Associate Director, QA GMP

About the role

Genmab is seeking an experienced QA Associate Director for Chemical Intermediates (CI), Biological Intermediates (BI), and Drug Substance (DS) to direct Quality Assurance oversight of CI, BI, and DS activities supporting commercial products, all manufactured through external partners. In addition, the role contains Qualified Person (QP) responsibilities for CI, BI, and DS activities supporting commercial products as reported in the company Manufacturing and Import Authorization (MIA). This role plays a critical part in safeguarding product quality, patient safety, and supply reliability in a fully outsourced manufacturing model. You will be an important part of the global GMP QA organization to ensure compliance with industry standards and regulations in relation to commercial CI, BI, and DS manufacturing. The position will be located in Denmark reporting to the Director of GMP QA Commercial, Drug Substance & Intermediate.

Responsibilities