Regulatory Affairs Specialist — Junior
As a RA Specialist, you will support the QA&RA; team in ensuring that our medical devices comply with international regulations. You will support the preparation and update of technical documentation, the submissions to Notified Bodies and Competent Authorities, and stay ahead of the evolving regulatory landscape in the EU (MDR) and US (FDA).
Key Responsibilities
- Regulatory Intelligence: Monitor changes in international regulations (e.G. MDR), standards (e.G. ISO, ASTM), and guidance
Key Responsibilities
- Regulatory Intelligence: Monitor changes in international regulations (e.G. MDR), standards (e.G. ISO, ASTM), and guidance