Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical company is seeking an Associate Principal Scientist to drive digital solutions in Regulatory Authoring. This role involves optimizing workflows, establishing data governance standards, and working closely with cross-functional teams. The ideal candidate has extensive experience in regulatory documentation and project management, along with a strong knowledge of CMC operations. Successful candidates will work in a hybrid model and assist in streamlining regulatory processes to enhance efficiency across the organization. #J-18808-Ljbffr