Analytical Life Cycle Management (LCM) Senior Specialist

About the role

At Genmab, we're committed to transforming the lives of people with cancer through innovative antibody therapeutics. As part of our continued growth, we are looking for a Life Cycle Management (LCM) Senior Specialist in the CMC Analytical & Characterization Department within CMC MSAT in CMC Development & Manufacturing / Technical Operations . In this role, you will contribute to our antibody-based modalities LCM projects, including e.g. Bispecific Antibodies and Antibody-Drug Conjugates (ADCs) . You will join a highly specialized CMC Analytical and Protein Characterization department, working as a Subject Matter Expert in an international, collaborative, and matrix environment. You will partner closely with: CMC LCM Project Managers. CMC MSAT colleagues across CMC Process Development, CMC Stability, CMC Pharmaceutical Development, and CMC Writing. Cross-functional stakeholders in Quality (QA), Regulatory CMC, Product Development (our non-GMP CMC development lab in Utrecht, NL), and Genmab QC (Ballerup, DK). External partners, including Contract Manufacturing Organizations (CMOs) in a network across the globe. Your work will be central to ensuring robust analytical overview , enabling successful support to regulatory submissions (BLA/MAA), post approval activities, and lifecycle management, and to ensure smooth transition from development to commercial LCM. At Genmab, collaboration, scientific excellence, and accountability are at the heart of everything we do - and your contributions will directly support our mission to bring impactful therapies to patients.