CMC Regulatory Affairs Lead – Cell & Gene Therapy

A biotechnology company located in Cambridge, MA seeks an Associate Director of Regulatory Affairs - CMC to lead regulatory strategy for cell and gene therapy products. Responsibilities include interfacing with health authorities, preparing regulatory submissions, and managing complex projects. Candidates must possess a Bachelor's degree in Regulatory Science with 6 years of experience in Regulatory Affairs. The role allows telecommuting with some travel required within the US and Canada. #J-18808-Ljbffr