Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Boston is seeking an Associate Principal Scientist to optimize regulatory authoring processes and enhance data management. The ideal candidate will work closely with cross-functional teams to implement digital solutions that improve regulatory filing workflows. Candidates should have a background in manufacturing, substantial regulatory authoring experience, and a degree in a related field. This position offers a hybrid work model. #J-18808-Ljbffr