Sr Director, Japan External Supply Head

Bristol Myers Squibb

Japan
On-site
Cell therapy external supply
Cdmo partnership management
Clinical and commercial product delivery
Bristol Myers Squibb is seeking a Sr Director, Japan External Supply Head, to oversee the global delivery of clinical and commercial products in cell therapy manufactured by CDMOs in Japan. The role requires extensive experience in biologics or cell therapy manufacturing, strong leadership skills, and fluency in Japanese and English

Job Summary

  • The head of Japan cell therapy external supply is accountable for global delivery of clinical and commercial products manufactured by contract development and manufacturing organizations (CDMOs) located in Japan.
  • Leading a multidisciplinary and cross-functional matrix team, the role is accountable for strategic partnership management to implement, achieve and maintain reliable supply and performance within the external network.
  • Accountable for > $100M of spend, driving financial stewardship and sustainable cost reduction without compromising safety, quality or supply is a key challenge to be met.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Sr Director, Japan External Supply Head, to oversee the global delivery of clinical and commercial products in cell therapy manufactured by CDMOs in Japan. The role requires extensive experience in biologics or cell therapy manufacturing, strong leadership skills, and fluency in Japanese and English.

Skills & Requirements

Must-have

  • cell therapy external supply
  • CDMO partnership management
  • clinical and commercial product delivery
  • quality and regulatory compliance
  • supply chain optimization
  • financial stewardship

Nice-to-have

  • strategic partnership development
  • cross-functional matrix team leadership
  • continuous improvement initiatives
  • business process development

Key Requirements

  • 10+ years of experience in biopharmaceutical manufacturing or supply chain
  • Strong technical expertise in biologics or cell therapy commercial manufacturing
  • Experience with technology transfer and/or start-up phase
  • Exposure to PMDA, FDA, EMA regulatory agencies
  • Demonstrated success negotiating complex supply and toll manufacturing agreements with CDMOs
  • Japanese/English required for role based in Japan

Work Rights

Not specified

Tailored Resume

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