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Manufacturing Associate, CAR-T Abecma CAR-T Summit West - NJ - US R1603830 Posted
Job in
Summit, Union County, New Jersey, 07902, USA
Listed on 2026-07-10
Listing for:
Bristol-Myers Squibb
Full Time
position Listed on 2026-07-10
Job specializations:
-
Manufacturing / Production
Manufacturing & Industrial Operations, Pharmaceutical Manufacturing, Production Associate / Production Line
Job Description & How to Apply Below
## Manufacturing Associate, CAR-T Abecma CAR-TSummit West - NJ - USFind out how well you match with this job
** 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:
*
* Position Title:
** Manufacturing Associate, CAR-T, Manufacturing Operations
** PURPOSE AND SCOPE OF POSITION:
** Manufactures 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:
** Wednesday
- Saturday (with e/o Wednesday off), Onsite Night Shift, 5 p.m.
- 5:30 a.m.Times are subject to change based on business demands.
** Responsibilities:
*** Manufacture human blood-derived cellular therapy products in accordance with SOPs and cGMP requirements.
* Perform cell culture maintenance and expansion, cell harvest, Isolation and cryopreservation activities.
* Execute aseptic processing activities, including: + Tube welding + Sampling + cell counts + Sterile connections + Material transfers
* Weigh and measure in-process materials to ensure required quantities are added or removed.
* Adhere to production schedules and support on-time manufacturing operations.
* Performs tasks for Cell Therapy products to support product Value Stream outputs according to Current Good Manufacturing Practices (cGMP’s) following the current, approved Standard Operating Procedures (SOPs) and Work Instructions (WIs).
* Communicate production deviations and support quality investigations when required.
* Work collaboratively within a cross-functional, team-based manufacturing environment.
* Perform activities within a designated manufacturing function as assigned.
* Perform additional manufacturing-related tasks as directed by management.
* Supports manual and electronic batch record executions, deviation investigations, and closure of CAPAs.
* Maintains timing according to the production schedule to ensure on-time logistics.
* Ensures all documentation is correct and addresses procedural/documentation errors expeditiously and effectively.
* Works in a team based, cross-functional environment to complete tasks required by shift schedule.
* Available to work OT when business requires.
* Willing to work staggered day shift hours.
* Records patient material handling data and information in a clear, concise, format according to proper GDPs.
** Knowledge and Skills
*** Basic understanding of: + Cell culture + Cryopreservation + Cell Expansion + Aseptic processing techniques + Laboratory techniques
* Knowledge and understanding of cGMP and FDA-regulated manufacturing environments.
* Technical writing and documentation skills.
* Proficiency in Microsoft Office applications.
* Foundational knowledge of: + Biology + Chemistry + Mathematics
* Strong teamwork and communication skills.
* Ability to work effectively in a fast-paced manufacturing environment.
* Inventory control and/or management.
** Minimum Requirements
**** Education and Experience
*** Bachelor's Degree;
** OR
* ** Associate degree/Medical Technical Degree with at least 2 years of…
Position Requirements
10+ Years
work experience
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