Lead Quality Specialist

GE HealthCare Technologies

Base: $89,600.00-$134,400.00 annual; bonus/equity:...
Onsite
Bachelor's degree or 4 years relevant experience
Hands-on quality management system (qms) management
Regulated manufacturing environment experience
GE HealthCare Technologies is seeking a Lead Quality Specialist to oversee its Quality Management System and ensure compliance with industry standards. The ideal candidate should have significant experience in regulated environments, particularly in medical devices, and demonstrate strong collaboration and communication skills

Job Summary

  • The role involves developing and maintaining systems to ensure fulfillment of internal and external quality requirements for medical technology products.
  • Candidates will drive a quality culture by managing compliance activities, metrics, and ensuring process effectiveness in a fast-paced team environment.
  • GE HealthCare offers a competitive benefits package including medical, dental, vision, 401(k) matching, and performance-based incentive compensation.

Matching Summary

Match Score: 85

GE HealthCare Technologies is seeking a Lead Quality Specialist to oversee its Quality Management System and ensure compliance with industry standards. The ideal candidate should have significant experience in regulated environments, particularly in medical devices, and demonstrate strong collaboration and communication skills.

Salary

Base: $89,600.00-$134,400.00 Annual; Bonus/Equity: Performance based incentive compensation available; Benefits: Medical, dental, vision, 401(k), life, disability insurance

Skills & Requirements

Must-have

  • Bachelor's Degree or 4 years relevant experience
  • Hands-on Quality Management System (QMS) management
  • Regulated manufacturing environment experience
  • ISO standards compliance knowledge
  • Internal audit and document control expertise

Nice-to-have

  • Clean room or semiconductor environment exposure
  • Complex product line support experience
  • Cross-functional collaboration skills
  • Process improvement initiative leadership
  • Strong technical writing abilities

Key Requirements

  • Bachelor's Degree or minimum 4 years in Quality Management
  • Experience with ISO 13485 and medical device QMS
  • Proficiency in CAPA, root cause analysis, and audits
  • Legal authorization to work in the United States
  • No visa sponsorship provided

Work Rights

Must be legally authorized to work in the US

Tailored Resume

Cover Letter