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

Role: Aseptic Manufacturing Associate supporting routine cell therapy production at Bristol Myers Squibb, focusing on Liso-cel CAR-T therapies. Responsibilities include executing manufacturing operations in compliance with GMP, SOPs, and batch records; maintaining environmental controls; performing aseptic processing within ISO cleanrooms; and ensuring documentation accuracy. The role involves operating in a BSL2 environment with human blood components, nitrogen exposure, and gowning protocols. Key tasks also encompass environmental monitoring, process refinement, and contributing to SOP development. Requirements: high school diploma (associate or bachelor’s preferred), 0-1 years' experience in cGMP bioprocessing, cell therapy manufacturing, or related fields; familiarity with GMP regulations and FDA guidance is preferred. Skills include attention to detail, teamwork, computer literacy, and safety adherence. The position demands physical ability to lift/push materials, work in PPE, and perform in controlled, sterile settings. The role operates on day shifts (Sunday-Wednesday or Wednesday-Saturday), onsite in NJ, with shift-specific physical and safety requirements. High-value biopharma specifics: focus on cell therapy (CAR-T), aseptic processing, cGMP compliance, human blood component handling, and environmental control within regulated biomanufacturing settings. The position emphasizes safety, GMP adherence, and process support to enable scalable cell therapy manufacturing.