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  • Quality Engineer

    Accellent - Trenton, GA

    regulations and standards such as (where applicable) US21 CFR Part820 (FDA QSR, cGMP) ISO 13485 (EN) ISO 13485 Medical Devices Quality Management Systems EU Medical Device Directive (MDD) 93/42/EEC EU Active Implantable Medical Device...

    30+ days ago from Accellent Inc.

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