Principal Manager, R&D GMP Pharmaceutical Sciences Quality EU & US (hybrid)
Takeda Pharmaceutical Company(2 months ago)
About this role
The Principal Manager, R&D GMP Pharmaceutical Sciences Quality EU & US provides quality oversight across investigational medicinal product development from early clinical stages through commercialization. The role supports diverse modalities (biologics, synthetic molecules, plasma-derived therapies, conjugates, combination products) and requires independent decision-making and cross-functional collaboration with CMOs and partners to ensure cGMP compliance and timely program progression.
Required Skills
- cGMP Compliance
- Quality Oversight
- Documentation Review
- Deviation Management
- CAPA
- Audits
- Supplier Qualification
- Stability Planning
- Cross-Functional Collaboration
- Technical Guidance
+2 more
Qualifications
- Bachelor's Degree in a Relevant Scientific Field
- Advanced Degree Preferred
About Takeda Pharmaceutical Company
takeda.comTakeda is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future.
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