Manufacturing Associate - Summit West, NJ

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

Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Biopharmaceutical Manufacturing | Day Shift (Quad
1) | cGMP Cleanroom Environment

About the Role

The Manufacturing Associate is responsible for producing human blood-derived components in a controlled, cGMP cleanroom environment in accordance with Standard Operating Procedures (SOPs) and regulatory requirements. This role operates within a collaborative, shift-based team structure and plays a critical part in ensuring the quality, safety, and timely delivery of life-changing therapies.

Shift

Schedule:

Quad 1 — Sunday through Wednesday, 5:00 AM – 5:30 PM Start and end times are subject to change based on business needs.

This position reports directly to the Manufacturing Manager, with day-to-day supervision provided by the shift Supervisor or designated Team Lead.

• Production & Operations
• Set up and operate equipment to support blood component production through cell culture, harvest, and cryopreservation
• Apply aseptic technique for all applicable activities, including tube welding, connections, and transfers; aseptic qualification is required
• Weigh and measure in-process materials to ensure accurate quantities are added or removed
• Adhere to the production schedule to support on-time, internal production logistics
• Quality & Compliance
• Record production data clearly and concisely in accordance with Good Documentation Practices (GDPs)
• Support deviation investigations and write-ups as needed
• Ensure on-time closure of assigned CAPAs within the designated shift
• Perform all tasks in alignment with site safety policies, quality systems, and GMP requirements
• Team & Development
• Work in a team-based, cross-functional environment to fulfill shift production requirements
• Develop subject matter expertise (SME) and become a qualified trainer within a designated manufacturing function
• Maintain timely completion of all training assignments to uphold technical skills and process knowledge
• Contribute to continuous improvement projects, inspection readiness, and right-first-time initiatives, as assigned

Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or laboratory technique

Familiarity with cGMP and FDA-regulated industry standards

Strong technical writing capability

Basic mathematical skills with a general understanding of cGMPs

Proficiency in Microsoft Office applications

Background in biology, chemistry, or medical/clinical practices preferred

Prior experience in manufacturing and/or a scientific or engineering discipline