Senior Director, External Manufacturing & Supply Strategy

Teva

Haarlem

On-site

EUR 150,000 - 190,000

Full time

6 days ago
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Benefits offered by this job

Flexible working schedules
Generous annual leave
Health support programs
Career development via Twist platform

Job summary

Teva seeks a Senior Director, Supplier Relationship Management, to lead an external manufacturing site network ensuring reliable patient supply and regulatory compliance. The role oversees cross-functional partners and drives manufacturing readiness, process improvements, and lifecycle management across multiple sites.

The incumbent collaborates with Quality, Regulatory, MSAT, and Finance to optimize costs and performance, while sustaining a culture of accountability and continuous improvement

Qualifications

  • 15+ years of progressive biologics experience in manufacturing or related roles.
  • 10+ years leadership in biologics manufacturing including external manufacturing/CDMO management.
  • Strong knowledge of cGMP, manufacturing science, and process validation.
  • Experience supporting regulatory filings and inspections.

Responsibilities

  • Lead end-to-end manufacturing operations across external partners to ensure reliable patient supply.
  • Establish governance, metrics, and management review programs for performance.
  • Identify supplier risks and implement proactive mitigation strategies.
  • Drive continuous improvement and cost optimization in external manufacturing.
  • Collaborate with Quality, Regulatory, and MSAT to maintain cGMP compliance.
  • Develop long-term supplier strategies and capital planning.

Skills

Cross-functional leadership
cGMP knowledge
Regulatory filings
Contract manufacturing
Stakeholder engagement
Financial acumen
Change management
Global collaboration

Education

Bachelor's degree in Engineering, Life Sciences, Biotechnology
Master's degree or MBA preferred

Job description

Teva seeks a Senior Director, Supplier Relationship Management, to lead an external manufacturing site network ensuring reliable patient supply and regulatory compliance. The role oversees cross-functional partners and drives manufacturing readiness, process improvements, and lifecycle management across multiple sites.

The incumbent collaborates with Quality, Regulatory, MSAT, and Finance to optimize costs and performance, while sustaining a culture of accountability and continuous improvement

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