Excellent opportunity with medical device manufacturrer in Clearwater, FL. Assist in the design and implementation of policies and procedures to insure quality standards are met during production, that company products meet customer expectations and achieve superior reliability while maintaining compliance with Federal, State and other regulations and standards governing the medical device industry, including but not limited to FDA, ISO, UL, OSHA, EPA, ASTM, ANSI. Snapshot of Duties (not all inclusive): Assist with the management and submission of recalls/FSN’s and adverse event reports. Prepare monthly quality trending reports. Coordinate and process nonconformance reports - e.g., log, investigate. Coordinate re-wor
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