AbbVie in Irvine, CA is seeking an Associate Director Regulatory Affairs, CMC to develop and execute regulatory strategies for CMC submissions (INDs/CTAs, amendments) and to collaborate with R&D and Operations. You will lead cross-functional teams, prepare agency submissions, manage change controls, and communicate with regulatory authorities to support first-pass approvals.
Ideal candidate has 8+ years pharma experience with leadership in regulatory affairs and a strong track record in global
#J-18808-LjbffrCMC Regulatory Affairs Lead – Associate Director in irvine at Unknown Company
This position is listed as full time and onsite.