The QA/RA Associate shall provide support for the development of innovative medical devices, as part of the COVARTIM QA/RA team. (S)he will provide support in Quality Assurance and Regulatory Affairs activities such as, but not limited to:

- Quality Management System implementation at our clients’ site
- Standards watch and gap analysis
- Audits
- Compilation of documentation for notified bodies, FDA, competent
authorities

Background:
Min. 2 years of relevant experience in medical devices QA/RA functions

Hard skills:
- Good understanding of medical devices regulatory environment (MDD 93/42, MDR)
- Good knowledge of medical devices quality assurance (ISO 13485) and relevant standards
- English and French/Dutch

More details on our website!

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