CGT CMC Regulatory Affairs Lead

A leading biopharmaceutical company seeks an Associate Director in Regulatory Affairs to lead the CMC strategy for their Cell & Gene Therapies pipeline. Responsibilities include managing regulatory submissions, ensuring compliance with global regulations, and collaborating with cross-functional teams. Ideal candidates will have a strong background in gene therapy with at least 10 years of experience in regulatory roles. This hybrid role offers a competitive salary package and benefits. #J-18808-Ljbffr