Director, Drug-Device CMC Regulatory Affairs

A global healthcare leader is seeking a Director/Principal Scientist in Denver, CO, to lead Device Regulatory Affairs for innovative delivery systems. Candidates must have 10 years of experience in regulatory CMC, especially for autoinjectors and inhalation products, with strong technical writing and communication skills. This role emphasizes compliance, collaboration with cross-functional teams, and continuous learning. The position offers a hybrid work model and competitive compensation, reflecting expertise and experience. #J-18808-Ljbffr