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

Role: Manufacturing Associate in Cell Therapy, focused on producing blood-derived components for CAR-T therapy (liso-cel) in a cGMP cleanroom environment. Responsibilities: operate equipment for cell culture, harvest, cryopreservation; support deviation investigations and CAPA closures; perform aseptic techniques; record data per GDP; work within production schedules; participate in continuous improvement and inspection readiness initiatives. Requirements: High School diploma; 0-1 years experience in cGMP cell therapy or bioprocessing; basic understanding of cell culture, cryopreservation, aseptic processing, and GMP regulations; proficiency in MS Office; technical writing skills. Preferred: Bachelor's or associate degree. High-value specifics: manufacturing of human blood components for CAR-T cell therapy, working in a regulated, controlled environment with exposure to human blood, chemicals, and sanitization agents. Collaboration: team-based, cross-functional environment supervised by shift management. Work setup: onsite day shift in Summit West, NJ, with specific shift hours; physical dexterity required; ability to work in restricted cleanroom areas with PPE; physical ability to lift 25 pounds. The role emphasizes compliance with safety, quality, and GMP standards, contributing to innovative biopharma manufacturing of advanced cell therapies.