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Director, Drug-Device CMC Regulatory Affairs

Merck, Augusta, ME, United States


A global biopharmaceutical company is seeking a Director/Principal Scientist for regulatory CMC activities. The role involves leading Device Regulatory Affairs strategies and ensuring compliance across various pharmaceutical products. Candidates should possess a robust background in biological sciences along with strong leadership skills and effectively communicate complex regulatory issues. The role is based in Augusta, Maine, and offers a hybrid work model with competitive salary and benefits. #J-18808-Ljbffr