Global Regulatory Affairs CMC Director — Submissions

A global biopharmaceutical leader based in Boston is seeking a GRA CMC Product Lead to develop and execute regulatory strategies for assigned products. The ideal candidate will have over 10 years of experience in the biopharmaceutical industry, with at least 8 years focused on regulatory CMC. Key responsibilities include leading submissions, mentoring team members, and representing the company in Health Authority meetings. This position offers a comprehensive compensation package, including competitive salary and benefits. #J-18808-Ljbffr