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    Quality Control Research Associate - Santa Monica, United States - Planet Pharma

    Default job background
    Pharmaceutical / Bio-tech
    Description
    • Conduct non-routine analysis of raw materials, intermediates, and finished product samples.
    • Troubleshoot instrumentation and test methods.
    • Assists in the training of QC staff as needed.
    • Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices (GLP)
    • Working knowledge and proficiency with Microsoft Office software.
    • Evaluates equipment for purchase and performs installations and qualifications of the new instruments.
    • Writes and executes protocols, reports, and SOPs.

    MOST IMPORTANT PART: Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. Perform reviews of assays and maintain laboratory in a state of compliance.


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