
Director, Drug-Device CMC Regulatory Affairs
Merck, Trenton, NJ, United States
A leading global biopharmaceutical company is seeking a Director/Principal Scientist to oversee regulatory CMC activities for various drug delivery systems, including autoinjectors and inhalation products. The ideal candidate will have at least 10 years of experience in biological or pharmaceutical research, strong leadership and communication skills, and a proven track record in regulatory affairs. This role offers a hybrid work environment and a comprehensive benefits package.
#J-18808-Ljbffr