AbbVie in Massachusetts seeks an Associate Director Regulatory Affairs (CMC) to lead strategy and submissions for regulatory approvals and changes. You will collaborate with Product Development, R&D and Operations to guide global CMC programs and liaise with health authorities.
The role requires extensive regulatory experience, leadership, and strong communication skills to navigate complex environments and drive first-pass approvals.
#J-18808-LjbffrAssociate Director, CMC Regulatory Strategy & Submissions in waltham at Unknown Company
This position is listed as full time and onsite.