsk, skriftligt og mundtligt.

I Novo Nordisk stræber vi efter at være de bedste. Vi er førende i verden indenfor diabetesbehandling og en væsentlig aktør på vores andre forretningsområder. Derfor kan vi tilbyde vores medarbejdere mulighed for en stærk professionel udvikling.

Kontakt
Vil du vide mere om stillingen, så kontakt Tomas Schou Winther på +45 3075 1458

Ansøgningsfrist
29. maj 2013

Laborant

• Produktion
• Danmark - Gentofte

I Biopharm QC Support søger vi en laborant til en spændende stilling med hovedvægt på BIO analyser herunder ELISA og enzymkinetiske analyser samt SDS-PAGE til vores hæmofiliprodukter.Jobbet er lige noget for dig, hvis du har lyst til at lære afdelingens mangeartede opgaver at kende – inden for metodeoverførsel, validering og frigivelse af kliniske fase 3 batche på Biopharm’s hæmofili portofolie.

Om afdelingen
Vi er 74 medarbejdere organiseret i fire analyseteams samt en stabsfunktion, som varetager tværgående aktiviteter.

Jobbet
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, optimering og validering af analysemetoder samt evt. indkøring og kvalificering af nyt udstyr.Du kommer i et team med engagerede kollegaer bestående af en teamleder samt kemikere og laboranter. Du skal samarbejde med kolleger i dit team og på tværs af afdelingen samt være i kontakt med QA, analyseudviklingsafdelinger og Biopharms QC-laboratorier.Vi kan tilbyde dig et udfordrende job med store muligheder for udvikling af dine faglige og personlige kompetencer.

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 kvalitetsbevidsthed. 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, at 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 Ann Cherie Grønbech på +45 3075 8918 eller Anette Lund Kristensen på +45 3075 1947.

Ansøgningsfrist
27. maj 2013

Laboratorieassistent

• Produktion
• Danmark - Kalundborg

Har du lyst til at være laborant i en afdeling med aktiviteter centralt placeret i Novo Nordisk’ insulinproduktion og vil du være med til at sikre, at vores produkter lever op til vores høje kvalitetskrav? Så er du måske vores nye kollega i QC laboratoriet i Insulin Manufacturing II (IM2).

I IM2 produceres udgangsmateriale til humaninsulin- samt en række moderne insulinfærdigvarer, hvilket gør IM2 til et af Novo Nordisks vigtigste områder i insulinproduktionen.

Om afdelingen
Du vil blive en del af et kemisk analyseteam bestående af 30 engagerede og dygtige laboranter og kemikere. Teamet er en del af QC laboratoriet i IM2, hvor der udføres både kemiske og mikrobiologiske analyser af vores produkter i Diabetes API. I afdelingen er vi ca. 80 medarbejdere fordelt i 4 teams.

Jobbet
Som laboratorieassistent i teamet skal du være med til at sikre det daglige flow i laboratoriet i form af modtagelse af prøver og kemikalier. Udføre internt vedligehold i henhold til SAP, samt fremstille eluenter og reagenser til analysebrug. Arbejdet understøtter den daglige drift for hele laboratoriet både i kemisk team og i mikrobiologisk team og du vil få kontakt med mange mennesker. Det er vigtigt, at du kan overskue flere opgaver ad gangen og kan afslutte opgaverne til tiden i høj kvalitet.I afdelingen er der stor fokus på, at levere analysesvar til tiden, overholdelse af vores kvalitetsmål og systematisk opfølgning på analyseproblemer. Du vil som del af teamet, naturligt indgå i dette arbejde.

Kvalifikationer
Du skal have en relevant laboratorieteknisk uddannelse (Laborant). Derudover har du kendskab til LIMS og SAP, samt kendskab til GMP/ISO-reglerne.Du er frem for alt serviceminded, har gode kommunikationsevner og værdsætter respektfuldt og ligeværdigt samarbejde. Vi forventer at du er engageret, udviser høj grad af selvstændighed og har lyst til at medvirke til den fortsatte udvikling af vores positive og lærende kultur. Vi kan tilbyde dig en yderst spændende og udfordrende stilling i et dynamisk team, hvor to dage aldrig er ens og hvor du har rig mulighed for selv at præge din arbejdsdag. Stillingen er tidsbegrænset til 12 mdr.

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 Janne Maibrit Andersen på +45 3079 0304.

Ansøgningsfrist
25. maj 2013

Ansvarlig til intern miljø

• Produktion
• Danmark - Kalundborg

Vil du være med til at sætte retning for et vigtigt område i Novo Nordisks insulinproduktion? Så søg denne spændende og udviklende stilling i vores Grovrensningsfabrik, hvor der produceres udgangsmateriale til en række human- og moderne insulinfærdigvarer, hvilket gør IM2 til et af Novo Nordisks vigtigste områder i insulinproduktionen. Grundet øget efterspørgsel af vores produkter, står vi overfor en meget spændende opgave mht. at udvide og optimere fabrik og processer over de næste år.

