LabWare LIMS Configuration & Integration Specialist
Job in
Northern, Floyd County, Kentucky, USA
Listed on 2026-09-27
Listing for:
Intone Inc
Full Time
position Listed on 2026-09-27
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Job Description & How to Apply Below
Location: Northern
This is a 9-month contract position based in Thousand Oaks, California, seeking a Lab Ware LIMS 8.0 Configuration & Integration Specialist to configure and integrate laboratory information management systems in a regulated pharmaceutical or biopharmaceutical environment.
Responsibilities- Configure Lab Ware LIMS 8.0 for raw materials testing, commercial product testing, and equipment integration workflows
- Translate regulatory and quality requirements into compliant LIMS configurations
- Support LIMS validation activities, maintaining full traceability from requirements through configuration to validation
- Integrate Lab Ware systems with laboratory instrument platforms (e.g., Empower, LabX)
- Execute and stabilize configured workflows in operational GMP laboratory environments
- Support inspection readiness activities and regulatory compliance documentation related to LIMS
- Communicate cross-functionally with laboratory, quality, and IT teams in regulated environments
- Required
- Hands-on, demonstrated experience configuring Lab Ware LIMS 8.0
- Track record of completing on-time Lab Ware LIMS configurations for raw materials, commercial products, and equipment integration
- Strong experience with Lab Ware in GMP laboratory operations, including raw materials testing, commercial product testing, and laboratory equipment workflows
- Ability to translate regulatory and quality requirements into compliant LIMS configurations
- Experience supporting LIMS validation with full requirements-to-configuration-to-validation traceability
- Experience integrating Lab Ware with instrument systems such as Empower and LabX
- Experience executing stable and compliant configured workflows in operations
- Strong cross-functional communication skills in regulated environments
- Preferred
- Experience working in biopharmaceutical or pharmaceutical GMP environments
- Experience supporting inspection readiness activities related to LIMS
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