Supports implementation, configuration, and maintenance of the Manufacturing Execution System (MES) and electronic batch records for GxP-compliant cell and gene therapy manufacturing, including validation (UAT, IQ/OQ/PQ) and day-to-day user support. Requires pharma MES experience (e.g., POMSnet, Syncade, PAS-X) and SQL/scripting, on-site in Hopkinton, MA.
Sign in to see your match