Senior Validation Professional

Are you skilled within GMP and do you like to work in an exciting project environment? Do you want to be a part of initiatives where quality is a priority? Then we hope that you would like to become our new Project Quality Professional, we are seeking more than one candidate! 

The position
The Project Quality Professional will join the team responsible for the implementation of standardised qualification processes on sites across the world. We are looking for someone with production and validation knowledge, who can take the lead and set the direction based on best practice and broad cooperation with sites. Although the role will be situated in Denmark, it will integrate with the Project organizations at our global sites.

Key responsibilities include:

• Implementation of standardised project quality processes for the Fill & Finish Expansions Project.
• Preparation of standard validation execution setup – using a Science and Risk-based Validation (SRV) approach.
• Communication with counterparts around the world.

Qualifications
To succeed in this role, you should:

• Have a relevant academic education, such as production, chemical or process engineering, pharmacy, biology, microbiology, or equivalent.
• Some experience in the pharmaceutical industry, preferably from working in the production or as QA for production.
• Have experience in qualification or validation of processes/equipment’s.

The ideal candidate for this role should be able to communicate clearly and distinctly in English, both in written and spoken form. They should be known for their excellent collaboration skills and have a purposeful, determined approach to taking the lead on tasks. Additionally, the ideal candidate should enjoy new challenges and be eager to learn new things.

About the department
The Validation Standards department at Novo Nordisk is responsible for developing a global validation standard for all new Fill Finish facilities sites, ensuring the quality of the final product during the manufacturing process. We develop and implement quality control plans and work closely with other departments to maintain quality standards. The department is staffed with highly qualified professionals and specialists who continuously develop and improve quality control processes from design to final validation.

 
Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 50,000 employees. Together, we go further. Together, we’re life changing.

Contact
For further information, please contact Lene Højgaard Christensen, Senior manager Quality Planning at +45 30796740.

Deadline
10 January 2025.

Please note, applications will be reviewed, and interviews will be conducted on an ongoing basis.

You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.