
Director, Drug–Device CMC Reg Affairs (Autoinjector)
Merck, Cheyenne, WY, United States
A leading healthcare company is seeking a Director/Principal Scientist for Devices and Drug-Device Combinations Regulatory CMC. This role involves leading regulatory strategies for autoinjector and inhalation products, ensuring compliance with global regulations. The ideal candidate should have at least 10 years of experience in biological research, regulatory affairs, and a strong background in technical writing and leadership. A hybrid work model is available.
#J-18808-Ljbffr