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Lims Validation Jobs in California (NOW HIRING)

PB consulting

Support validation activities, documentation, and requirements traceability. * Troubleshoot ... Hands-on experience with LabWare LIMS, preferably LabWare 8. * Experience configuring LIMS in a GMP ...

PB consulting

Support validation activities, documentation, and requirements traceability. * Troubleshoot ... Hands-on experience with LabWare LIMS, preferably LabWare 8. * Experience configuring LIMS in a GMP ...

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Lims Validation information

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$22

$51

$77

How much do lims validation jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for lims validation in California is $51.32, according to ZipRecruiter salary data. Most workers in this role earn between $38.89 and $62.40 per hour, depending on experience, location, and employer.

What is LIMS validation?

LIMS validation is the process of ensuring that a Laboratory Information Management System (LIMS) meets regulatory requirements and performs as intended. This involves documented testing of the software to confirm its accuracy, reliability, and consistent intended performance in a specific laboratory environment. Validating a LIMS is crucial for compliance with standards such as FDA 21 CFR Part 11 or ISO 17025, and helps ensure data integrity and traceability. The process typically includes risk assessment, protocol development, execution, and documentation of results. Proper validation reduces the risk of errors and supports laboratory operations and audits.

What are the key skills and qualifications needed to thrive as a LIMS validation specialist?

To excel as a LIMS Validation Specialist, you need a strong background in laboratory processes, software validation, and knowledge of regulatory requirements, often supported by a degree in life sciences or IT. Familiarity with Laboratory Information Management Systems (LIMS), validation protocols (IQ/OQ/PQ), and tools like SQL or scripting languages is typically required. Attention to detail, problem-solving ability, and effective communication are crucial soft skills for ensuring compliance and collaborating with cross-functional teams. These competencies are vital to guarantee data integrity, regulatory compliance, and the successful implementation of LIMS in laboratory environments.

What are some common challenges faced when validating a Laboratory Information Management System (LIMS), and how can they be addressed?

One common challenge in LIMS validation is ensuring the system meets both regulatory compliance and the specific needs of the laboratory. This often requires close collaboration with IT, QA, and lab staff to gather and translate user requirements into testable validation protocols. Another challenge is managing software updates or customizations without disrupting validated processes. Staying organized with thorough documentation and leveraging validation templates can help streamline the process and ensure ongoing compliance. Open communication and regular training within the validation team are also key to addressing unexpected issues efficiently.

What is the difference between Lims Validation vs Lims Analyst?

AspectLims ValidationLims Analyst
CertificationsGxP, 21 CFR Part 11 compliance, validation certificationsGxP, 21 CFR Part 11 familiarity, relevant certifications
Work EnvironmentQuality assurance, validation teams, regulated labsLaboratories, data analysis, system monitoring
Industry UsagePharmaceutical, biotech, clinical labsLaboratory operations, data management

While Lims Validation focuses on ensuring Laboratory Information Management Systems meet regulatory standards through validation processes, Lims Analysts primarily handle data analysis, system monitoring, and supporting laboratory operations. Both roles require familiarity with GxP regulations, but Lims Validation is more specialized in validation procedures, whereas Lims Analysts focus on data integrity and system performance.

What are popular job titles related to Lims Validation jobs in California?

For Lims Validation jobs in California, the most frequently searched job titles are:

What job categories do people searching Lims Validation jobs in California look for?

The top searched job categories for Lims Validation jobs in California are:

Lims Validation jobs near you
Infographic showing various Lims Validation job openings in California as of August 2026, with employment types broken down into 60% Full Time, 7% Part Time, and 33% Contract. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

LabWare LIMS Configuration Specialist

Agoura Hills, CA • On-site

PB consulting
See more jobs at PB consultingexternal

Full-time

This job post has expired 8 days ago. Applications are no longer accepted.

Job description

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

Roles and Responsibilities
  • Configure LabWare 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 LabWare LIMS, preferably LabWare 8.
  • Experience configuring LIMS in a GMP laboratory environment.
  • Experience with raw materials, commercial product testing, and laboratory equipment workflows.
  • Experience integrating LabWare 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 LabWare upgrades or large-scale implementations.
  • Experience in pharmaceutical, biotechnology, or life sciences environments.
  • Experience supporting GMP inspections and audit readiness.

Apply