Your mission
Your Mission: You will play a key supporting role in the development and upkeep of regulatory documentation to ensure compliance with global standards. Key tasks include:
- Support the creation, submission, and maintenance of regulatory documentation
- Liaise with Research & Development to create and maintain technical files
- Monitor regulatory requirements and help integrate them into product development
- Assist with literature reviews and preparation of clinical evaluation reports
- Contribute to the development and improvement of department procedures