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

Role: Manufacturing Associate supporting the production of blood-derived cell therapy components within a cGMP cleanroom environment. Primary responsibilities include equipment setup and operation for cell culture, harvest, and cryopreservation processes; adherence to aseptic techniques; data recording; and supporting deviation investigations and CAPAs. Responsibilities extend to teamwork, training to SME level, process documentation, and participation in continuous improvement initiatives. Requirements: High School diploma (Bachelor's or Associate degree preferred); 0-1 year experience in cGMP cell therapy or bioprocess manufacturing; knowledge of cell culture, cryopreservation, aseptic processing, and regulated industry standards; basic math and technical writing skills; proficiency with MS Office; understanding of biology, chemistry, or clinical practices. HighValue: biologics (cell therapy, CAR-T), blood-derived components, manufacturing in a controlled GMP environment, supporting production shifts, and compliance with safety and quality protocols. WorkSetup: shift-based (Thurs-Sat, with alternating Wednesdays), in New Jersey; physically demanding environment requiring PPE compliance, working with human blood products, and potential exposure to sanitization agents. The role emphasizes teamwork, technical skill development, and operational excellence in cell therapy manufacturing.