Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company is seeking an Associate Principal Scientist to drive digital transformation initiatives in regulatory authoring. The candidate will work collaboratively with cross-functional teams to optimize processes and ensure data governance. The ideal candidate has extensive experience in the pharmaceutical industry, strong project management skills, and knowledge of regulatory requirements. This role is based in Lansing, Michigan, and offers a hybrid work model. #J-18808-Ljbffr