Post-Market Surveillance & Vigilance Specialist
- 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.
- 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.
Post-Market Surveillance & Vigilance Specialist
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