Associate Manager CMC Regulatory Affairs
Regeneron Pharmaceuticals(11 days ago)
About this role
The Associate Manager – CMC Regulatory Submissions Compliance supports the review and coordination of clinical trial application submissions within CMC Regulatory Affairs. The role involves ensuring documentation meets global requirements and maintains compliance in biopharmaceutical manufacturing.
Required Skills
- Regulatory Submissions
- CMC
- Biopharmaceuticals
- Documentation Coordination
- Quality Principles
- Regulatory Compliance
- Cross-functional Collaboration
- Program Management
- Clinical Trials
- Communication
Qualifications
- BS/BA in Chemistry or Biology
- 5+ years experience in biopharmaceutical manufacturing or related industry
About Regeneron Pharmaceuticals
regeneron.comDiscover how Regeneron (NASDAQ: REGN) harmonizes biology and technology to create life-changing medicines. Join our team and explore clinical trials.
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