CMC Dossier Lead: Regulatory Submissions & Strategy

A biopharmaceutical company in Framingham, Massachusetts, is seeking a CMC Lead to manage dossier preparation and ensure regulatory submission compliance. Candidates should have over 5 years of experience in CMC development and a proven track record in authoring dossiers. The role emphasizes collaboration and leadership within cross-functional teams, making it essential for candidates to possess strong communication skills and a deep understanding of the pharmaceutical landscape, including regulatory challenges and digital innovation. #J-18808-Ljbffr