Cary, Illinois
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Today
Description Thorough knowledge and understanding of US and International Medical Device Regulations, including MDSAP, with direct experience in US 510(k) and EU Class II devices. Strong knowledge of Quality Systems (Measurement, Analysis, and Improvement; Adverse Event and Advisory Reporting; Purchasing; Design and Development; Production and Service Controls, etc.) Expert working knowledge of regulatory requirements, standards, and regulations with significant audit experience. Strong communica
Easy Apply
Contract
USD 80.00 - 85.00 per hour