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# LIMS Developer-Analyst

- **Company:** Kelly Services Inc.
- **Location:** Thousand Oaks, CA, United States
- **Experience:** Expert
- **Salary:** $126,880.0 - $166,400.0
- **Contract:** Temporary to permanent
- **Skills:** Agile Methodology, Computerized Maintenance Management Systems, Data Integrity, Laboratory Information Management Systems, System Testing, Systems Integration, Scripting, Enterprise Software Applications, Git, Veeva, GXP, Servicenow
- **Published:** October 8, 2026
- **Apply:** https://dejobs.org/x/x/7C11AC206B0A493E9425623B6D76A1F8/job/

## About the Role

* 5+ years of LabWare LIMS v7 development experience in Pharma, Biotech, or Cell Therapy environments.
 * Strong expertise in LabWare configuration, LIMS Basic/LSL scripting, workflows, reporting, and integrations.
 * Experience with computerized system validation (CSV), change management, and regulated GxP environments.
 * Hands-on experience supporting LIMS integrations and troubleshooting complex production issues.
 * Strong communication, documentation, and stakeholder management skills.

Preferred

 * LabWare certifications.
 * Experience with ServiceNow, Veeva, Git, and Agile delivery methodologies.

Type: Full-Time Contract with potential for permanent conversion. Visa Sponsorship is not available.

## Description

We are seeking an experienced LabWare LIMS v7 Developer to support and enhance laboratory systems in a regulated GxP environment. This role will be responsible for LIMS development, system integrations, L2/L3 support, validation documentation, and ongoing operational support across multiple Life Sciences sites., * Design, configure, and support LabWare LIMS v7 solutions, including Sample Management, Stability, Environmental Monitoring, Inventory, Raw Materials, and CoA workflows.

 * Develop and support integrations with ERP, MES, CMMS, and other enterprise systems.
 * Provide L2/L3 support, troubleshooting, root cause analysis, and system enhancements.
 * Lead change controls, deviation investigations, and CAPA activities.
 * Author and maintain CSV documentation including URS, FS/DS, IQ/OQ, testing, and traceability documentation.
 * Partner with QA, QC, Validation, and IT teams to ensure compliance with GxP, 21 CFR Part 11, and data integrity requirements.