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    Quality Engineer - Temecula, United States - GForce Life Sciences

    GForce Life Sciences background
    Description

    Responsibilities:

    • Consult with Manufacturing, Information Management, Research Development & Engineering, Quality Assurance Operations, and Product Performance Analysis teams to ensure compliance with LifeScan software development procedures and industry regulations
    • Review and approve deliverables of the software development lifecycle
    • Lead teams in performing Hazard Analysis
    • Occasionally assist teams in developing Standard Operating Procedures and Work Instructions for software development activities tailored to their specific needs
    • Occasionally provide training for select software development activities for LifeScan
    • Occasionally write and execute test protocols and reports

    Requirements:

    • Bachelor's degree in Engineering required, Mechanical Engineering or Biomedical degree is a plus
    • Minimum of 3-5 years of experience required
    • Attention to detail and proficiency in managing reports and regulatory compliance

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