CAR-T Aseptic Manufacturing Associate – Liso-cel

Bristol-Myers Squibb Co; Summit (NJ); On-site; USD 79,744,000 - 96,622,000; Full time

Benefits offered by this job

Wellbeing support

Retirement benefits

Insurance (medical, dental, vision)

Job summary

Bristol Myers Squibb Co in Summit, NJ is seeking an Aseptic Manufacturing Associate for Liso-cel CAR-T manufacturing operations. You will support routine manufacturing in a cleanroom, ensure aseptic processing, and adhere to GMP and quality systems.

The role emphasizes safety, training, and documentation accuracy across multiple shifts. Onsite work with comprehensive benefits is provided.

Qualifications

• Proven teamwork experience in manufacturing or GMP environments.
• Proficiency with common office software (Word, Excel).
• Strong attention to detail and accountability.
• Excellent interpersonal and collaborative skills.
• Maintain professional relationships with management and coworkers.
• Basic understanding of cGMP regulations for biologics and cell therapy manufacturing is preferred.

Responsibilities

• Learn and execute Cell Therapy Manufacturing operations compliantly.
• Execute operations as outlined in Source Governing Documents (SOPs, Work Instructions, Batch Records, Forms).
• Perform transactions in electronic systems and adhere to business continuity processes.
• Prioritize safety of self and others.
• Report safety events within 24 hours.
• Escalate issues impacting compliance or safety.
• Complete documentation required by governing documents in real time.
• Maintain compliance with SOPs, quality systems and cGMP requirements.

Skills

Team collaboration

MS Office

Attention to detail

Interpersonal skills

Professional relationships

cGMP knowledge

Education

High school diploma

Associate or Bachelor's preferred

Job description

Bristol Myers Squibb Co in Summit, NJ is seeking an Aseptic Manufacturing Associate for Liso-cel CAR-T manufacturing operations. You will support routine manufacturing in a cleanroom, ensure aseptic processing, and adhere to GMP and quality systems.

The role emphasizes safety, training, and documentation accuracy across multiple shifts. Onsite work with comprehensive benefits is provided.