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LabWare LIMS Configuration Specialist

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Veriipro
Full Time position
Listed on 2026-08-07
Job specializations:
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 110000 - 170000 USD Yearly USD 110000.00 170000.00 YEAR
Job Description & How to Apply Below

We are seeking an experienced

LabWare LIMS Configuration & Integration Specialist to configure, implement, and support Lab Ware LIMS 8 in a GMP laboratory environment. The ideal candidate will have expertise in Lab Ware configuration, laboratory workflows, system integrations, and validation within regulated pharmaceutical or life sciences organizations.

Roles and Responsibilities
  • Configure Lab Ware LIMS 8 for raw materials, commercial products, stability testing, and laboratory workflows.
  • Configure master data, product specifications, sampling plans, and laboratory equipment.
  • Support integrations with laboratory instruments and systems such as Empower, LabX, and other GMP applications.
  • Translate business and regulatory requirements into compliant LIMS configurations.
  • Support validation activities, documentation, and requirements traceability.
  • Troubleshoot configuration and integration issues and support production operations.
  • Collaborate with laboratory, quality, validation, and IT teams on system enhancements and deployments.
Required Qualifications
  • Hands-on experience with Lab Ware LIMS, preferably Lab Ware 8.
  • Experience configuring LIMS in a GMP laboratory environment.
  • Experience with raw materials, commercial product testing, and laboratory equipment workflows.
  • Experience integrating Lab Ware with laboratory instruments and enterprise systems.
  • Knowledge of LIMS validation, regulatory compliance, and requirements traceability.
  • Strong troubleshooting, communication, and collaboration skills.
Preferred Qualifications
  • Experience with Lab Ware upgrades or large-scale implementations.
  • Experience in pharmaceutical, biotechnology, or life sciences environments.
  • Experience supporting GMP inspections and audit readiness.
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