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- ...validation) to ensure GMP compliance Review and approve documents in both electronic systems (e.g. MES) and paper-based. Approve... ...manufacturing OR sterile drug substance manufacturing in a GMP controlled environment Experience in deviation and change management...EmpfohlenVollzeitTeilzeitarbeit
- ...batch execution. Responsible for new product introduction, process implementation, process control strategy and technical transfer and process validation documentation of assigned projects, including review of dossier modules for regulatory filing. Drive GMP...EmpfohlenVollzeit
- ...Process Development, Analytical Development, Regulatory Affairs, and Global MSAT to ensure seamless technology transfers, robust process control strategies, and successful commercialization of new products. Act as deputy to the Head of Drug Product Operations Stein as...EmpfohlenVollzeit