Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company is seeking an Associate Principal Scientist to optimize regulatory authoring and enhance data management. This role involves working with cross-functional teams to develop solutions that digitize regulatory documentation processes. Applicants should have a strong background in manufacturing and supply chain processes relevant to regulatory filings. The position requires excellent project management and communication skills, with a focus on driving accountability and achieving results. #J-18808-Ljbffr