6+ Months We are currently looking for a LabWare LIMS Configuration & Integration Specialist to support a LabWare 8 upgrade within a GMP laboratory environment. Key Focus The ideal candidate will have hands-on LabWare LIMS 8 configuration experience , particularly with: Raw material and commercial product workflows LabWare master data configuration Laboratory equipment workflows Instrument/system integrations LIMS validation and requirements traceability GMP laboratory operations Key Responsibilities Configure and support LabWare 8 workflows for raw materials and commercial products, including stability. Manage master data, test workflows, specifications, sampling plans, and laboratory equipment configurations. Translate regulatory, quality, and operational requirements into compliant LabWare designs. Support LIMS validation , documentation, and requirements-to-configuration traceability. Configure and support instrument interfaces between LabWare and laboratory systems. Support integrations with systems such as Empower and LabX . Support parsing scripts where required and permitted. Troubleshoot LabWare configuration and integration issues. Partner with Quality, Validation, IT, and Laboratory teams. Ensure configurations comply with GMP, change control, validation, and data integrity requirements . Required Qualifications Proven hands-on experience with LabWare LIMS , with LabWare 8 strongly preferred . Experience working in GMP pharmaceutical/biopharmaceutical laboratory environments . Strong experience with raw material and commercial product testing. Experience configuring laboratory equipment and workflows. Experience translating business, quality, and regulatory requirements into LIMS configurations. Experience supporting LIMS validation and requirements traceability . Experience integrating LabWare with laboratory instruments/systems such as Empower or LabX . Strong communication and cross-functional collaboration skills. Preferred Qualifications LabWare 8 upgrade or major LIMS implementation experience. Pharmaceutical/biopharmaceutical GMP experience. Experience supporting LIMS inspection readiness. Experience with instrument interfaces, parsing, and laboratory data integration. apolis2024