Supplier Quality Liaison / Engineer

Medical Device Quality Assurance Specialist

This is an onsite position. The purpose of this position is to initiate medical device quality assurance activities. These activities must be in accordance with FDA Quality System Regulation, ISO13485 and other international standards. This position will also support device complaint investigation and failure analysis as required.

Essential Duties and Responsibilities :

• Initiate medical device quality assurance activities
• Ensure compliance with FDA Quality System Regulation, ISO13485, and other international standards
• Support device complaint investigation and failure analysis