Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Nashville, TN, seeks an Associate Principal Scientist to optimize regulatory authoring processes using innovative digital solutions. The role involves managing cross-functional teams and enhancing data governance principles. Candidates should have a background in chemistry or engineering, with experience in regulatory documentation and manufacturing processes. Join a collaborative environment focused on improving efficiencies in regulatory filings. This position offers a hybrid work model. #J-18808-Ljbffr