path to what they both need - answers. Responsibilities The Quality Specialist-Post Market will support the growth... complaints to determine reportability in accordance with 21 CFR Part 803 Medical Device Reporting, European Vigilance Reporting...
experience with Quality Management Systems, Change Control, Audits, CAPA Your knowledgeable in ISO 13485:2016, CFR Part 820... solving. Your experience in change management What you’ll get: A front row seat to life changing CGM technology...
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