Post-Market Surveillance & Vigilance SpecialistMichael Page

Our client is an international company specialized in medical devices.

• 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.