Description

Entreprise :

Our client is an international company specialized in medical devices.

Description du poste :

* Vigilance & complaint processes management ;
* Support in post-market surveillance activities ;
* Medical device data management, creation and maintenance of associated documentation ;
* Support in QMS improvements and audits ;
* Ensure regulatory compliance and process optimization ;
* Cross-functional collaboration and advice to internal teams.

Description du profil :

* Academic background in engineering;
* Minimum 3 years of experience within a medical devices company ;
* Experience with vigilance, post-market surveillance and complaint management is required ;
* Knowledge of medical devices regulations (EU-MDR, ISO 13 485...) ;
* Audit experience is a plus ;
* Proficiency in French and English is mandatory.