Offer summary
Qualifications:
Bachelor’s degree in Science, Engineering or related field; Master's degree is preferred, 12+ years of Quality Assurance/Regulatory experience in medical device manufacturing, with at least 10 years in management.
Key responsabilities:
- Provide Performance Status reports to Executive Leadership
- Lead quality and regulatory systems across sites, manage high-priority projects and customer relationships
- Streamline Quality processes and drive improvements based on analysis
- Hire, train, and guide direct reports and create development plans