Academic for Validation and IT
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- Quality
- Bagsværd
Do you want to be a part of an experienced validation team? Would you like to work with validation of analytical methods for the future Diabetes and Obesity products? Do you want to join a dynamic department with the responsibility of technology to reduce lead time in direction towards real time release testing? Then you might be our new academic.
About the department
Analytical Competence Centre is a department in Diabetes Finished Products (DFP) Manufacturing Development and consists of 38 employees organised in 2 teams. We are responsible for valida-tion of analytical methods before clinical phase 3, and we secure implementation of the analytical methods at our production sites across the world.
Furthermore, the department is on a journey involving scouting, testing and implementing of new analytical techniques to reduce the lead time for analysis with the ambitious long-term goal of real time release testing of diabetes finished products. We strive to do all of this in a collabora-tive environment of joy and curiosity in our department.
The job
We are currently looking for a skilled academic for validation of analytical methods in a perma-nent position in the Validation and IT team, which consists of 6 academics and 11 laboratory technicians.
The team is responsible for maturing and validation of new analytical methods for Diabetes and Obesity products. This includes optimisation of analytical methods in close collaboration with CMC, validation and documentation in internal reports, and giving input to submission to documents for the authorities.
The analytical methods are primarily UPLC/HPLC - methods, but also includes AAS, pH, Freezing point depression and High Voltage Leak Detection. Going forward new analytical methods with the purpose of real time release testing will be introduced.
Our new academic will furthermore have an important role in the IT part of introducing new
analytical technics in DFP QC laboratories.
Your main stakeholders will be colleagues in the department, QA, CMC, Regulatory Affairs and QC laboratories. Traveling days might be expected.
Qualifications
You have a scientific academic degree such as cand. pharm., cand. scient., chemical engineer or similar. You have experience within validation of analytical methods and besides that, you have experience from a laboratory environment subject to GMP with one or several analytical tech-niques such as UPLC/HPLC, pH, AAS or container closure integrity. Interest in the IT part of quali-fication and optimisation of equipment, and handling of large amounts of data will be an advantage.
You are a team player, openminded, engaged and able to inspire and motivate your colleagues. We expect you to possess good communication skills in both oral and written English. You thrive in a changing environment with ambitious deadlines.
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 Palle Kristensen on +4530793025
Deadline
14 December 2020
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 30.11.2020, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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