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    Quality Engineer - Houston, United States - United Imaging North America

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    Description
    Job Description


    Job Description Description:
    Who are we?

    UIH is a leading global medical device developer and supplier with a diversified portfolio of advanced imaging equipment and healthcare IT solutions.

    We are building an innovative team with the mission of developing and supplying advanced technologies and improving patient care worldwide.

    As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


    Company Page:


    Responsibilities
    Establishes Quality procedures and work instruction for Quality inspection and related areas. Trains personnel in these documentation and other technical process controls
    Ensures control plans and associated documentation are implemented effectively and maintained
    Drive Non-conformance processes; Quarantines, documents and evaluates products and materials; follow up with the action items and ensure they are closed out in a timely manner
    Manage Engineering Changes orders and engineering change process
    Support internal, external audit, management review, and quality data reporting
    Manage the calibration of tools and oversee equipment maintenance activities
    Plans, implements, and oversees the daily operations of EHS and Radiation Safety
    Oversees the review of radiation human-use clinical research protocols
    Provide training and/or other education as necessary to ensure the health and safety of employees and comply with safety regulations
    Manages the personnel dosimetry program
    Inspects organizational facilities (safety audits) to detect existing or potential incident and health hazards, determines corrective or preventative measures where indicated, and follow up to ensure measures have been implemented

    Requirements:
    Bachelor degree or above in engineering or science;
    2 years QE experience in medical device, automobile or other mechanical and electrical industries or experience in other field of quality management (preferred);
    Experience in project management (preferred)
    Be able to work in magnetic environment (e

    g:
    no implantable metal in body)
    Familiar with ISO13485 (preferred)
    Familiar with FDA medical device regulation
    Skills
    Excellent communication (written and oral) and ability to create and deliver presentations/ trainings.
    Excellent ability to multitask, attention to detail, and organizational skills
    Strong analytical skills
    Team player
    Work proactively;

    #J-18808-Ljbffr


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