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

Bristol Myers Squibb
July 02, 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.
Direct leadership of Site Supply Chain Leads across Bothell, Summit, Devens, and Leiden, and External Manufacturing (ExM) Supply Chain Lead(s).

Key Responsibilities
- Provide leadership and strategic direction across planning, scheduling, inventory control, warehousing, and logistics for CT internal sites and ExM CMOs.
- Own supply chain performance management (service levels, cycle time, inventory effectiveness, and demand variability responsiveness).
- Ensure predictable delivery, issue escalation, and plan vs. actual performance.
- Serve as single point of contact for internal sites and ExM CMOs on CT Drug Product Operations and ExM leadership teams.
- Manage daily warehouse operations (kitting, staging, shipping) in compliance with GDP, GMP, and relevant EHS standards.
- Prepare and monitor annual budgets and quarterly projections; develop site and ExM CMO Supply Chain goals/KPIs.
- Ensure capacity, staffing, contingency planning, master data maintenance, training documentation, and supply chain compliance.
- Partner with CTSC LT; support integrated planning/S&OP process integration; communicate decisions and supply impacts to stakeholders.

Qualifications & Experience
- B.S./B.A. in supply chain management, science, and/or engineering; MBA or advanced degree and/or supply chain certifications (e.g., APICS/CSCP) strongly preferred.
- 15+ years supply chain management and planning experience in global/multi-plant biopharma (or similar).
- Demonstrated site operations/supply chain leadership, team management, senior stakeholder influence, analytical and strategic problem-solving.
- Working knowledge/exposure to cGMP, FDA, and other regulatory requirements.

Required Skills/Competencies
- Strong communication and presentation (oral/written), negotiation/influencing without authority, coaching/mentoring, and ability to operate in a matrix environment.

Compensation/Benefits (if explicitly stated)
- Compensation range: $267,330 - $323,945.

Application Instructions
- Apply even if your experience doesn’t perfectly match; the posting encourages applications regardless.