Functieomschrijving
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
Location
Boulevard du Souverain 36, 1170 Watermael-Boitsfort (Brussels)
Function type
Full time open-ended
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
Soft skills
- Passionate about life sciences, technology and innovation
- Quality and customer-service oriented
- Focused on details
- Strong communication and organizational skills
- Autonomous & quick learner
- Flexible & open-minded
Ons aanbod
The opportunity to contribute to the development of products that will improve or save people’s life
A valorizing job within an ambitious and growing company in a booming industry
A great team of enthusiastic people led by passionate experts in MedTech
A nice working environment in our new office located in Brussels, close to the forest of Soignes, a park, nice shops and restaurants, public transport connections and the E411
And of course, a good salary package and extra benefits!
Solliciteer
Get to know us better and apply on Welcome to the Jungle :Send your application letter and resume to
Kyun Thibaut
Managing Director
jobs@covartim.com
