Job Title – Sr Quality Engineer – Medical Device
Job Location – 1480 Arthur Ave, Unit D, Louisville, Colorado, United States of America, 80027
Duration – 06 Months
Technical Skills Must Have:
3+ years of experience in the medical device industry, with a strong background in Non -Conforming Materials Reports (NCMR), CAPA, or product quality management. Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, EU MDR, and other relevant medical device regulations. Proven experience leading NCMR and CAPA processes, ideally within a medical device or regulated industry. Strong project management skills, with the ability to manage multiple…
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