Specialist, CAR-T Supply Chain PPS
Bristol Myers Squibb
August 13, 2026
Remote friendly (Summit, NJ)
United States
Operations
Position Summary
- Schedule operations supporting clinical and commercial CAR-T manufacturing at the Summit West site, collaborating across internal/external functions to ensure on-time fulfillment of final product.
Duties & Responsibilities
- Create, maintain, and publish finite schedules for operations (apheresis/PBMC/CMAT receipt, material kitting, cell processing, media manufacturing).
- Serve as point of contact for Manufacturing Operations and Value Stream functions (ECQ, Facilities, Quality) to support continuity and address issues.
- Complete ERP lot creation and batch record request tasks for weekly document issuance.
- Collaborate with cross-functional partners (OpEx, IT, Materials Management, Master Data Management, Manufacturing Technical Services) on implementations, continuous improvement, and software/dashboard development.
- Perform other tasks as assigned.
Qualifications
Knowledge/Skills/Abilities (required/preferred)
- Understanding of cell culture, cryopreservation, purification, and aseptic processing/lab technique.
- Knowledge of cGMP/pharmaceutical regulations.
- Proficient in planning/ERP systems (SAP) and analytics tools; advanced MS Office.
- Strong written/verbal communication; presentation development/delivery.
- Identify continuous improvement opportunities; work independently and in a team; solve routine/complex problems.
- Provide on-call support for emergent issues.
Education & Experience
- Bachelor’s degree required.
- 2–3+ years relevant experience (regulated pharmaceutical manufacturing preferred).
- 1+ year production scheduler/planner.
- 1+ year ERP support (preferably Oracle or SAP).
Compensation & Benefits (as stated)
- $33.49–$40.59 per hour (Summit West, NJ). Health, wellbeing, and financial protection benefits; paid time off.
Travel
- Less than 10%.
- Schedule operations supporting clinical and commercial CAR-T manufacturing at the Summit West site, collaborating across internal/external functions to ensure on-time fulfillment of final product.
Duties & Responsibilities
- Create, maintain, and publish finite schedules for operations (apheresis/PBMC/CMAT receipt, material kitting, cell processing, media manufacturing).
- Serve as point of contact for Manufacturing Operations and Value Stream functions (ECQ, Facilities, Quality) to support continuity and address issues.
- Complete ERP lot creation and batch record request tasks for weekly document issuance.
- Collaborate with cross-functional partners (OpEx, IT, Materials Management, Master Data Management, Manufacturing Technical Services) on implementations, continuous improvement, and software/dashboard development.
- Perform other tasks as assigned.
Qualifications
Knowledge/Skills/Abilities (required/preferred)
- Understanding of cell culture, cryopreservation, purification, and aseptic processing/lab technique.
- Knowledge of cGMP/pharmaceutical regulations.
- Proficient in planning/ERP systems (SAP) and analytics tools; advanced MS Office.
- Strong written/verbal communication; presentation development/delivery.
- Identify continuous improvement opportunities; work independently and in a team; solve routine/complex problems.
- Provide on-call support for emergent issues.
Education & Experience
- Bachelor’s degree required.
- 2–3+ years relevant experience (regulated pharmaceutical manufacturing preferred).
- 1+ year production scheduler/planner.
- 1+ year ERP support (preferably Oracle or SAP).
Compensation & Benefits (as stated)
- $33.49–$40.59 per hour (Summit West, NJ). Health, wellbeing, and financial protection benefits; paid time off.
Travel
- Less than 10%.