Associate QA Director, Manufacturing QA

Employment type: Full time. Requisition: JR382. Start: 2026-09-16. Country: Denmark.

Does it excite you to work with GMP Quality Assurance for Drug Product and Combination Products in an outsourced development set-up, and do you have experience with QA oversight of CMOs, QP responsibilities, and cross-functional CMC collaboration? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new colleague.

Your new position As our Associate QA Director, you will provide QA oversight and compliant quality guidance for Drug Product and Combination Product development and GMP manufacturing performed at external CMOs and in close collaboration with partners. You will help ensure robust GMP execution and timely quality decisions.

In addition, the role contains delegated Qualified Person (QP) responsibilities for both clinical and commercial products, in accordance with applicable GMP legislation. The role also involves occasional travel to support effective oversight and collaboration with external sites. You will join Manufacturing QA in an outsourced business model where strong collaboration and clear quality judgment are key1 …