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    validation Engineer(Medical Devices) - Irvine, United States - Pacer Staffing

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    Description

    Job Title:
    validation Engineer (Medical Devices)

    Duration: 09Months


    Location:
    Irvine, CA

    Summary


    The main function of a is to apply engineering theory and principles to problems of industrial layout or manufacturing production.

    A typical manufacturing engineer has the ability to make engineering drawings and read and interpret blueprints.

    Essential Responsibilities And Duties


    Required to transfer equipment from PR site to IRV, install and qualify the equipment, commission the cleanroom, write validation protocols/reports, execute validation activities (IQs, TMVs, SWV, TFIQs, OQ/PQ, CQ), draft procedures, drawings, process sheets, planning/procurement of raw materials needed, and anything else necessary.


    Support the needs of the mfg line – equipment troubleshooting, document review, own NCRs and CAPAs as necessary, support equipment maintenance, planning/scheduling, raw material/supply procurement, support Supplier Quality Engineering activities, training of operators, act as SME for technical purposes, change management (procedures/drawings, etc.), support internal/external audits, etc.

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