Summary
ECI in Marlborough, MA is seeking a specialist to investigate, document, and close out customer complaints regarding medical device performance. The role ensures adherence to FDA 21 CFR 820, ISO 13485, and MDR requirements, contributing to a compliant lifecycle process.The ideal candidate will collaborate with cross-functional teams to address non-conformities and drive quality improvements. This position offers exposure to life sciences regulatory frameworks and opportunities to influence#J-18808-Ljbffr
Job Description
ECI in Marlborough, MA is seeking a specialist to investigate, document, and close out customer complaints regarding medical device performance. The role ensures adherence to FDA 21 CFR 820, ISO 13485, and MDR requirements, contributing to a compliant lifecycle process.The ideal candidate will collaborate with cross-functional teams to address non-conformities and drive quality improvements. This position offers exposure to life sciences regulatory frameworks and opportunities to influence#J-18808-Ljbffr
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