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.