MSAT Suite Coordinator, Cell Therapy in Devens, MA

Role: MSAT Suite Coordinator, Cell Therapy, supporting GMP manufacturing operations within Bristol Myers Squibb's cell therapy development. Objectives: oversee and coordinate equipment and systems critical to manufacturing continuity, audit readiness, and operational efficiency. Responsibilities: manage system administration, prioritize work with Facilities & Engineering, support vendor coordination, track work orders, maintain GMP compliance, assist in CAPAs, oversee spare parts and inventory, and drive process improvements. Collaborate with cross-functional teams including Manufacturing, Quality, Technical Services, and Engineering. Requirements: Bachelor’s or Associate degree and at least 3 years of experience in cGMP biotech/pharma manufacturing or related field; proficiency in Infinity, Syncade, DeltaV, SAP, Maximo preferred; strong organization, multitasking, and communication skills; Lean process knowledge (Yellow/Green Belt preferred). High-Value: cell therapy (likely CAR-T or other modalities), GMP manufacturing environment, equipment/system oversight, audit readiness, cross-functional collaboration. WorkSetup: on-site in Devens, MA with shift flexibility; specific travel not indicated.