Senior Manager, PV Quality Risk Management & Deviations at Bristol Myers Squibb

Setup: Hybrid
Type: Full-time
Level: senior

Description

Bristol Myers Squibb is hiring a Senior Manager, PV Quality Risk Management & Deviations to lead strategic assessment, investigation, closure, trending, root cause analysis, and cross-functional management of high-impact GVP deviations, CAPA, and quality risk management activities within pharmacovigilance. The role partners with global process owners, medical leads, and third parties to strengthen compliance, maintain QMS documentation, support inspections, and drive training and enterprise-wide adoption of quality practices. The position is aligned to BMS’s site-essential/site-by-design occupancy structure and may be hybrid depending on role assignment.

Required Skills

Deviation management
Root cause analysis
Risk management
CAPA
QMS
GVP inspections

Additional Information

Required Previous Experiences: Senior-level experience in quality risk management and deviation oversight
Experience supporting health authority and business partner inspections
Cross-functional pharmacovigilance and quality collaboration experience
Preferred Qualifications: Experience with structured root cause analysis methods
Knowledge of global regulatory and quality standards
Training and facilitation skills
Vendor and third-party quality assessment experience
Local process ownership and leadership experience

About Bristol Myers Squibb

Bristol Myers Squibb

biopharmaNew York, NY, US

Learn more about Wendy Short Bartie, Executive Vice President, Corporate Affairs, is responsible for advancing our company strategy through strategic communications, corporate social responsibility, corporate marketing and brand reputation, and patient advocacy.