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Millennium Software and Staffing Inc. is seeking a Quality Engineer to support regulated medical device development on site in Massachusetts. This mid-senior level contract role focuses on quality assurance practices in line with 21 CFR 820, ISO 13485, ISO 14971, IEC 62304, DHF/DMR/DHR documentation.
The position targets onsite work in multiple MA locations with a strong emphasis on compliance, risk management, and cross-functional collaboration in medical equipment manufacturing environments.
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Looking for Quality Engineering supporting regulated medical device development
standards and regulations (e.g., 21 CFR 820, ISO 13485, ISO 14971, IEC 62304
DHF, DMR, and DHR
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