Director, Quality & Regulatory Business Development-2

GE HealthCare Technologies

Not specified; not specified; competitive compensa...
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Master's degree in medical device industry
5 years experience in medical device qms
Fda 21 cfr part 820 and iso 13485 knowledge
** GE HealthCare Technologies is seeking a Director of Quality & Regulatory Business Development with expertise in the medical device industry to manage and improve business development capabilities. The ideal candidate should have significant experience with quality management systems and regulatory requirements, alongside strong leadership and project management skills. **

Job Summary

  • The role involves managing, analyzing, and improving business development capabilities while ensuring products meet specified standards.
  • Candidates must interpret internal and external business challenges to recommend best practices that improve products, processes, or services.
  • GE HealthCare offers a great work environment with professional development and challenging careers for those who can drive global quality compliance programs.

Matching Summary

Match Score: 75

** GE HealthCare Technologies is seeking a Director of Quality & Regulatory Business Development with expertise in the medical device industry to manage and improve business development capabilities. The ideal candidate should have significant experience with quality management systems and regulatory requirements, alongside strong leadership and project management skills. **

Salary

Not specified; Not specified; Competitive compensation mentioned

Skills & Requirements

Must-have

  • Master's degree in medical device industry
  • 5 years experience in medical device QMS
  • FDA 21 CFR Part 820 and ISO 13485 knowledge

Nice-to-have

  • ASQ certification CQE or CQA preferred
  • Lean Six Sigma Green Belt or Black Belt
  • Ability to travel domestically and internationally

Key Requirements

  • Minimum 5 years medical device industry experience
  • Experience with FDA 21 CFR Part 820 regulations
  • Experience with ISO 13485 regulatory requirements
  • No visa sponsorship provided for this role

Work Rights

Must be legally authorized to work in the United States

Tailored Resume

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