Associate Manager, CMC Regulatory Affairs
About this role
Associate Manager, CMC Regulatory Affairs
Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, CMC Regulatory Affairs to join our Regulatory Affairs team, supporting our Japan organization in a hybrid work mode. In this role, you will support regulatory CMC strategy and submissions across therapeutic areas while collaborating with Global Regulatory CMC, CMC Regulatory Science, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where:
Location: Tokyo, Japan
Working model: Hybrid
Discover your role:
- Support planning, scientific writing, and critical review of CTN, J-NDA, and eCTD supplement submissions.
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