LabWare LIMS Validation Specialist (Onsite role)

Job Title LabWare LIMS Validation Specialist (Onsite role) Contact Please let me know if you are interested or anyone who might be interested. Client Major Pharmaceutical Client Position Details Position: LabWare LIMS Validation Specialist (Onsite role) Duration: 9+ Months (Contract) Location: Newbury Park (Thousand Oaks), CA 91320 Pay Rate: $90.00 – $100.00 per hour Employment Type: W2 Description mary:LabWare LIMS Configuration Specialist to support a LabWare 8 upgrade for a 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 sys tems.The successful candidate will translate regulatory, quality, and operational requirements into standardized, compliant LabWare LIMS designs and ensure stable execution of configured LabWare objects following internal procedures in a regulated manufacturing environment. Key Responsibilities ties:Support a dedicated workstream supporting implementation of raw material and commercial product processes within LabWare Li MS 8.Define and manage LabWare build ac ross:Raw materials and commercial product master flowsLaboratory equipment and inter LabWare LIMS Configuration ationConfigure raw materials, commercial products including stability, and laboratory equipment in LabWare LIMS using standardized, compliant design patt erns.Ensure LabWare configuration aligns with:Approved test methodol ogiesProduct specifica tionsSampling plansApply controlled build practices and normalized templates to ensure consistency, scalability, and compli Traceability & Validation supportTranslate regulatory, quality, and operational requirements into standardized LabWare LIMS des igns.Support validation activities by providing clear documentation and traceability for configured LabWare objects following internal proced Instrument & System Integration ationConfigure and support instrument interfaces between LabWare 8 and a variety of laboratory sys tems.May develop or support parsing scripts, where required and permitted by organizational standards and govern ance.Support connectivity and data flow between LabWare and other GMP systems, such as Operational Readiness & Execution utionSupport stable execution of raw material and equipment workflows in live operat ions.Troubleshoot configuration and integration issues impacting laboratory execu tion.Partner with site teams to ensure LabWare configurations are fit for intended use and operationally sustain Required Qualifications Proven hands-on experience configuring LabWare LIMS (LabWare 8 strongly preferred). Strong experience with LabWare within GMP laboratory operations, particularlly:Raw materials te stingCommercial product te stingLaboratory equipment work flowsDemonstrated ability to translate regulatory and quality requirements into compliant LIMS configurat ions.Experience supporting LIMS validation with full requirements traceabi Preferred Qualifications Experience supporting LabWare upgrades or major LIMS implementat ions.Experience working in biopharmaceutical or pharmaceutical GMP environm ents.Experience supporting inspection readiness activities related to Deliverables & Success Criteria eria:Completed on-time LabWare LIMS configurations for raw materials, commercial products, and equipment integra tion.Clear requirements-to-configuration-to-validation traceabi lity.Stable, compliant execution of configured workflows in operat ions.Successful integration between LabWare and laboratory instrum Additional Notes notes:This role requires close collaboration with Quality, Validation, IT, and Laboratory t eams.Work must follow organizational change control, validation, and data integrity requirements. Onsite presence may be required based on project phase and site ne eds.This role will focus on validation document generation and liaison with onsite #J-18808-Ljbffr