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Specialist, CAR-T Supply Chain PPS
Job in
Summit, Union County, New Jersey, 07902, USA
Listed on 2026-08-07
Listing for:
Bristol-Myers Squibb
Full Time
position Listed on 2026-08-07
Job specializations:
-
Manufacturing / Production
Manufacturing & Industrial Operations
Job Description & How to Apply Below
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: .Specialist, CAR-T Production Planning and Scheduling Department:
Breyanzi and Abecma Value Stream
Location:
Summit, NJ Position Summary The primary responsibility of this role is to schedule operations supporting clinical and commercial CAR-T manufacturing at the Summit West site. The role will require significant collaboration across internal and external functions to ensure on-time fulfillment of final product. The ideal candidate will have a demonstrated ability to balance multiple competing priorities, participate in projects, and follow Scheduling best practices.
Duties & Responsibilities Create, maintain, and publish detailed finite schedules for operations including apheresis and PBMC/CMAT receipt, material kitting, cell processing, and media manufacturing.
Serve as point of contact for the Manufacturing Operations organization and Value Stream functions including ECQ, Facilities, and Quality to provide support, facilitate operational continuity, and address issues as they arise.
Complete all ERP lot creation and batch record request tasks required for weekly document issuance.
Collaborate with cross-functional business partners such as OpEx, IT, Materials Management, Master Data Management, and Manufacturing Technical Services on system implementations, continuous improvement projects, and software/dashboard development.
Perform other tasks as assigned.
Reporting To:
Associate Director, Value Stream Planning Qualifications Knowledge , Skills & Abilities:
Understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique
Knowledge of cGMP/Pharmaceutical regulations
Proficient in planning/ERP systems (SAP) and analytics tools
Advanced proficiency in MS Office applications
Strong written and verbal communication skills
Proficient presentation development and delivery skills
Ability to identify continuous improvement opportunities
Ability to work independently and as part of a team Ability to solve routine and complex problems
Ability to provide on-call support for emergent issues
Education & Experience:
Bachelor's degree required2–3+ years of relevant work experience, preferably in a regulated pharmaceutical manufacturing environment1+ years of experience as a production scheduler or planner1+ years of experience supporting ERP systems (preferably Oracle or SAP)
An equivalent combination of education, experience, and training may substitute
Working Conditions Intermittent walking and sitting; ability to sit or stand for extended periods may be necessary
Physical dexterity sufficient to use computers and documentation
Sufficient vision and hearing capability to work in the job environment
Ability to lift up to 25 pounds
Must be able to work around laboratories and controlled, enclosed, restricted areas
Cleanroom garments and PPE required in designated areas
Makeup, gum, nail polish, or other potential microbial sources are prohibited in restricted areas
Clean room environment includes assigned pressure and temperature conditions; exposure to reagents, chemicals, and sanitization agents is expected
Routine exposure to human blood components
Designated areas may prohibit food and outside materials (e.g., cell phones, tablets)
Travel:
Less than 10%
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