Regulatory compliance (Medical devices) - Intern
vCare Denmark is developing telemedicine software to help chronic patients get best possible care and quality of life using patient engagement, motivation and empowerment.
We aim to improve care and disease management, and reduce hospitalisation rates for high-risk patients. The ambition is to increase access to healthcare for patients who face barriers such as distance, transportation, or caretaker availability giving equal access to healthcare services for all. We aim to be compliant with regulatory requirements for our product but at the same time offer help to other customers in relation to regulatory compliance. We have experience with class 1 and 2 medical devices (MDR) and would like to strengthen our team.
You must have technical knowledge and understanding of MDR and ISO standards associated with it. You must have good sense and high respect for quality assurance. We at vCare Denmark would be able to connect your knowledge to application and practice. For more information or questions please contact us at kv@vcareit.dk or phone number 41882399.
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