Associate Director, Audit Strategy And Vendor Quality

Bristol Myers Squibb

Princeton, NJ, US
Base: $163,210 - $197,770; bonus/equity: + incenti...
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Risk-based audit strategies
Vendor quality oversight
Gcp and clinical research processes
** Bristol Myers Squibb is seeking an Associate Director for Audit Strategy and Vendor Quality to develop and execute risk-based audit strategies across various therapeutic areas. The role involves leading audits, vendor oversight, and ensuring compliance with regulatory standards while fostering a collaborative work environment. **

Job Summary

  • The Associate Director, Audit Strategy and Vendor Quality supports the development and execution of risk-based audit strategies across Therapeutic Areas, R&D processes, and external vendors.
  • This role focuses on operationalizing risk-based audit plans, delivering effective audit execution, supporting quality investigations and CAPA management, as well as proactively identifying and escalating quality risks.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking an Associate Director for Audit Strategy and Vendor Quality to develop and execute risk-based audit strategies across various therapeutic areas. The role involves leading audits, vendor oversight, and ensuring compliance with regulatory standards while fostering a collaborative work environment. **

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
  • GCP and clinical research processes
  • Quality investigations and CAPA management
  • Third-Party Risk Management (TPRM)

Nice-to-have

  • Data analytics and data science
  • Continuous improvement initiatives
  • Innovative mindset
  • Global collaboration

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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