Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations (in Summit, NJ)

Bristol Myers Squibb; West Summit (UT); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Manufacturing Associate to join their innovative team in Summit, NJ. This role offers a unique opportunity to work in a cutting-edge cleanroom environment, contributing to life-changing cell therapy advancements. You will be involved in the production of human blood-derived components, ensuring adherence to strict regulatory standards while collaborating with a dedicated team. If you are passionate about making a difference in patient lives and thrive in a dynamic work environment, this position is perfect for you.

Benefits

Flexible Work Arrangements

Comprehensive Benefits

Diversity and Inclusion Programs

Qualifications

• Experience in manufacturing or relevant scientific/engineering education.
• High school diploma/GED with 2+ years manufacturing experience.

Responsibilities

• Operate equipment for blood component production via cell culture and cryopreservation.
• Assist with deviation investigations and ensure quality compliance.

Skills

Cell Culture

Cryopreservation

Aseptic Processing

Technical Writing

MS Office Proficiency

Education

High School Diploma/GED

Technical Degree

Bachelor's Degree

Job description

Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations (in Summit, NJ)

Join Bristol Myers Squibb as a Manufacturing Associate, Liso-cel CAR-T, Manufacturing Operations in Summit, NJ. Be among the first 25 applicants to apply for this exciting opportunity.

We offer a challenging, meaningful, and life-changing work environment where every day brings new opportunities to contribute to groundbreaking cell therapy advancements that transform patient lives. Our culture promotes growth, innovation, and collaboration across departments.

The role involves manufacturing human blood-derived components in a controlled, cGMP cleanroom environment under supervision, adhering to regulatory standards, and working within a team on a rotating shift schedule. Responsibilities include supporting production processes, equipment setup, deviation investigations, aseptic techniques, data recording, and contributing to continuous improvement initiatives.

Shifts available: Wednesday to Saturday or Sunday to Wednesday, 12-hour shifts (5 p.m. to 5:30 a.m. or 5 a.m. to 5:30 p.m.).

Key Responsibilities:

• Operate equipment supporting blood component production via cell culture, harvest, and cryopreservation.
• Assist with deviation investigations and CAPA closures.
• Maintain aseptic techniques and proper documentation.
• Support production schedules and ensure quality and safety compliance.

Knowledge & Skills:

• Understanding of cell culture, cryopreservation, and aseptic processing.
• Knowledge of cGMP/FDA regulations.
• Technical writing and proficiency in MS Office.

Minimum Requirements:

• Experience in manufacturing or relevant scientific/engineering education.

Preferred Qualifications:

• High school diploma/GED with 2+ years manufacturing experience, OR technical degree with 3+ years, OR bachelor's degree.

Working Conditions:

• Ability to work in a cleanroom environment, lift 25 pounds, and work around biological materials.

At Bristol Myers Squibb, we value diversity and inclusion and offer flexible work arrangements and comprehensive benefits. We are committed to reimagining cell therapy and making a difference in patients' lives. If you're ready to challenge yourself and grow your career, apply today.