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Manufacturing Team Lead, Liso-cel CAR-T, Manufacturing Operations

Job in Summit, Union County, New Jersey, 07902, USA
Listing for: Bristol Myers Squibb
Full Time position
Listed on 2025-12-01
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production Manager, Operations Engineer
Job Description & How to Apply Below

Manufacturing Team Lead, Liso‑cel CAR‑T, Manufacturing Operations

2 days ago Be among the first 25 applicants

Working with Us:
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. Read more at

At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best‑in‑the‑industry team and long‑term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.

As a Manufacturing Team Lead, you will manufacture human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable.

Shift

Available
  • Sunday - Wednesday (with e/o Wednesday off), Onsite Night Shift, 5 p.m.

    - 5 30 a.m.
Responsibilities
  • Oversee set‑up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
  • Lead deviation investigations and write‑ups as needed.
  • Accountable for on-time closure of any assigned CAPAs within the designated shift.
  • Aseptic technique is required for tube most activities welding, connections, and transfers, at minimum.
  • Aseptic qualification is required.
  • Weighs and measures in-process materials to ensure proper quantities are added/removed.
  • Adheres to the production schedule ensuring on-time internal production logistics.
  • Records production data and information in a clear, concise format according to proper GDPs.
  • Perform all tasks in a manner consistent with site safety policies, quality systems, and GMP requirements.
  • Works in a team based, cross‑functional environment to complete production tasks required by shift schedule.
  • Motivated, team consciousness individuals are needed to fulfill job requirements.
  • Is a SME and qualified trainer within a designated function of manufacturing.
  • Team Lead is responsible for the designated area within the shift.
  • Shift supervision will be managed by the shift Supervisor, but Team Lead will act as Supervisor when needed.
  • Maintain on-time completion of training assignments and those of the associates in the designated area to ensure the necessary technical skills and process knowledge required to execute operations in a GMP compliant manner.
Knowledge & Skills
  • Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique.
  • Knowledge of cGMP/FDA regulated industry.
  • Basic mathematical skills.
  • General understanding of cGMPs.
  • Technical writing capability.
  • Proficient in MS Office applications.
  • Background to include an understanding of biology, chemistry, medical or clinical practices.
  • Pre‑requisites Senior Associate in Manufacturing.
Basic Requirements
  • Bachelor’s degree and 4 years of experience in cell therapy in Biopharmaceutical operations.
  • Or Associate / Medical Technical degree and 6+ years of Manufacturing Operations experience.
  • Or High School diploma/GED…
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