Associate Director, QA GMP

About the role

Genmab is seeking an experienced GMP QA Associate Director for Chemical Intermediates (CI), Biological Intermediates (BI), and Drug Substance (DS) to provide strategic and operational Quality Assurance oversight of development-stage manufacturing activities supporting clinical trials, all conducted through external manufacturing partners. This role is key to ensuring product quality, patient safety, and reliable supply within a fully outsourced development manufacturing network. Working closely with CMOs and cross-functional stakeholders, you will contribute to maintaining a strong quality culture and ensuring compliance with applicable GMP requirements throughout the development lifecycle. You will become part of Genmab's global GMP QA organization and play an important role in supporting development programs and outsourced manufacturing activities for CI, BI, and DS products. The position is based in Denmark and reports to the Director of GMP QA Development, Drug Substance & Intermediates.