Principal Manager, R&D GMP Pharmaceutical Sciences Quality EU - Zurich, Zurich
vor 21 Stunden

Job summary
The Principal Manager, R&D GMP Pharmaceutical Sciences Quality EU & US provides Quality oversight across Takeda's investigational medicinal product development lifecycle, from early clinical development through commercialization.Responsibilities
- Oversee final release and disposition of Clinical Trial Material across multiple modalities and complex development programs.
- Review and approve batch documentation, master/executed records, labels, specifications, analytical methods, protocols, and stability plans.
Stellenbeschreibung
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