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    Night Shift Process Technician - Huntsville, AL, United States - Integrated Resources, Inc

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    Description

    Job Title:
    Quality Control


    Job Location:
    Memphis, TN
    Job Duration : 8 Months+

    Shift:
    Sun. - Wed.

    7:30 AM – 5:30 PM or Wed. – Sat.

    7:30 AM – 5:30 PM
    (10-hour days with potential overtime)


    Job Description:

    The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material testing.

    The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation.

    In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success.


    Responsibilities:

    • Performs environmental monitoring, including air viable particulate, non-viable particulate and surface sampling and personnel monitoring.
    • Receives raw materials and supplies for the QC laboratory and maintains laboratory supplies, media and reagents inventory.
    • Adheres to standard operating procedures and good documentation practices to ensure data integrity and traceability.
    • Participates with maintaining proper overall operation of department (physical inventories, logs, documentation, filing, etc.)
    • Responsible for assisting with routine laboratory upkeep and organization.
    • Utilizes GMP systems such as MODA and other laboratory computer systems.
    • Reviews test results of other QC analysts for accuracy and precision and maintains and efficient workflow of all required testing documentation ensuring timely submission relative to product release dates.
    • Perform all other related duties as assigned.
    Required Education &

    Professional Experience:

    • Bachelor's degree in biology or relevant scientific discipline preferred.
    • Highschool diploma or equivalent required.
    • Minimum 0-2 years relevant laboratory experience or experience in a cGMP and/or FDA regulated industry, or a combination of education and related work experience required.
    • May consider less education and professional experience upon successful completion of Charles River's internship program.
    • Ability to work in Clean Room environment with full gowning requirements.
    • Ability to work independently or as a team member.
    • Detail-oriented with strong written and verbal communication skills.

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