Director, Central Quality Audit

GEHC

Multiple Locations
Base: $142,400.00-$213,600.00 annual; bonus/equity...
Global pv audit strategy development
Regulatory compliance management
Audit operations oversight
GE HealthCare is a leading global medical technology and digital solutions innovator with a mission to improve lives in the moments that matter

Job Summary

  • GE HealthCare is a leading global medical technology and digital solutions innovator with a mission to improve lives in the moments that matter.
  • The role involves owning the global Pharmacovigilance audit program, managing audit operations, supporting regulatory inspections, and leading a team of auditors.
  • GE HealthCare offers a competitive benefits package, career development opportunities, and a culture that fosters care, collaboration, and support.

Matching Summary

GE HealthCare is a leading global medical technology and digital solutions innovator with a mission to improve lives in the moments that matter.

Salary

Base: $142,400.00-$213,600.00 Annual; Bonus/Equity: Performance based incentive compensation including cash bonus and/or long term incentives; Benefits: Medical, dental, vision, paid time off, 401(k), life, disability, accident insurance, tuition reimbursement

Skills & Requirements

Must-have

  • Global PV audit strategy development
  • Regulatory compliance management
  • Audit operations oversight
  • Quality Management System (QMS) expertise
  • Team leadership and development
  • Cross-functional collaboration

Nice-to-have

  • Experience with Veeva and TrackWise
  • Health authority inspection experience
  • Lean and Six Sigma methodologies
  • Strong conflict-resolution skills
  • Ability to influence policy and strategy
  • Exceptional communication skills

Key Requirements

  • Minimum 5 years people leadership experience
  • Qualified Lead Auditor certification
  • Master’s degree with 5+ years in pharmacovigilance or pharmaceutical industry or Bachelor’s with 10+ years experience
  • 5+ years driving global quality compliance programs
  • Experience with pharmaceutical and medical device QMS and regulatory requirements
  • Ability to travel globally up to 30%

Work Rights

Must be legally authorized to work in the United States

Tailored Resume

Cover Letter