Offer summary
Qualifications:
Bachelor's in Science, Engineering or technical discipline, Minimum 12+ years in quality assurance/regulatory for medical devices, In-depth medical device quality management experience, 10 years of management experience with multi-site responsibility, Master's degree preferred.
Key responsabilities:
- Manage quality and regulatory systems across sites
- Act as principal escalation contact for quality issues
- Streamline quality processes for consistency
- Drive use of QA/RA KPIs for performance improvement
- Develop best practices from site assessments and trends