Associate Director, CMC Regulatory Affairs - Heme/Oncology

Regeneron Pharmaceuticals is seeking an Associate Director based in Dublin, Ireland to lead CMC regulatory strategies for hematology and oncology portfolios. In this role, you will mentor staff, manage product development activities, and serve as a liaison with regulatory authorities.

The ideal candidate has over 10 years of experience in the pharmaceutical/biotech industry and a strong understanding of CMC regulations. The position requires in-office work 3 days a week and offers a range of competitive benefits.