Associate Director, Audit Strategy And Vendor Quality

Bristol Myers Squibb

Princeton, NJ, US
Base: $163,210 - $197,770; bonus/equity: + incenti...
Hybrid (50% onsite)
Risk-based audit strategies
Vendor quality oversight
Ich/gcp knowledge
Bristol Myers Squibb is seeking an Associate Director of Audit Strategy and Vendor Quality to lead the development and execution of audit strategies in clinical development and vendor oversight. The role emphasizes risk-based auditing, vendor quality management, and regulatory readiness, contributing to the company's mission of transforming patients' lives through innovative science

Job Summary

  • This role supports the development and execution of risk-based audit strategies across Therapeutic Areas, R&D processes, and external vendors.
  • The Associate Director will lead and support maintaining and applying the vendor quality management framework such as vendor oversight plans, quality agreements, and governance metrics.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits, services and programs.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director of Audit Strategy and Vendor Quality to lead the development and execution of audit strategies in clinical development and vendor oversight. The role emphasizes risk-based auditing, vendor quality management, and regulatory readiness, contributing to the company's mission of transforming patients' lives through innovative science.

Salary

Base: $163,210 - $197,770; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Risk-based audit strategies
  • Vendor quality oversight
  • ICH/GCP knowledge
  • Regulatory inspection readiness
  • Quality risk management

Nice-to-have

  • Data analytics for quality
  • Continuous improvement initiatives
  • Cross-functional collaboration
  • Innovative mindset
  • M&A due diligence support

Key Requirements

  • 8+ years in Quality Assurance or regulated clinical development
  • Hands-on experience executing risk-based audits
  • Experience supporting regulatory inspections
  • B.S. or M.S. in a scientific, health, or quality-related discipline

Work Rights

Not specified

Tailored Resume

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