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    Technician, Quality - Metuchen, United States - Cole-Parmer

    Cole-Parmer
    Cole-Parmer Metuchen, United States

    3 weeks ago

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    Description
    Job Description


    Job Title:
    Technician, Quality


    Reports To:
    Supervisor, Quality


    Position Location:
    Metuchen, NJ


    FLSA Status:
    FLSA Status : Non-Exempt


    Position Summary:


    Responsible for quality system processes designed to ensure continuous flow of incoming and outgoing materials consistent with established standards and regulations including ISO9001, FDA 21 CFR 820, ISO 13485, and appropriate EU regulations .

    Ensures compliance in Quality areas including review and generation of information for incoming materials and product release. Ensures compliance in the areas of equipment qualification and calibration, supplier qualification and management, and document control as needed.

    Ensures continued improvement and compliance with relevant regulations by participating in audit responses, and deviation, nonconformance, complaint, and CAPA processes as necessary.

    Promotes and participate in training activities related to the quality management system and product quality, safety and efficacy.


    Key Responsibilities:


    Where required, responsible for performing final quality checks on all outgoing product shipments, which includes reviewing and assuring accuracy of both documentation and product in a lab setting.

    Responsible for release of incoming materials, manufactured materials, and finished products according to written specifications.

    Assist with the maintenance of the equipment qualification and calibration program and upkeep of the equipment database.


    Assist the Quality Manager with review and filing of calibration certificates, out of tolerance reports, deviations, and SCARs as necessary.

    Assist with the development and implementation of company SOPs as assigned.

    Perform document control and training activities as assigned.


    Requires an ability to complete cGMP / product documentation accurately, in accordance with standard operating procedures, and in a timely manner.

    Requires an ability to work independently to accomplish given tasks within given timelines.

    Requires an ability to multitask and adjust to changing priorities.

    Must report any deviations or nonconformities immediately to a supervisor or above.

    Other duties as assigned.


    Education:
    Associates Degree or above in related field or equivalent work experience is required.


    Experience:
    1 or more years of previous related experience

    MS Office Suite proficiency.


    Minimum Requirements/Qualifications:
    Good communication and organizational skills and ability to multitask.

    Prior experience with ISO9001 or ISO 13485 and 21 CFR 820 a plus.

    Thrives in a fast-paced, collaborative environment, efficiently works under pressure, within deadlines or other time essential constraints

    Excellent communication skills, both written and verbal, to clearly and concisely communicate to all levels of the organization

    Strong work ethic and an ability to excel within a rapidly changing and growing organization


    Physical Requirements/Working Conditions:
    Control exposures to hazardous chemicals & other safety hazards such as:

    Carcinogens.

    Strong and obnoxious fumes.

    Sharp and dangerous blades and needles.

    Biohazard exposure to specimens.

    This position has not been approved for Relocation Assistance.


    The above statements are intended to describe the general nature and level of the work being performed by people assigned to this job.

    They are not an exhaustive list of all of the duties and responsibilities associated with it.


    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.

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