Associate Director, Global Quality System & Compliance

Revolution Medicines

Redwood City, California, United States
Base: $186,000 - $233,000 usd; bonus/equity: compe...
On-site
Global quality management system leadership
Gxp regulations fda ema pmda knowledge
10+ years pharmaceutical quality experience
Revolution Medicines is seeking an Associate Director of Global Quality System & Compliance to lead the scaling and globalization of their Quality Management System (QMS) in the field of clinical oncology. The ideal candidate will have extensive experience in quality within the pharmaceutical or biotechnology industry and will play a critical role in ensuring compliance and operational efficiency across global sites

Job Summary

  • The role involves providing strategic and operational leadership to scale and globalize the Quality Management System across international regions.
  • Candidates must ensure inspection readiness and lead support for global health authority inspections including FDA, EMA, and PMDA.
  • The position requires establishing governance for electronic quality systems like Veeva Vault while maintaining global consistency.

Matching Summary

Match Score: 85

Revolution Medicines is seeking an Associate Director of Global Quality System & Compliance to lead the scaling and globalization of their Quality Management System (QMS) in the field of clinical oncology. The ideal candidate will have extensive experience in quality within the pharmaceutical or biotechnology industry and will play a critical role in ensuring compliance and operational efficiency across global sites.

Salary

Base: $186,000 - $233,000 USD; Bonus/Equity: Competitive equity awards included; Benefits: Robust benefits and learning opportunities provided

Skills & Requirements

Must-have

  • Global Quality Management System leadership
  • GxP regulations FDA EMA PMDA knowledge
  • 10+ years pharmaceutical quality experience
  • Regulatory inspection readiness support
  • Electronic QMS systems like Veeva Vault

Nice-to-have

  • Experience transforming global QMS in growth phase
  • Commercial product launch lifecycle management
  • Culture of continuous improvement championing
  • Cross-functional stakeholder influence skills

Key Requirements

  • Bachelor's degree in Life Sciences or related field
  • Minimum 10 years experience in pharmaceutical/biotech quality
  • Proven track record with global regulatory filings and approvals

Work Rights

Not specified

Tailored Resume

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