Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company is seeking an Associate Principal Scientist to optimize regulatory authoring processes. The role involves defining the roadmap for digitizing regulatory content, overseeing a cross-functional development team, and ensuring effective implementation of solutions. The ideal candidate will have significant experience in manufacturing processes and regulatory documentation. The position is based in Minnesota with a hybrid work model and involves collaboration with diverse teams to drive innovation and improve efficiency. #J-18808-Ljbffr