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 in Princeton, NJ, who will be responsible for developing and executing risk-based audit strategies across various therapeutic areas and external vendors. The ideal candidate will have extensive experience in Quality Assurance and clinical development, with a focus on vendor oversight and regulatory compliance
Job Summary
This role supports the development and execution of risk-based audit strategies across Therapeutic Areas, R&D processes, and external vendors.
The position involves leading vendor due diligence, ongoing quality oversight, and implementing Third-Party Risk Management controls aligned with governance frameworks.
Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being programs, and flexible time off options.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking an Associate Director for Audit Strategy and Vendor Quality in Princeton, NJ, who will be responsible for developing and executing risk-based audit strategies across various therapeutic areas and external vendors. The ideal candidate will have extensive experience in Quality Assurance and clinical development, with a focus on vendor oversight and regulatory compliance.
Salary
Base: $163,210 - $197,770; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Health coverage, 401(k), paid time off, and wellbeing support
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
Experience with vendor oversight and TPRM activities
Proven track record supporting regulatory inspections
Nice-to-have
Exposure to data analytics or data science tools
Innovative mindset for improving audit processes
Experience with M&A due diligence activities
Ability to translate findings into actionable CAPAs
Strong project management skills in global environment
Key Requirements
B.S. or M.S. in scientific, health, or quality-related discipline
8+ years of relevant experience in Quality Assurance
Expertise in ICH/GCP and clinical research processes