Offer summary
Qualifications:
At least 4 years in healthcare products, 2 years in in-vitro diagnostic devices, Degree in relevant technical field, Proficient communication using electronic platforms, Strong written English skills.
Key responsabilities:
- Conduct technical file reviews for EU IVDR compliance
- Identify and rectify compliance issues in device technical files
- Support CE marking and develop training materials
- Communicate with team and stakeholders effectively
- Stay updated on technologies and regulations