Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company is seeking an Associate Principal Scientist in Little Rock, Arkansas. This role involves optimizing regulatory authoring processes and enhancing data management within a digitized framework. The ideal candidate will have extensive knowledge in manufacturing and CMC operations, with experience in regulatory authoring and data governance. Strong project management and communication skills are essential, contributing to a streamlined approach to regulatory filings. #J-18808-Ljbffr