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Summary
About the Role
About You
- Master’s Degree and a minimum of 7 years’ experience in the medical device industry; or Bachelor's Degree and a minimum of 9 years’ experience; or High School Diploma with a minimum of 13 years' experience.
- Minimum of 5 years’ experience driving Global programs to resolve quality compliance issues.
- Experience with Pharma QMS requirements and regulatory requirements including FDA 21 CFR Part 211 & 212, Eudralex and PICS.
- Demonstrated ability to lead programs/projects and established project management skills.
- ASQ Certification (CQE, CQA, etc.) and/or Lean Certification (green belt, black belt).
- Strong oral and written communication skills in English.
Benefits
- Competitive salary range of $139k–$209k annually.
- Comprehensive benefits package including medical, dental, vision, paid time off, and a 401(k) plan.
- Opportunities for professional development and career advancement.
Every day millions of people feel the impact of our intelligent devices, advanced analytics and artificial intelligence. As a leading global medical technology and digital solutions innovator, GE HealthCare enables clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications and services, supported by its Edison intelligence platform. With over 100 years of healthcare industry experience and around 50,000 employees globally, the company operates at the center of an ecosystem working toward precision health, digitizing healthcare, helping drive productivity and improve outcomes for patients, providers, health systems and researchers around the world. We embrace a culture of respect, transparency, integrity and diversity and we work to create a world where healthcare has no limits.