Senior CMC Regulatory Affairs Director

A leading biopharmaceutical company is seeking an Associate Director of Regulatory Affairs in Irvine, California. This role involves preparing regulatory strategies for Chemistry, Manufacturing, and Controls (CMC) and managing regulatory submissions. Candidates should have at least 8 years of pharmaceutical experience, with demonstrated leadership and expertise in global regulatory strategies. The successful applicant will work closely with regulatory agencies and internal teams to ensure compliance and efficient operations. Competitive compensation and comprehensive benefits are included. #J-18808-Ljbffr