Global CMC Regulatory Consultant (Senior)

A global pharmaceutical consulting firm is looking for a CMC Regulatory Affairs Senior/Consultant in Dover, Delaware. The role requires 4–6 years of CMC regulatory experience, with a focus on preparing regulatory documentation and providing strategic guidance on small molecule and biologic products. The ideal candidate will thrive in a collaborative environment, possess strong analytical and communication skills, and have a solid educational background in Pharmaceutical Sciences. This position offers the chance to work in a dynamic regulatory landscape. #J-18808-Ljbffr