Global Regulatory Affairs CMC Lead: Submissions & Strategy

A leading biopharmaceutical company in Boston, MA is seeking a dedicated individual for the role in Global Regulatory Affairs focused on Chemistry Manufacturing & Controls. The ideal candidate will have over 10 years of experience in the biopharmaceutical/device industry, with a strong background in regulatory CMC. Responsibilities include managing regulatory submissions and liaising with Health Authorities. This role offers hybrid work options and a competitive salary range, ensuring equitable pay for all employees. #J-18808-Ljbffr