Description
Editas Medicine is hiring a Senior QA Specialist to support advancement of EDIT-401 into the clinic by ensuring GMP, FDA, cGMP, and international regulatory compliance across manufacturing, testing, product disposition, and quality event management. The role is part of a small Quality team and involves batch record review, lot disposition, oversight of CDMOs/CTOs, authoring and approving GMP documentation, supporting quality systems and vendor management, and collaborating across early-phase biopharmaceutical operations.
