CMC Regulatory Affairs: Associate Director — Lead Submissions

AbbVie in the United States is seeking an Associate Director Regulatory Affairs, CMC to lead regulatory strategies and submissions for drug products. You will collaborate with internal teams and external partners, negotiating with agencies to enable first-pass approvals and driving strategic advisory within CMC on product development, regulatory submissions, and ongoing compliance. The role requires strong leadership, extensive experience in regulatory affairs, and the ability to navigate #J-18808-Ljbffr Allergan