Adverse Event Reporting Spec II, Temporary (6 months)

This role supports the Post Market Surveillance and Vigilance group in managing Medical Device Reporting (MDR) to global health authorities like the FDA and Health Canada. Key duties include reviewing complaints for regulatory compliance, coordinating information requests, maintaining adverse event files, and assisting with regulatory audits. The position involves collaborating with engineering and quality teams to ensure timely and accurate submissions while implementing corrective actions to improve quality systems.