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

Scorpion Therapeutics; Summit (NJ); On-site; USD 58,000 - 76,000; Full time

Job summary

Bristol Myers Squibb is seeking an Aseptic Manufacturing Associate for routine cell therapy production in New Jersey. The role focuses on Liso-cel CAR-T manufacturing, requiring adherence to GMP and aseptic processing standards in a controlled environment.

Onsite shifts in NJ, with responsibilities spanning documentation, SOP compliance, and participation in continuous process improvement and training activities.

Qualifications

• 0–1 year experience in cGMP bioprocessing, biologics, or cell therapy manufacturing.
• Basic understanding of GMP regulations and aseptic techniques.
• Proficiency with computer tools and data entry.
• Meticulous attention to detail and strong interpersonal skills.

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.

Skills

Attention to detail

Interpersonal skills

Proficiency with computer tools

Education

High school diploma

Associate or Bachelor’s preferred

Job description

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:

lifting, standing, PPE use, and working in controlled environments.