Vigilance Specialist

A globally recognized manufacturer in the medical device industry is looking to strengthen its Post‑Market Surveillance & Vigilance function. The company develops advanced technologies used across intensive care, emergency transport, and other critical healthcare environments, supporting a wide range of clinical applications.

How you will contribute:

• Conduct reportability assessments for incoming post‑market events
• Prepare initial vigilance reports within required timelines
• Take responsibility for meeting deadlines and complying with regulatory timeframes
• Create final reports based on completed investigations
• Communicate effectively with internal teams and external partners
• Manage communication with health authorities, including cases of higher complexity
• Prepare overviews and summaries of reported events for regulatory bodies
• Generate statistics for the annual management review