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The role will provide scientific and technical leadership for analytical development at various stages of drug development both internal and external through CDMO with particular emphasis on research and early development (pre-DP0) including material
This role is accountable for defining the vision, operating model, and multi-year strategy for internal QC to support Genmab’s evolving pipeline and transition to a fully integrated, commercial-stage biotechnology company. The role will shape future QC
You will be a contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance system, adverse drug experience (ADE) reports, trending reports, ADE
Lead and execute the country/regional Medical Affairs strategy, representing the medical function internally and externally, including interactions with health authorities and cross‑functional teams. Build and maintain strategic scientific partnerships
Ensure commercial Drug Product batches are manufactured and released in time to guarantee continuous supply to all global markets. Ensure a timely arrival of Drug Substance shipments and allocate Drug Substance to the Drug Product batches, taking into