The Associate Director will drive the strategy for Inspection Readiness and execute compliance and inspection support programs in a matrixed organization
Job Summary
The Associate Director will drive the strategy for Inspection Readiness and execute compliance and inspection support programs in a matrixed organization.
Key responsibilities include monitoring global regulatory inspection outcomes, conducting enterprise reviews of regulatory interactions, and performing on-site or remote inspection readiness assessments.
Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.
Matching Summary
The Associate Director will drive the strategy for Inspection Readiness and execute compliance and inspection support programs in a matrixed organization.
Salary
Base: $163,850 - $212,438; 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
global auditing procedures
regulatory inspection outcomes
risk-based approach
quality systems principles
Nice-to-have
innovation and adaptability
collaboration and influence
patient impact
continuous improvement
Key Requirements
7+ years in Biopharm/Pharmaceutical industry
Bachelor’s degree in Natural Science, Pharmacy, or related fields
Minimum 5 years as FDA CSO or similar role (2015-2025)
Demonstrated negotiation, risk management, relationship management, and conflict resolution skills