CMC Regulatory Affairs Lead – Submissions & Strategy

A leading global biopharmaceutical company is seeking an Associate Director in Regulatory Affairs, focused on Chemistry, Manufacturing, and Controls (CMC). This role prepares and manages regulatory submissions, develops strategies for product applications, and leads cross-functional teams. Candidates should have a degree in a relevant field and significant experience in the pharmaceutical industry, especially in regulatory affairs. Strong leadership and communication skills are essential. This position offers a competitive compensation package and various benefits. #J-18808-Ljbffr