About this opportunity
Cordis lists this Medical Device Quality & Regulatory Specialist II opportunity in town of florida, New York. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Cordis is seeking a Product Complaint Analyst in New York to review, evaluate, classify and follow up on product complaints for medical devices, ensuring compliance with FDA MDR/MDV and other regulations. The role requires independent work on complex issues and close collaboration with management.
You will support audits, document procedures, and participate in regulatory reporting while maintaining high standards of quality and patient safety.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.