Offer summary
Qualifications:
Bachelor's in Science or Engineering, 12+ years in quality assurance/regulatory for medical devices, 10 years management experience with multi-site responsibility, In-depth knowledge of medical device quality management systems, Master's degree preferred.
Key responsabilities:
- Manage quality and regulatory system across sites based on best practices
- Interface with internal and external customers, advocating for product quality
- Streamline quality processes and ensure alignment with global standards
- Analyze site assessment and audit trends, develop best practices
- Lead and develop direct reports, manage large workflows and multiple projects