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    Senior Quality Control Associate - Irvine, United States - EPM Scientific

    Default job background
    Pharmaceutical / Bio-tech
    Description

    Senior Quality Control Chemist

    5-days on-site in Irvine, CA

    A small, well-established CDMO in Irvine, CA, wants to add a QC Chemist to their team. Join this team to expand on your analytical experience in a cGMP environment. The organization supports its employees' growth and development, helping employees succeed in the pharmaceutical industry while supporting their network of clients.

    Currently, the team is only considering candidates local to Irvine, CA, or candidates with a sustainable commute to their labs.

    RESPONSIBILITIES:

    • Run analytical test methods for raw materials, in-process samples, and finished products
    • Peer review data from chemists
    • Write, perform, and validate analytical methods/SOPs, and maintain analytical instrumentation
    • Support method transfers and equipment calibrations
    • Support with training other lab-based employees
    • Provide support for internal and customer audits

    QUALIFICATIONS:

    • Bachelor's degree in chemistry or related discipline.
    • 8+ years' experience with analytical instrumentation
    • 8+ years of experience in Chemistry Lab
    • 5+ years' experience in GMP/GLP environment.


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