Quality
Senior Manager, QA Commercial Drug Substance & Intermediates
Summary
Provides GMP quality oversight for commercial Drug Substance and Biological Intermediates manufactured by external CMOs. The role covers quality systems, supplier oversight, batch review and release, and resolution of quality issues.
Read by AI
Opportunity summary
Employment type: FULLTIME. Requisition: R17908. Hours: 40 hours per week. At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases.
We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science.
We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us!
The Role & Department The role is a senior quality specialist responsible for GMP quality oversight of commercial Drug Substance (DS) and Biological Intermediates (BI) manufactured at external Contract Manufacturing Organizations (CMOs). The role is based in Denmark and reports to the Director of QA Commercial – Drug Substance & Intermediates1 …
This is a shortened extract from the public vacancy. Follow the original posting for the complete and authoritative description.