Center Quality Specialist

rEVO Biologics, Inc.

  • Fort Pierce, FL
  • 8 days ago

    Highlights

    In the absence of the Manager of Center Quality Assurance: Conduct root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Ability to interpret a wide variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.

    Numbers & Facts

    LocationFort Pierce, FL

    Description

    Essential Job Responsibilities and Duties

    • Perform donor record file review
    • Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual
    • Review medical reports and communication
    • Perform reviews of equipment incidents
    • Verification and release of sample shipment
    • Responsible for the inspection and release of incoming supplies
    • Initiate deviation reports as needed
    • Perform Weekly employee observations
    • Assist the Manager of Quality Assurance with compliance of all state and federal regulations, FDA-approved Standard Operating Procedure Manual, Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP), Occupational Safety and Health Administration (OSHA), and internal company procedures
    • Reviews the documentation of unsuitable test results and the disposition of the associated units

    In the absence of the Manager of Center Quality Assurance:

    • Conduct root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product
    • Review of equipment records and donor system information, if applicable, to approve out of service equipment for use
    • Review and approval of deferred donor reinstatement activities
    • Review lookback information
    • Waste shipment review
    • Initiates investigations and reports any supplies that have not met quality specifications and requirements before use
    • Review medical incident reports and documentation

    Qualifications

    • High school diploma, GED or equivalent required. Associates degree preferred or a minimum of (3) three to (6) six months quality or plasma industry experience required.

    Requirements

    • Strong verbal and written communication skills
    • Must have above average problem-solving and decision-making abilities
    • Proficiency with computers
    • Must have explicit attention to detail
    • Must have excellent analytical skills, organization skills, and follow-up
    • Ability to read and interpret documents such as safety rules, operating and maintenance instruction, and procedure and technical manuals
    • Ability to interpret a wide variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables

    Physical Requirements

    • Use hands to handle or feel objects, tools, or controls; reach with hands and arms; and talk or hear
    • Frequent leaning, bending, stooping, crouching, and reaching above the shoulders and below the knee
    • Manual dexterity to perform all phases of donor plasmapheresis
    • Ability to make and analyze a physical assessment of heart, lung sounds, signs of drug use, etc.
    • Ability to stand for extended periods of time for up to four (4) hours at a time
    • Ability to lift, tug, pull up to fifty (50) pounds

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