Director, Global Regulatory Affairs CMC
Takeda Pharmaceutical Company(16 days ago)
About this role
This role within Takeda's Global Regulatory Affairs Chemistry Manufacturing and Controls team involves developing and executing regulatory strategies for drug products, ensuring compliance, and supporting global submissions throughout the product lifecycle. The position offers an opportunity to lead complex regulatory projects in a dynamic, innovative environment focused on transformative therapies.
Required Skills
- Regulatory Strategy
- CMC
- Global Submissions
- Regulatory Affairs
- Drug Development
- Health Authority Interaction
- Project Leadership
- Regulatory Compliance
- Technical Documentation
- Team Leadership
Qualifications
- BS/BA in Scientific Discipline
- 10+ years pharmaceutical Regulatory CMC experience
- Advanced Degree (M.S., Ph.D.)
- Experience in biopharmaceuticals or devices
- Proven leadership in regulatory submissions
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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