Associate Director, Audit Strategy And Vendor Quality

Bristol Myers Squibb

Princeton, NJ, US
Base: $163,210 - $197,770; bonus/equity: + incenti...
Hybrid (50% onsite)
8+ years in quality assurance or regulated clinical development
Strong gcp knowledge and ich e6(r3) expertise
Hands-on experience executing risk-based audits
Bristol Myers Squibb is seeking an Associate Director for Audit Strategy and Vendor Quality to develop and execute risk-based audit strategies, ensuring high-quality standards in R&D processes and vendor management. The role requires extensive experience in Quality Assurance and regulatory compliance, as well as strong communication and project management skills

Job Summary

  • This role supports the development and execution of risk-based audit strategies across Therapeutic Areas, R&D processes, and external vendors to ensure patient safety and product quality.
  • The Associate Director will lead vendor due diligence, oversee quality agreements, and manage third-party risk controls while ensuring inspection readiness for health authorities.
  • Bristol Myers Squibb offers competitive benefits including flexible time off, comprehensive health coverage, and a supportive culture focused on transforming patients' lives through science.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director for Audit Strategy and Vendor Quality to develop and execute risk-based audit strategies, ensuring high-quality standards in R&D processes and vendor management. The role requires extensive experience in Quality Assurance and regulatory compliance, as well as strong communication and project management skills.

Salary

Base: $163,210 - $197,770; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • 8+ years in Quality Assurance or regulated clinical development
  • Strong GCP knowledge and ICH E6(R3) expertise
  • Hands-on experience executing risk-based audits
  • Vendor oversight and Third-Party Risk Management (TPRM)
  • Experience supporting regulatory inspections and submission readiness

Nice-to-have

  • Innovative mindset for improving audit execution
  • Exposure to data analytics or data science tools
  • Experience with M&A due diligence activities
  • Ability to translate findings into actionable CAPAs
  • Strong project management skills in a global environment

Key Requirements

  • B.S. or M.S. in scientific, health, or quality-related discipline
  • 8+ years of experience in Quality Assurance or regulated clinical development
  • Expertise in ICH/GCP guidelines and clinical research processes

Work Rights

Not specified

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