Consultant Medical Devices Regulatory - Brussels, België - Qserve Group B.V.
4 dagen geleden
Beschrijving
What you'll do**Qserve has an exciting opportunity to join our team as a Consultant Medical Devices Regulatory / US Submission Expert. As a consultant at Qserve, you serve a wide variety of clients in the medical device industry. With your regulatory knowledge of medical devices, you will be responsible for helping Qserve clients with regulatory writing, achieving FDA approval and getting US market access for a wide range of medical device products. You will be part of a team of medical device experts, working from all over the world, dedicated to supporting our clients.
What you'll bring to the team
- Technical or scientific degree (BSc, MSc, or PhD) in physics, mechanical engineering, chemistry, (medical) biology, biomedical technology, or similar;
- At least 5 years of working experience in regulatory and/or the medical devices field;
- Knowledge of US medical device regulations;
- Experience with writing technical documentation and regulatory documents for US submissions;
- Experience with Medical Device Quality management systems 21CFR820/ ISO 13485;
- Communicative and serviceoriented;
- Fluent in English.
Interested?
Getting excited about a career as a consultant in the dynamic and innovating world of medical devices? Then please submit
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