Sr Reference Material Professional

Senior Reference Material Professional (Level 7) REQ 343770 Location:

Måløv, Denmark Job Category:

Research & Early Development Are you an experienced pharmaceutical scientist who enjoys working in a combined setup with both coordination activities and preparation of detailed documentation that directly support the development of life-changing medicines?

Would you like to play a pivotal role in ensuring analytical reference materials are available throughout the entire pharmaceutical development lifecycle from early clinical development through to commercial manufacturing? Do you thrive in a collaborative environment where scientific expertise, regulatory documentation, stakeholder management and continuous improvement are equally important?

If so, you could be our new Senior Reference Material Professional within Analytical Development at Novo Nordisk. About the Department You will join the Reference Materials team within Analytical Development, part of Analytical Characterisation in Chemistry, Manufacturing & Control (CMC).

The team is responsible for establishing reference materials for analysis of drug substance and drug product to support the entire development portfolio at Novo Nordisk. Our work spans from early Phase I development through Phase II, Phase III, and regulatory submissions. Although part of Analytical Development, this is not a laboratory-based role1 …