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    TekWissen llc

    Software Engineering

    Quality Engineer- Medical Device Manufacturing

    Miami, United StatesOn-SiteContract3+ yrs experiencePosted 3w ago
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    Job description

    • Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers.
    • Develops and implements corrective/preventative action plans.
    • Collects and analyzes data for gauge and product evaluation.
    • Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.
    • Ensures that suppliers have necessary information and facilities to deliver quality products
    • Ability to deliver, meet deadlines and have results orientation.
    • Able to communicate both orally and in written form to multiple levels of the company.
    • Demonstrates characteristics of high potential for future development opportunities.
    • Microsoft Office Suite
    • Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs.

    B.S. in engineering or an alternative Bachelor’s degree program with certification as a quality engineer (e.g. CQE) plus 3 years experience in a Quality Engineering role, or an equivalent combination of education and experience. Certified Quality Engineer (CQE) preferred.

    Job details are sourced from the employer's original posting.

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    About the company

    TekWissen llc

    TekWissen provides a unique portfolio of innovative capabilities that seamlessly combines clients insights, strategy, design, software engineering, and systems integration.

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    Industry
    Software Engineering
    Open roles
    169

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