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Director, Drug-Device CMC Regulatory Affairs

Merck, Jackson, MS, United States


A leading pharmaceutical company seeks a Director/Principal Scientist to oversee regulatory CMC activities for autoinjector and inhalation products. You will lead regulatory strategies, ensuring compliance and evaluating risks for product submissions. The ideal candidate will bring over 10 years of experience in pharmaceutical research and regulatory affairs, possess strong leadership and communication skills, and thrive in a dynamic hybrid work environment. A comprehensive benefits package is offered, alongside competitive compensation. #J-18808-Ljbffr