Overview

Job Description Job Description LabWare LIMS Configuration & Integration Specialist (LabWare 8) - Local Only - W2 - BB10108 this role will focus on validation document generation for the above and liaison with onsite SMEs.BB10108Newberry Park, CA (Thousands Oak)9+ MonthsHybrid - Must be local - W2 OnlyJob SummaryLabWare LIMS Configuration Specialist to support the LabWare 8 upgrade for a US based GMP laboratory site. This role will lead a dedicated workstream focused on implementing raw material and commercial product workflows, completing master data configuration, and finalizing integration with laboratory equipment and enterprise GMP systems.The successful candidate will translate regulatory, quality, and operational requirements into standardized, compliant LabWare LIMS designs and ensure stable execution of configured workflows in a regulated manufacturing environment.Key ResponsibilitiesWorkstream Leadership & Scope DefinitionSupport 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 dataTest workflowsLaboratory equipment and interfacesLabWare LIMS ConfigurationConfigure raw materials, commercial products including stability, and laboratory equipment in LabWare LIMS using standardized, compliant design patterns.Ensure LabWare configuration aligns with:Approved test methodologiesProduct specificationsSampling plansApply controlled build practices and normalized templates to ensure consistency, scalability, and compliance.Requirements Traceability & Validation SupportTranslate regulatory, quality, and operational requirements into standardized LabWare LIMS designs.Support validation activities by providing clear documentation and traceability for configured LabWare objects following Client internal procedures.Instrument & System IntegrationConfigure and support instrument interfaces between LabWare 8 and a variety of laboratory systems.May develop or support parsing scripts, where required and permitted by Client standards and governance.Support connectivity and data flow between LabWare and other GMP systems, such as LabXOperational Readiness & ExecutionSupport 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.Required QualificationsProven hands on experience configuring LabWare LIMS (LabWare 8 strongly preferred).Strong experience with Labware within GMP laboratory operations, particularly:Raw materials testingCommercial product testingLaboratory equipment workflowsDemonstrated ability to translate regulatory and quality requirements into compliant LIMS configurations.Experience supporting LIMS validation with full requirements traceability.Experience integrating LabWare with:Instrument systems (e.g., Empower, LabX)Strong cross functional communication skills in regulated environments.Preferred QualificationsExperience supporting LabWare upgrades or major LIMS implementations.Experience working in biopharmaceutical or pharmaceutical GMP environments.Experience supporting inspection readiness activities related to LIMS.Deliverables & Success CriteriaCompleted on time LabWare LIMS configurations for raw materials, commercial products, and equipment integration.Clear requirements to configuration to validation traceability.Stable, compliant execution of configured workflows in operations.Successful integration between LabWare and laboratory instrumentsAdditional NotesThis role requires close collaboration with Client Quality, Validation, IT, and Laboratory teams.Work must follow Client change control, validation, and data integrity requirements.Onsite presence may be required based on project phase and site needs.TechData is proud to be an equal opportunity wo