Global Regulatory CMC Lead — Hybrid, Strategy & Submissions

A leading biopharma company seeks a GRA CMC Lead in Framingham, MA to drive regulatory strategy for pharmaceutical products. The ideal candidate will have over 4 years of CMC regulatory experience, a scientific degree, and the ability to navigate complex regulatory requirements. Responsibilities include guiding products from development to market, collaborating with R&D, Manufacturing, and Quality teams, and ensuring high-quality regulatory submissions. This role offers competitive compensation and opportunities for professional growth. #J-18808-Ljbffr