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Associate Director, Team Lead, QA GMP @ Genmab

Copenhagen, Capital, DenmarkOnsiteFull-timePosted 19 days ago

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About this role

Embrace the opportunity to become an Associate Director, Quality Assurance (GMP) and lead a high-performing team in ensuring GMP compliance for drug product and clinical supply manufacturing. Drive quality improvements, manage audits, and collaborate with global stakeholders to advance innovative therapies in a dynamic, international environment. Shape the future of cancer treatment with Genmab.. Category: Development

Skills

gmp compliancequality assuranceaseptic drug product manufacturingclinical supply managementcapa managementchange controlrisk assessmentinternal auditregulatory inspectionstakeholder managementsupplier managementquality agreementsclinical trial supply oversightdeviation managementbatch release

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