The Steely Group is seeking a CMC QA Consultant to support cross-functional teams across PD, MSAT, CMC, Manufacturing and Regulatory Affairs to ensure quality and compliant controls for gene therapy programs.
You will review batch records, deviations, tech transfers, and regulatory submissions, lead QA oversight of process validation and CMO/QMS activities, and ensure compliance with cGMP throughout development to commercialization.
#J-18808-LjbffrCMC QA Associate: Gene Therapy & cGMP Expert in bedford at Unknown Company
This position is listed as full time and onsite.