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    Operations Quality Engineer - Austin, United States - Katalyst Healthcares and Life Sciences

    Katalyst Healthcares and Life Sciences
    Katalyst Healthcares and Life Sciences Austin, United States

    2 weeks ago

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    Description


    Operations Quality Engineer To support our extraordinary teams who build great products and contribute to our growth, we're looking to add an Operations Quality Engineer located in Austin, TX.


    What a typical day looks like:
    Develops and initiates standards and methods for inspection, testing and evaluation. Devises sampling procedures and designs and develops forms and instructions for recording, evaluating and reporting quality and reliability data. Develops and implements methods and procedures for disposition of discrepant material and devises methods to assess cost and responsibility. Directs workers engaged in measuring and testing product and tabulating data concerning materials, product or process quality and reliability. Compiles and writes training material and conducts training sessions on quality control activities. Supports Product Engineers and Quality Program Managers with customer interfaces as necessary on quality related issues. Assures data availability and integrity for all quality related data. Consolidates and reports quality results. Initiates corrective action requests as needed and tracks to satisfactory completion. Assists with development and implementation of quality audits.

    Responsible for developing, applying, revising and maintaining quality standards for processing materials into partially finished or finished products Designs and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and/or production equipment.

    Analyzes reports and returned products and recommends corrective action.

    Approves product, process and equipment qualifications Provides liaison to various regulatory bodies The experience we're looking to add to our team: 5 years of quality engineering experience in Medical Device regulated environment Bachelor's degree in engineering or equivalent experience Manufacturing experience NCMR (non conformance material report) experience
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