Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical company is seeking an Associate Principal Scientist to enhance data management and optimize regulatory authoring processes. This role involves defining and maintaining a roadmap for digital CMC initiatives and working with cross-functional teams to develop solutions. Key requirements include strong knowledge of manufacturing processes and hands-on experience in regulatory authoring. This position offers a competitive salary and opportunities for growth in a hybrid work environment. #J-18808-Ljbffr