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LabWare LIMS Specialist

Katalyst Healthcares & Life Sciences

  • Thousand Oaks, CA
  • 1 day ago

    Highlights

    Support validation activities by providing clear documentation and traceability for configured LabWare objects following Takeda internal procedures. Support a dedicated workstream supporting implementation of raw material and commercial product processes within LabWare LIMS 8.

    Numbers & Facts

    LocationThousand Oaks, CA

    Description

    Key Responsibilities:
    • Workstream Leadership & Scope Definition
    • Support a dedicated workstream supporting implementation of raw material and commercial product processes within LabWare LIMS 8.
    • Define and manage LabWare build across:
    • Raw materials and commercial product master data
    Test workflows:
    • Laboratory equipment and interfaces
    • LabWare LIMS Configuration
    • Configure raw materials, commercial products including stability, and laboratory equipment in LabWare LIMS using standardized, compliant design patterns.
    Ensure LabWare configuration aligns with:
    • Approved test methodologies
    • Apply controlled build practices and normalized templates to ensure consistency, scalability, and compliance.
    Requirements Traceability & Validation Support:
    • Translate regulatory, quality, and operational requirements into standardized LabWare LIMS designs.
    • Support validation activities by providing clear documentation and traceability for configured LabWare objects following Takeda internal procedures.
    Instrument & System Integration:
    • Configure and support instrument interfaces between LabWare 8 and a variety of laboratory systems.
    • May develop or support parsing scripts, where required and permitted by Takeda standards and governance.
    • Support connectivity and data flow between LabWare and other GMP systems, such as LabX
    Operational Readiness & Execution:
    • Support stable execution of raw material and equipment workflows in live operations.
    • Troubleshoot configuration and integration issues impacting laboratory execution.
    • Partner with site teams to ensure LabWare configurations are fit for intended use and operationally sustainable.
    Must Haves:
    • Proven hands-on experience configuring LabWare LIMS (LabWare 8 strongly preferred).
    • Strong experience with Labware within GMP laboratory operations, particularly:
    • Raw materials testing
    • Commercial product testing
    • Laboratory equipment workflows
    • Demonstrated ability to translate regulatory and quality requirements into compliant LIMS configurations.

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