Job Summary: LabWare 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 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
Product specifications
Sampling plans
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 Client’s 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 Client’s 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.
Demonstrated 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 Qualifications: Experience 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 Criteria: Completed 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 instruments
Additional Notes: This role requires close collaboration with Client’s Quality, Validation, IT, and Laboratory teams. Work must follow Client’s change control, validation, and data integrity requirements. Onsite presence may be required based on project phase and site needs.
Applicant Notices & Disclaimers
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At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position's pay range is $90.00/hr - $92.00/hr.
