CMC Dossier Leader: Regulatory Submissions & Biologics

A leading biopharma company is seeking a CMC Dossier Leader in Framingham/Waltham, MA. This role involves leading the CMC dossier preparation for regulatory submissions, ensuring alignment with core CMC activities, and contributing to cross-functional project success. Candidates should have over 5 years in CMC development with a proven track record in dossier authorship, alongside strong leadership skills and a deep understanding of the pharmaceutical landscape. The company offers a comprehensive benefits package along with opportunities for career growth. #J-18808-Ljbffr