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

Role: Manufacturing Associate in Cell Therapy production, focused on blood-derived component manufacturing under cGMP conditions. Responsibilities: operate equipment for cell culture, harvest, cryopreservation; support deviation investigations and CAPAs; maintain aseptic techniques; document production data; ensure compliance with safety, quality, and GMP standards; contribute to continuous improvement and training. Requirements: High school diploma; 0-1 years experience in cGMP cell therapy or bioprocessing manufacturing; basic understanding of cell culture, cryopreservation, and aseptic techniques; knowledge of industry regulations; proficiency with MS Office; capable of working in cleanroom environments and handling human blood components. Preferred: Bachelor's or associate degree, technical writing skills. High-Value: Focus on cell therapy (likely CAR-T), blood components, cGMP regulated, manufacturing stage in clinical or commercial production, maintaining compliance with FDA regulations, working in a cleanroom setting, on-site shift with physical requirements, and team-based environment.