Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations

Role: Manufacturing Associate in Cell Therapy manufacturing, supporting blood-derived component production in a cGMP cleanroom. Responsibilities: operate equipment for cell culture, harvest, cryopreservation; support deviation investigations and CAPA closures; perform aseptic techniques; record data per GMP standards; collaborate within a team and contribute to continuous improvement initiatives. Requirements: high school diploma or equivalent; 0-1 year experience in cGMP cell therapy or bioprocessing; basic understanding of cell culture, cryopreservation, and aseptic processing; knowledge of GMP/FDA regulations; proficiency in MS Office; technical writing skills. Preferred: associate or bachelor's in related fields. High-Value: biologics, cell therapy, blood-derived products, manufacturing stage focused on process support, regulatory compliance, and aseptic environment. Work setup: onsite overnight shift (Wed-Sat, 5 p.m. - 5:30 a.m.); physical ability to work in controlled, restricted environments; PPE required; potential exposure to human blood components. This role emphasizes compliance, teamwork, technical skill development, and supporting manufacturing of innovative cell therapies.