Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical leader in Springfield, Illinois is seeking an Associate Principal Scientist to optimize regulatory authoring processes. This role involves defining roadmaps, directing project execution, and establishing data governance standards. Candidates should have a strong understanding of manufacturing and CMC operations, with experience in regulatory documentation and project management. This position offers a hybrid work model and requires strong communication skills and a collaborative approach. Join a diverse team focused on digital transformation in the pharmaceutical industry. #J-18808-Ljbffr