Senior Specialist, CAR-T Lifecycle Management
Bristol Myers Squibb
September 03, 2026
Remote friendly (Summit, NJ)
United States
Operations
Senior Specialist, CAR-T Lifecycle Management
Shifts Available:
- Monday–Friday, Hybrid Day Shift, 8 a.m.–5 p.m.
Responsibilities:
- Provide on-the-floor process support for manufacturing activities.
- Develop inputs into electronic batch record/process automation to advance manufacturing strategy.
- Participate on project teams (schedules, technical execution, presentations to stakeholders/senior management).
- Support change and process improvement initiatives; foster strong inter-team relationships.
- Interface with operations as process SME; monitor/analyze/optimize end-to-end process and permanently resolve production issues.
- Execute test plans and risk mitigation (e.g., root cause analysis, CAPAs).
- Organize, record, and maintain experimental data.
- Stay current with industry trends/standards (e.g., PDA, ISPE) and participate in best-practice forums.
- Assist with revisions to technical documentation (investigations, changes, SOPs, batch records).
- Interact with Validation, Development, Operations, QA, and Regulatory; attend routine plant operating meetings.
- Support health authority inspections; train and mentor junior associates.
Knowledge/Skills:
- Knowledge of cGMPs and multi-national biopharmaceutical regulations (cell therapy major plus).
- Single-use technologies, closed systems, cold chain/cryogenic technologies.
- Hands-on CAR-T or biopharma manufacturing/QC preferred; strong communication skills; strategic thinking.
Minimum Requirements:
- Bachelor’s degree (science/engineering preferred).
- 5+ years cGMP experience in Cell Therapy.
- 2+ years process engineering hands-on.
- 2+ years direct project management.
Working Conditions:
- 60–75% office; 25–40% manufacturing/lab; occasional NJ travel; flexibility for extended hours/weekends/holidays.
Benefits/Compensation (as stated):
- Base pay range: $81,920–$99,271 (Summit West, NJ, US). Eligible for comprehensive benefits and (U.S. exempt) Flexible Time Off plus 11 paid holidays.
Application Instructions:
- Apply via BMS careers; reference requisition R1604191.
Shifts Available:
- Monday–Friday, Hybrid Day Shift, 8 a.m.–5 p.m.
Responsibilities:
- Provide on-the-floor process support for manufacturing activities.
- Develop inputs into electronic batch record/process automation to advance manufacturing strategy.
- Participate on project teams (schedules, technical execution, presentations to stakeholders/senior management).
- Support change and process improvement initiatives; foster strong inter-team relationships.
- Interface with operations as process SME; monitor/analyze/optimize end-to-end process and permanently resolve production issues.
- Execute test plans and risk mitigation (e.g., root cause analysis, CAPAs).
- Organize, record, and maintain experimental data.
- Stay current with industry trends/standards (e.g., PDA, ISPE) and participate in best-practice forums.
- Assist with revisions to technical documentation (investigations, changes, SOPs, batch records).
- Interact with Validation, Development, Operations, QA, and Regulatory; attend routine plant operating meetings.
- Support health authority inspections; train and mentor junior associates.
Knowledge/Skills:
- Knowledge of cGMPs and multi-national biopharmaceutical regulations (cell therapy major plus).
- Single-use technologies, closed systems, cold chain/cryogenic technologies.
- Hands-on CAR-T or biopharma manufacturing/QC preferred; strong communication skills; strategic thinking.
Minimum Requirements:
- Bachelor’s degree (science/engineering preferred).
- 5+ years cGMP experience in Cell Therapy.
- 2+ years process engineering hands-on.
- 2+ years direct project management.
Working Conditions:
- 60–75% office; 25–40% manufacturing/lab; occasional NJ travel; flexibility for extended hours/weekends/holidays.
Benefits/Compensation (as stated):
- Base pay range: $81,920–$99,271 (Summit West, NJ, US). Eligible for comprehensive benefits and (U.S. exempt) Flexible Time Off plus 11 paid holidays.
Application Instructions:
- Apply via BMS careers; reference requisition R1604191.