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Quality/Regulatory Director |
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Summary: or email this job to apply later Serves as the official correspondent to FDA, responsible for the annual registrations and device listings. Ensuring compliance with FDA and other applicable international regulations and requirements for the design and development of medical devices and provide general regulatory support to the organization. Responsible for leading all RA related activities Facilitate external Quality System audits (ISO registration, Client Supplier Quality, etc.) and guide the organization during FDA Inspections (QSIT format). The position will be responsible for ... | |
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