Investigate, plan, and implement medical product improvements and evaluate critical quality monitoring processes directly affecting patient safety and product quality. Reduce defects of clients' devices, create quality products neatly. Writing and executing physical and chemical test method protocols. Use quality policies like EU MDR, 21CFR820 set forth by FDA, reply to customer complaints, perform audits, develop test methods, validation, etc. Travel in the context of role may be required at least 1-2 times per year based on clients' needs.
Apply with 2 copies of resume to HR ValidIT Solutions LLC, 8737 Dunwoody Pl Unit 4, Atlanta, GA 30350
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