Biologics CMC Regulatory Affairs Lead
Listed on 2026-10-20
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Pharmaceutical
Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Pharmaceutical Science/ Research -
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Regeneron Pharmaceuticals Inc. seeks a Manager, CMC Regulatory Affairs - Biologics to lead regulatory strategy across development, submissions, and post‑market programs for its biologics portfolio.
This on‑site role collaborates with Global Regulatory Affairs and CMC teams to ensure compliance and timely filings. The position requires 6+ years in pharma/biotech or 3+ years with an advanced degree, with experience delivering CMC sections of MAAs, CTAs/INDs, and post‑approval submissions.
Consider building your career as a Biologics CMC Regulatory Affairs Lead at Regeneron Pharmaceuticals Inc.
We are looking to fill the Biologics CMC Regulatory Affairs Lead position at Regeneron Pharmaceuticals Inc. in Warren Township, NJ, United States.
The Biologics CMC Regulatory Affairs Lead role at Regeneron Pharmaceuticals Inc. is now open for applications in Warren Township, NJ, United States.
Join us at Regeneron Pharmaceuticals Inc. as our next Biologics CMC Regulatory Affairs Lead in Warren Township, NJ, United States.
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