Global CMC Regulatory Consultant (Senior)

A global regulatory affairs firm is seeking a CMC Regulatory Affairs Senior/Consultant to join their team in the United States. The ideal candidate will have 4–6 years of CMC regulatory experience in the pharmaceutical industry, preparing regulatory documentation for FDA, EMA, and Health Canada. Responsibilities include providing regulatory strategy input, preparing CMC documents, and collaborating with cross-functional teams. This role demands strong analytical and communication skills, and candidates with advanced degrees are preferred. #J-18808-Ljbffr