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 manufacturing. Responsibilities: execute GMP-compliant manufacturing operations in a cleanroom environment; follow SOPs, work instructions, and batch records; perform aseptic processing, environmental monitoring, and equipment handling; ensure safety, quality, and regulatory compliance; document operations accurately; participate in process refinement and training. Requirements: high school diploma (Associate or Bachelor’s preferred); 0-1 years experience in cGMP bioprocessing, biologics, or cell therapy manufacturing; basic understanding of GMP regulations and aseptic techniques; proficiency with computer tools; meticulous attention to detail; strong interpersonal skills. High-Value: cell therapy, CAR-T, GMP, aseptic processing, cleanroom environment, BSL2, handling human blood components, working in ISO 5 biosafety cabinets, and shift work (day shift available). Work setup: onsite in NJ, with specified shifts. Additional physical requirements include lifting, standing, PPE use, and working in controlled environments.