Post-Approval CMC Strategy Director — Gene Therapy

A biopharmaceutical company in Somerville, Massachusetts is seeking a Senior Director, Regulatory CMC to lead regulatory strategy for gene therapy products. This hybrid role emphasizes lifecycle management and regulatory compliance. The ideal candidate will have at least 15 years of biopharmaceutical experience, particularly in post-approval regulatory affairs, with strong leadership and communication skills. Benefits include a competitive salary and comprehensive medical coverage, along with unlimited paid time off and parental leave. #J-18808-Ljbffr