Senior Manager, Pv Process Quality Lead

Bristol Myers Squibb

Warsaw, Poland
Base: zł227,340 - zł275,484; bonus/equity: + incen...
50% onsite
Gvp deviation investigation
Root cause analysis
Qms documentation authoring
The Patient Safety Quality Management (SQM) organization supports shaping tomorrow's healthcare landscape through forward-thinking third party and internal compliance, transformative quality & procedural initiatives, PSMF excellence, facilitating engagement with PV Regulatory Intelligence, and dynamic external collaborations

Job Summary

  • The Patient Safety Quality Management (SQM) organization supports shaping tomorrow's healthcare landscape through forward-thinking third party and internal compliance, transformative quality & procedural initiatives, PSMF excellence, facilitating engagement with PV Regulatory Intelligence, and dynamic external collaborations.
  • Shapes and directs strategic assessment, investigation, and closure of high-impact GVP deviations, influencing remediation priorities and organizational risk management.
  • 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

The Patient Safety Quality Management (SQM) organization supports shaping tomorrow's healthcare landscape through forward-thinking third party and internal compliance, transformative quality & procedural initiatives, PSMF excellence, facilitating engagement with PV Regulatory Intelligence, and dynamic external collaborations.

Salary

Base: zł227,340 - zł275,484; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Not specified

Skills & Requirements

Must-have

  • GVP deviation investigation
  • Root cause analysis
  • QMS documentation authoring
  • Cross-functional partnerships
  • PV System Master File (PSMF)
  • PV projects and initiatives

Nice-to-have

  • Transformative quality initiatives
  • Forward-thinking compliance
  • Culture of quality and continuous improvement
  • Elevating team expertise
  • Dynamic external collaborations

Key Requirements

  • University degree in health or life sciences, or nursing qualification
  • Minimum 5 years' experience in pharmaceutical industry
  • 2-3 years in Pharmacovigilance or related field
  • Proven leadership in quality management or compliance
  • Experience managing cross-functional teams

Work Rights

Not specified

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