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    Quality Engineer - New York, United States - Kelly Science, Engineering, Technology & Telecom

    Kelly Science, Engineering, Technology & Telecom background
    Description
    Kelly Science, Engineering, Technology and Telecom

    a managed solution provider and business unit of Kelly Services, is currently seeking

    Design Quality Engineers

    for a long-term engagement at one of our

    Global Medical Device Manufacturing

    clients located in

    Santa Clara, CA .

    This role is a full-time, fully benefited position.

    As a Kelly SETT employee you will be eligible for 50% paid Medical & Dental, 401K and a variety of other benefits to choose from.

    You will also be eligible for paid time off, including holiday, vacation, and sick/personal time. All Kelly employees in this group receive annual performance reviews.

    Robotics & Digital Solutions


    client is a global leader in surgery with products and solutions found in almost every operating room around the world.

    Our Client has made significant contributions to surgery for more than 100 years from creating the first sutures to revolutionizing surgery with minimally invasive procedures.

    Continuing dedication to Shaping the Future of Surgery is built on their commitment to help address the world's most pressing healthcare issues and improve and save more lives.

    Through their surgical technologies and solutions including robotics, digital solutions, sutures, staplers, energy devices, trocars and hemostats and their commitment to treating serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact.


    Responsibilities:
    Design Quality engineers
    Purpose - is to hire quality engineers to help support the sub-system quality engineering team
    Design verification protocols/reports, Summary report
    Support review of


    NPD
    verification protocols/reports, test method validation, test fixture design review/qualification
    Review regression analysis and ensure that impacts are clearly justified
    Support Installation qualification of non-product software, test equipment
    Support

    risk management

    activities specifically review of dFMEA for the sub-systems
    Support cross-functional collaboration on key quality processes such as defect tracking/resolution, test execution
    Support review

    of build protocol / build report, DHR and configuration change

    and its impact on Design Verification reports
    Review design changes including mechanical and electrical drawings
    Support creation and review of Inspection plan for components and sub-assemblies
    Support review of Design Control deliverables

    Requirements:
    Bachelor's degree preferred but Associate degree is acceptable
    Minimum of

    • 5 years of design quality engineering and NPD
    Experience in a

    medical device manufacturing environment
    GD&T knowledge (Preferred)
    Previous work experience engaging in a team-based environment
    Experience with

    medical electrical-mechanical systems
    Knowledge of

    FDA requirements for design control of medical devices.
    Understanding of

    Risk Management process per ISO

    For immediate consideration, please apply online. This position is recruited for by a remote Kelly office and not your local Kelly branch. No sponsorship is available at this time. (no OPT, C2C or H1B Visa)


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