To thrive and succeed in this role, we believe that you bring the following experiences:
- Relevant academic education.
- A few years of work experience in QA within Med Tech or pharmaceuticals.
- Competence within Risk Management according to ISO14971 or within RA.
- Fluent in English, both spoken and written.
If you have experience with MDR for medical device class II or III products and have worked with medical technical products made of plastic, it will be considered advantageous. Additionally, competencies in the standard series 60601, risk management according to ISO14971 and RA, and knowledge of QSReg will be highly regarded. Fluency in Swedish is also an advantage for this role.
Triomed is seeking a candidate who is able to work both independently and in close collaboration with others. The ideal candidate has an eye for detail without losing sight of the big picture. They should be confident and thrive in a dynamic environment.