Analytical Chemist
Novo Nordisk
Would you like to work on the validation of analytical methods for the future Diabetes and Obe-sity products? Do you want to be involved in validating of analytical methods of the future? Are you interested in joining a dynamic department responsible for validation, site support and im-plementation of new technology?If so, you could be our new Analytical Chemist based in Bagsværd. Read on to find out more and apply today and join us for a life changing career!The position
We are seeking an experienced Analytical Chemist to join us on a permanent basis. As the new Analytical Chemist, you will join the Validation team and will be ensuring the optimisation, vali-dation, and implementation of analytical methods. The team’s focus is on refining and validating new analytical methods for Diabetes and Obesity products. This involves optimizing of analytical methods in close collaboration with CMC (Chemistry, Manufacturing and Control), validation, and documentation in internal reports, and giving input to submission to documents for the au-thorities.You will play a leading role in:
Furthermore, new analytical methods with the purpose of real time release testing will be intro-duced, and our new analytical chemists will have a role in validation and implementation of these technologies.Main stakeholders will include colleagues in the department, Quality Assurance (QA), Regulatory Affairs, and our Quality Control (QC) laboratories.QualificationsTo succeed in this role you have:
As a Chemist, you thrive in a dynamic environment and collaborate with colleagues to meet am-bitious deadlines. Additionally, you are a team player, open-minded and possess excellent communication skills to inspire and motivate colleagues.About the department
Analytical Competence Centre is a department in Injectable Finished Products (IFP) Manufactur-ing Development and consists of around 65 employees organised into 5 teams. We are the cen-tral function for analysis of Novo Nordisk Injectable Finish Products during late-stage develop-ment, as well as for marketed products. The department is responsible for validation of analyti-cal methods before process validation in the production, and for the subsequent transfer and ownership of those methods to our QC laboratories across the world.
Additionally, the department is involved in testing, validation and implementing of new analyti-cal techniques to reduce the lead time for analysis, with the ambitious long-term goal of real time release testing of diabetes and obesity finished products.
Bagsværd, Hovedstaden
Wed, 22 May 2024 22:58:14 GMT
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