Global Product Monitoring Vigilance Report Writer
About this role
Global Product Monitoring Vigilance Report Writer
Job Summary
We are seeking an experienced Medical Device Vigilance Specialist with deep expertise in French vigilance requirements and direct experience working with French Competent Authorities.
This position is focused on ensuring compliance with French post-market surveillance and vigilance obligations. Unlike broader international roles, this opportunity is ideal for someone who has built significant expertise navigating the French regulatory environment and wants to be recognised as a subject matter expert.
What You'll Do
- Lead French vigilance reporting activities and ensure compliance with applicable regulations.
- Serve as a key point of contact for interactions involving French Competent Authorities.
- Review adverse events, complaints and field issues to determine reportability requirements.
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