Quality Control Analyst - Novato - GForce Life Sciences

    GForce Life Sciences
    GForce Life Sciences Novato

    1 day ago

    Pharmaceutical / Bio-tech
    Description

    QC Analyst

    12-month Contract

    Onsite in Novato, CA

    Must be able to work on a W2

    SUMMARY

    The QC Analytical Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.

    RESPONSIBILITIES


    • Performs, under minimal supervision, biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines. General cGMP lab experience at the Analyst level.


    • Works independently on assays they have mastered


    • Develops and maintains proficiency in a broad range of test methods


    • Develops a technical understanding of each assay and assists with trouble shooting and laboratory investigations


    • Evaluates data against defined criteria/specifications


    • Actively applies knowledge in non-routine situations using a thorough understanding of the work processes and practices


    • Identifies key issues in complex situations, analyzes problems, and makes sound decisions


    • Assists in the revision of written procedures, method/equipment validation, and/or method transfers as assigned


    • Mentors and trains other analysts, including new hires and more junior analysts, in areas of expertise


    • Holds self and others accountable for adherence to department and company policies and practices


    • Maintains a safety and quality focused culture

    EXPERIENCE


    • B.S./B.A. in Science (Major in Chemistry, Biology, Biochemistry).


    • 1-2 + years of experience in a cGMP/GLP laboratory


    • 1-2+ years hands-on experience in separation sciences (HPLC, UPLC, CE)


    • Ability to follow written instructions and to perform tasks with direct or minimal supervision


    • Strong leadership skills demonstrated through past work history


    • Use of a computer: e.g., Proficient in Windows, Microsoft Word, Excel


    • Good written and verbal communication skills


    • Attention to detail and strong documentation skills


    • Ability to contribute effectively in team environments and independently


    • 1-2+ years of Quality Control laboratory experience preferred


    • 1-2+ years of hands-on experience in separation sciences (HPLC, UPLC, CE) preferred


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