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LIMS Developer-Analyst

Kelly Services

Thousand Oaks, CA · HybridContract / Full-time$61–80/hrSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
$61–80/hr
Location
Thousand Oaks, CAHybrid
Schedule
Contract / Full-time
Work Authorization
Not specified

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Job overview

The LabWare LIMS v7 Developer supports and enhances laboratory systems in regulated GxP environments across Life Sciences sites. The role covers LIMS development, integrations, L2/L3 support, validation documentation, and operational support. It is a full-time contract-to-hire opportunity, offered hybrid in Thousand Oaks with three days per week preferred or remotely with 10–25% travel. Visa sponsorship is unavailable.

Skills & qualifications

RequiredNice to have

Skills

LabWare LIMS V7 DevelopmentLabWare ConfigurationLIMS Basic/LSL ScriptingWorkflowsReportingIntegrationsComputerized System ValidationChange ManagementTroubleshootingCommunicationDocumentationStakeholder ManagementServiceNowVeevaGitAgile Delivery

Qualifications

5+ Years LabWare LIMS V7 ExperiencePharma, Biotech, or Cell Therapy ExperienceLabWare CertificationsFull-Time Work Authorization

Full job description

$61 - $80

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.

Motion Recruitment Partners (MRP) is an Equal Opportunity Employer. All applicants must be currently authorized to work on a full-time basis in the country for which they are applying, and no sponsorship is currently available. Employment is subject to the successful completion of a pre-employment screening. Accommodation will be provided in all parts of the hiring process as required under MRP’s Employment Accommodation policy. Applicants need to make their needs known in advance.

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