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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
Currently we are seeking a highly motivated and team-oriented candidate to create, communicate and execute DMPK strategy as a project representative person within integrated discovery project teams, facilitating the identification and development of drug
Define and lead the execution of global regulatory CMC strategies for device & combination products to ensure successful approvals in key markets and Compliance throughout development and lifecycle. Performs risk analysis for determination of probability
You lead the site Quality organization and serve as the key authority for GMP compliance and quality strategy. In this executive leadership role, you shape the site’s quality culture while enabling the successful delivery of innovative therapies,