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    Specialist, Quality Assurance/Compliance/Safety - Irving, United States - Quest Diagnostics Incorporated

    Quest Diagnostics Incorporated
    Quest Diagnostics Incorporated Irving, United States

    3 weeks ago

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    Description
    Our goal is to provide every patient and every customer with services and products of superior quality. We do that through commitment, leadership, and establishing rigorous processes which we measure and continually improve upon.


    The QA Specialist position is intended to provide oversight and support for the Quality Program-Quality Management Planning, inspection preparedness and responses associated with laboratory accreditation, non-conformance management and Document Control management, and training and competency monitoring.

    Work with the Laboratory Director and Department Supervisors to facilitate the Quality Management Planning process.


    • Identify and monitor quality indicators.
    • Schedule and conduct Quality Meetings and distribute the minutes.
    Ensure inspection preparedness by conducting internal audits of laboratory processes to identify non-conformances and areas of needed improvement.


    • Appropriate Authorization, Delegations, and associated Performance Assessments
    • Training and Competency documented via MediaLab.
    • Testing Exceptions
    Effectively create and complete Corrective and Preventive Actions (CAPAs) for areas where non-conformances are identified.


    • Immediate Corrective Actions
    • Preventative Actions with Patient Remediation
    • Continuous monitoring and Effectiveness Checks
    License Coordinator for accreditation licensure.

    Quality metrics data collection and analysis to identify trends and needed interventions.

    QA Record organization and adherence to record retention requirements.


    Responsible for management of the CAP website as applicable for the organizational profile as well as testing and supervisory personnel.

    SmartSolve Software Administration for Document Control.


    • Manage SOP Life Cycle (Implementations, Recurring Reviews, Administrator monitoring reports).
    Other duties as assigned.


    Education:

    • Bachelor's Degree (Medical Technology or Chemical, Biological, or Clinical Laboratory Science) preferred.

    Work Experience, Technical Training, or Professional Licensing:

    • At least three years' experience and associated knowledge of Laboratory regulations (CMS/CAP/NYS) and accreditation processes in a Medical Laboratory-Clinical or Anatomic Pathology.
    • Lean Six Sigma (Continuous Improvement) experience preferred

    Other:

    • PC application skills in Microsoft Office including Excel and Access.
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