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Executive Director, Internal Site & ExM Supply Chain, Cell Therapy Supply Chain

Bristol Myers Squibb
June 30, 2026
Remote friendly (New Brunswick, NJ)
United States
Operations
Position Summary
Reporting to the Vice President, Cell Therapy Supply Chain, the Executive Director, Internal Site & ExM Supply Chain is accountable for the strategic development and operational execution of Cell Therapy Supply Chain across BMS’s global internal drug product manufacturing sites and external manufacturing partners.

Key Responsibilities
- Lead end-to-end supply chain execution (planning, scheduling, inventory, materials management) across internal CT sites and ExM CMOs.
- Manage supply chain performance (service levels, cycle time, inventory effectiveness, demand variability responsiveness) and plan-vs-actual performance.
- Ensure predictable delivery, issue escalation, and continuous strategy updates for short- and long-term results.
- Own daily warehouse operations (kitting, staging, shipping) in compliance with GDP/GMP, environmental, health, and safety standards.
- Serve as single point of contact for internal sites and ExM CMOs across CT Drug Product Operations / ExM leadership forums; drive S&OP input, Integrated Planning support, and Network Plan/S&OP integration.
- Lead capacity/staffing and contingency planning to meet commercial and clinical commitments.
- Prepare/monitor annual budget and quarterly projections; set site/ExM goals and KPIs.
- Ensure master data maintenance, training documentation/procedures, compliance with supply chain/transportation/customs/trade requirements, onboarding/succession, and capability enhancements.

Qualifications & Experience
- B.S./B.A. in supply chain management, science, and/or engineering; MBA/advanced supply chain credential (e.g., APICS/CSCP) strongly preferred.
- 15+ years supply chain management and planning experience in biotech/pharma/consumer products; demonstrated site operations/supply chain leadership.
- Experience managing teams and influencing senior leaders; strong analytical, communication, problem-solving, and strategic planning skills.
- Knowledge of cGMP, FDA, and other regulatory requirements; ability to work in a matrix environment.

Compensation & Benefits (if applicable)
- Compensation range: $267,330–$323,945.
- Health coverage (medical/pharmacy/dental/vision); wellbeing support; 401(k) and life/disability/insurance benefits; paid time off (flexible time off or annual vacation depending on location/role).