Quality Assurance/Document Control Specialist
Responsible for multiple administrative duties within the Quality System of a Medical Device company including document control, records management, and serve as the Training Coordinator for Documents. Additional duties include maintaining compliant supplier records, archive and store quality records, and conduct internal audits. This position is responsible for ensuring that all records created and maintained by the company are in compliance with FDA, ISO, QSR, quality, safety and environmental regulations.
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CLOSING DATE: FRIDAY 12th April at 6:00pm