Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Baton Rouge is seeking an Associate Principal Scientist to optimize regulatory authoring processes within a digital initiative. This role entails defining roadmaps, directing cross-functional teams, and ensuring compliance with regulatory standards. Candidates should possess extensive experience in pharmaceutical regulations, effective project management skills, and a commitment to data governance. The successful applicant will drive digital transformation and enhance operational efficiency within the company. #J-18808-Ljbffr