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    Manufacturing Technician/Associate - Los Angeles, United States - BioPhase

    BioPhase
    BioPhase Los Angeles, United States

    Found in: Appcast US C2 - 1 day ago

    Default job background
    Description

    The Manufacturing Technician/Associate is responosible for ensuring the onstime delivery of quality biopharmaceutical products and supporting cell culture manufacturing. This role reports directly to the Manufacturing Supervisor.

    **US Citizens or Greencard Holders only**

    Pay Rate: $25-35/hr

    Location: Los Angeles Metropolitan Area

    Responsibilities:

    • Perform all tasks associated with the manufacture of clinical product following batch records and SOPs
    • Cell culturing and aseptic techniques
    • Work as part of a small team to execute GMP runs in close collaboration with Process Development, Facilities and Quality departments
    • Assist in the development of standard operating procedures (SOPs), master batch records (MBRs), deviations and change controls
    • Ensure right-the-first time performance of all process steps specific to the phase or state of operation, as well as drive the safety-first culture
    • Assist with authoring new or revise existing SOPs, MBRs, and other process documents
    • Successfully troubleshoot processing and equipment issues
    • Daily, real-time review of in-process cGMP documentation for completeness and accuracy
    • Assist with change control and investigations required to manage deviations
    • Train personnel on applicable procedures and equipment.
    • Other duties as assigned

    Qualifications:

    • Bachelor's degree required in a life science field such as biology, biotechnology, or chemical engineering; Associate's degree for the Technician level
    • At least two years of relevant life sciences industry experience; 0-1 years for the Technician level
    • Cell therapy-based therapeutics or other cell-based products is a plus
    • Strict adherence to SOPs and cGMP regulations, the ability to accurately complete documentation associated with clinical manufacturing
    • Excellent aseptic/sterile techniques and prior experience with cell culture, cell culture equipment
    • Must be able to work under aseptic conditions in a class 100 environment
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