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    Quality Engineer - Scarborough, United States - GForce Life Sciences

    GForce Life Sciences
    GForce Life Sciences Scarborough, United States

    2 weeks ago

    GForce Life Sciences background
    Description

    Internal Title:
    Engineer, Quality

    Duration: 6-month

    Location:
    Onsite in Scarborough, ME

    Responsibilities
    production with resolution of quality issues in accordance with established procedures.
    production on the manufacturing floor, ensuring adherence to procedures and ensure appropriate device history record (DHR) documentation. Supports line clearances, reworks, and inspections as required.
    commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.

    for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices.

    and is aware of the quality consequences that may occur from the improper performance of their specific job.

    Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.

    duties as assigned, according to the changing needs of the business.

    Qualifications
    Bachelor's degree or equivalent in a related field
    Some previous quality experience
    Experience with batch records, SOPs, structured documentation
    Familiar with quality management systems (agile)

    #J-18808-Ljbffr

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