5-7 years of hands-on experience configuring LabWare LIMS, preferably LabWare 8.
Strong background in GMP laboratory operations, especially in raw materials and commercial product testing.
Experience with laboratory equipment workflows and integration.
Ability to translate regulatory and quality requirements into compliant LIMS configurations.
Familiarity with validation activities and documentation standards.
Responsibilities
Lead workstream and define project scope for LabWare LIMS implementation.
Support the implementation of raw material and commercial product processes within LabWare LIMS 8.
Manage LabWare build for raw materials and commercial product master data.
Configure laboratory equipment and interfaces in LabWare LIMS.
Ensure LabWare configuration aligns with approved test methodologies and controlled build practices.
Translate regulatory and operational requirements into standardized LabWare designs.
Troubleshoot configuration and integration issues impacting laboratory workflows.
Benefits
Opportunity to work with cutting-edge laboratory information management systems.
Collaborative environment with site teams to ensure operational sustainability.
Engagement in compliance-driven projects that enhance laboratory efficiency.
Potential for professional growth within a leading pharmaceutical company.
Full Job 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 dat
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:
pproved test methodologies
pply 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.
