LabWare LIMS Developer - Remote Contract-to-Hire

**LabWare LIMS v7 Developer Pharma / Biotech GxP Environment**

Help modernize laboratory systems in a regulated life sciences environment.

Industry: Biopharma

Contract: 6-12 Months to Hire.

Contract Type: W2 (paid weekly; health and 401k benefits)

Remote: Anywhere in USA. Should be able to support EST business hours

Travel: 10%-15% domestically

We are seeking an experienced LabWare LIMS v7 Developer to support and enhance laboratory systems in a regulated Pharma/Biotech environment. This role combines hands-on LIMS development and configuration with L2/L3 production support, system integrations, and Computer System Validation (CSV).

Location: Thousand Oaks, CA, with support for Irvine, CA, and Madison, WI, as needed

Experience: 5–10 years

Environment: GxP-regulated Pharma, Biotech, or Cell Therapy

Key Responsibilities

• Develop, configure, and enhance LabWare LIMS v7 workflows for Sample Management, Batch-to-CoA, Environmental Monitoring, Raw Materials, Stability, and Inventory.
• Develop LIMS Basic/LSL scripts, calculations, templates, custom reports, BarTender labels, and instrument interfaces.
• Support LIMS integrations with ERP, MES, CMMS, and SDMS systems.
• Provide L2/L3 support, troubleshooting, root-cause analysis, performance tuning, and system upgrade support.
• Prepare and execute CSV documentation, including specifications, IQ/OQ, test scripts, impact assessments, and traceability matrices.
• Lead change controls and deviation investigations, including root-cause analysis and CAPA.
• Maintain GxP compliance, data integrity, security, and audit trails while collaborating with QC, QA, Validation, and IT.

Required Qualifications

• 5–10 years of hands-on LabWare LIMS v7 development in a GxP-regulated environment.
• Strong experience with LIMS configuration, LIMS Basic/LSL, laboratory workflows, and system integrations.
• Practical CSV experience and knowledge of 21 CFR Part 11, EU Annex 11, and ALCOA+ principles.
• Experience with L2/L3 support, change control, deviation/CAPA processes, and validated system documentation.
• Familiarity with ServiceNow and Veeva DMS/QMS.

Preferred: LabWare certifications, Git/compliant DevOps practices, and ITIL or IT Service Management experience.

• Interested in contributing your LabWare expertise to critical laboratory and quality systems? Please reach out to discuss the opportunity.