Associate Director, CMC Regulatory — CDMO Leader

A leading pharmaceutical company in Massachusetts is seeking an Associate Director, Regulatory CMC, to spearhead regulatory activities in a CDMO environment. The role requires extensive experience in CTD Module 3 authoring and DMF lifecycle management. Responsibilities include providing regulatory guidance to clients, managing communications with health authorities, and ensuring compliance with global regulations. The ideal candidate will possess strong project management and technical writing skills. The position offers a competitive salary ranging from $165,200 to $202,000 annually. #J-18808-Ljbffr