The CAR-T Manufacturing Supervisor is responsible for directing the daily production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Their job duties will be performed within a team-based environment, on an assigned production shift schedule. This role involves leading and supervising a specific Processing Manufacturing Unit within the CART process operations (Day 0, Cell Culture, Day 10 or Component Prep). The supervisor will lead daily shift operations meetings, assign production tasks, ensure compliance, and provide clear guidance to operations personnel. They will also support manufacturing investigations, create/revise operational procedures, and handle change controls. Collaboration with the Operations Manager for personnel development and performance input is key. Building positive relationships with Manufacturing, Engineering, and Quality is essential for seamless execution and issue resolution. The role also supports the development of manufacturing processes, drives continuous improvements, and participates in department projects and critical production runs when needed. Supervisors are expected to stay with their processing unit until batches are completed, even if it extends beyond the shift end time.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree