Job Summary

• The Associate Director will support BMS’ GMP/GDP Inspection Readiness strategy by supporting on-site and remote assessments of BMS internal and external sites, providing real-time support, based on a risk-based approach.
• This role will monitor and assess global regulatory inspection outcomes, enforcement actions, quality and compliance metrics, and external signals, leveraging these insights to anticipate regulatory expectations, shape enterprise-wide inspection readiness strategies, and drive proactive, continuous improvement.
• 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

Salary

Base: $175,310 - $212,438 (Devens); $163,850 - $198,543 (New Brunswick/Princeton); 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

Key Requirements

• 7+ years in Biopharm/Pharmaceutical industry
• Bachelor’s degree in Natural Science, Pharmacy, or related fields
• Minimum of 5 years' experience as a CSO
• Worked for US FDA within past 10 years
• Demonstrated negotiation, risk management, relationship management and conflict resolution skills

Work Rights