Om afdelingen
Vores primære opgaver er at supportere driften hvor processerne bla. er capture, oprensning, krystallisation og centrifugering inkl. utility-anlæg herunder bla. CIP, solventer, procesvand, frostrum og Kill-anlæg. Du kommer til at indgå i et team på ca. 15 dygtige kolleger med varierende baggrund, ansvarsområder samt kompetencer.

Jobbet
Du bliver sammen med en kollega ansvarlig for monitorering af intern miljø, hvilket er en forudsætning for at vi kan producere kontrolleret i vores faciliteter.Du er dagligt i anlægget for at udtage prøver jf. schedulerplaner som du er ansvarlig for er vedligeholdt. Dette kræver at du bliver dus med proces- og produktionsafviklingen, og har et godt samarbejde med operatørerne, laboratoriet og QA.Du tager ansvar og er på forkant ift. at der bliver foretaget nødvendige aktioner ved overskridelser eller stigende trends der bla. identificeres via årsrapporterne, og står i spidsen for en effektiv og systematisk problemløsning samt afvigelseshåndtering. Du vil ligeledes skulle supportere vores finrensningsfabrik i DD ift. afvigelseshåndtering, hvor du trækker din erfaring med mikrobiologien, evner til koordinering og problemknusning.Du vil blive inddraget når der eksempelvis er ombygninger, hvor du skal tage stilling til og sikre at der bliver iværksat de rigtige foranstaltninger og efterfølgende målinger, således at miljøet er i kontrol før produktionsopstart.Du kommer til at indgå i procesgruppen for Enviroment Monitoring på tværs af DAPI, og herunder bliver du ansvarlig for at myndighedskrav tolkes på det rette niveau og bliver implementeret i vores kvalitetssystem i hele IM2.Udover miljømonitorering vil du hjælpe dine kollegaer med øvrige processer vi har ansvaret for, eksempelvis monitorering af vand.

Kvalifikationer
Du har en fortid hvor du har arbejdet med mikrobiologi som enten uddannet akademiker, laborant, tekniker eller lignende, og du har gerne erfaring fra lignende stilling i den pharmaceutiske industri.Du er natur detajleorienteret, utrolig grundig og har et godt håndelag ift. håndtering af prøver. Omvendt formår du også at hive dig op og i helikopteren, og forudse og tage aktion på konsekvenser af ændringer i eksempelvis systemer, analysemetoder og krav.Herudover er en af dine styrker at du arbejder sikkert med data og statistik, bla. i Excel, og kan udarbejde dokumentation af en meget høj kvalitet. Du arbejder struktureret bla. vha. LEAN-værktøjer, har overblik og er på forkant med dine opgaver.Du mestrer engelsk i både skrift og tale, da du skal præsentere miljø på audits. Du er udadvendt og teamplayer, idet din succes bla. afhænger at dit gode samarbejde med øvrige faggrupper.

Novo Nordisk i Kalundborg er en by i byen. Området er på 1.350.000 m2 med eget vejnet, kun godt en times kørsel fra København. Vi er 3.500 mennesker i alt fordelt på 16 fabrikker, og vi producerer bl.a. 50 % af verdens insulin. Vi arbejder helt på forkant af udviklingen inden for teknologi, systemer, metoder og processer. 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 Dorte Rehné på +45 3079 0622.

Ansøgningsfrist
29. maj 2013

Tekniker

• Forskning og Udvikling
• Danmark - Måløv

CS Aseptic Pilot Plant udvider, og søger derfor snarest en erfaren og engageret laborant på fuld tid som præparationsteknikker. Aseptic Pilot Plant er en mindre produktionsenhed i Gentofte og Måløv, som blandt andet fremstiller præparater til kliniske undersøgelser. Afdelingen er en del af R&D CMC Clinical Supplies.

Om afdelingen
Vi befinder os i grænsefladen mellem udvikling og produktion og har bred kontakt til mange funktioner i virksomheden. Vores primære opgave er at producere aseptisk fremstillede færdigvarer til brug i prækliniske og kliniske studier i forbindelse med virksomhedens udviklingsprojekter. Produkterne er derfor skiftende – ofte nye – og produceres efter gældende cGMP regler. Vi har en travl hverdag og samtidig lysten og viljen til cLEAN arbejde. Fleksibilitet er en selvfølgelighed.Afdelingen er i gang med at etablere nye produktionsfaciliteter i Måløv og forventer at flytte dertil inden for det næste år.

Jobbet
Arbejdsopgaver i teamet er blandt andet produktion af lægemidler under aseptiske betingelser, udarbejdelse af produktionsforskrifter, afvigelser og review af dokumentation fra produktionerne i samarbejde med øvrige kolleger i teamet. Derudover har vi udstyrsansvar for præparationsudstyr.

Kvalifikationer
Vi forventer, at du er uddannet laborant. Du har stor praktisk erfaring med præparation af lægemidler under klassificerede forhold, og du vil være i stand til selvstændigt at lave forskrifter. Du har bred viden om cGMP, gode samarbejdsevner og et godt humør. Du kommunikerer åbent og konstruktivt, er initiativrig, fleksibel og ansvarsbevidst. Du skal kunne bevare overblikket over mange opgaver på en gang, i et til tider meget hektisk miljø.

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 Lene Kragelund på +45 3079 3601.

Ansøgningsfrist
1. juni 2013