- Manage a portfolio of assigned projects and provide functional expertise in area of responsibility for medical devices and combination products
- Provide Quality and Regulatory guidance in development projects of combination devices
- Write, review and approve deliverables (e.g. procedures, records, third party work, clinical trial material, components) to ensure GMP compliance
- Support Medical Device Risk Management, through proactive risk management tools and approaches, to minimize the impact on global supplies and patients - Release of medical devices for clinical studies and commercial use
- Perform inspections and audits