Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical company is seeking an Associate Principal Scientist to optimize regulatory authoring processes. This role involves working with cross-functional teams to implement digital solutions that enhance data management for regulatory submissions. The successful candidate will have considerable experience in regulatory authoring and strong skills in project management. Candidates should hold a B.S. or higher in chemistry or engineering and have substantial experience in the pharmaceutical industry. The position is hybrid with responsibilities in Frankfort, Kentucky. #J-18808-Ljbffr