Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical company is seeking an experienced Associate Principal Scientist to optimize regulatory authoring processes in Raleigh, North Carolina. This role involves managing a roadmap, leading cross-functional teams, and ensuring data governance for regulatory filing. The ideal candidate holds a degree in chemistry or engineering, with extensive experience in the pharmaceutical industry. This opportunity offers a hybrid work model with competitive compensation. #J-18808-Ljbffr