LIMS Developer-Analyst

Motion Recruitment; Thousand Oaks (CA); Hybrid; USD 100,000 - 140,000; Full time

Job summary

Motion Recruitment seeks a LabWare LIMS Developer (Contract-to-Hire) to support and enhance laboratory systems in a regulated GxP environment. You will design, configure, and support LabWare LIMS v7 solutions and lead integrations with ERP, MES, and CMMS across multiple sites.

Responsibilities include CSV documentation, validation activities, and ensuring data integrity while providing L2/L3 support and CAPA investigations. Hybrid/remote options with travel are available.

Qualifications

• 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 CSV validation/documentation and regulated CSV processes (CSV) in GxP environments.

Responsibilities

• Design, configure, and support LabWare LIMS v7 solutions across sites.
• Develop and support integrations with ERP, MES, CMMS, and other enterprise systems.
• Provide L2/L3 support, troubleshooting, and root cause analysis.
• Lead change controls, deviation investigations, and CAPA activities.
• Author and maintain CSV documentation (URS, FS/DS, IQ/OQ, testing, traceability).
• Partner with QA, QC, Validation, and IT to ensure GxP/data integrity compliance.

Skills

LabWare LIMS v7

LIMS configuration

LSL scripting

Workflows

Integrations

CSV documentation

GxP/compliance

L2/L3 support

Stakeholder management

Documentation

Tools

LabWare

ServiceNow

Veeva

Git

Job description

LabWare LIMS Developer (Contract-to-Hire)

Location: Hybrid (Thousand Oaks, CA - 3 days/week preferred) or Remote with 10-25% travel

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.

Key Responsibilities

• 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.

Required Qualifications

• 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.