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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 14, 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 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 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 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 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 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 1% As Needed, 86% Full Time, 5% Part Time, 2% Temporary, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

LabWare 8 LIMS Configuration & Integration Specialist

Stark Pharma Solutions Inc

Thousand Oaks, CA • On-site

Contractor

Posted 24 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on LabWare 8 LIMS Specialist position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: LabWare 8 LIMS Configuration & Integration Specialist

Location: Thousand Oaks, CA (Hybrid)
Duration: 8-Month Contract
Experience: 7+ Years

Job Overview

We are seeking an experienced LabWare 8 LIMS Configuration & Integration Specialist to support GMP laboratory operations through the configuration, integration, and validation of LabWare 8 LIMS. The ideal candidate will have hands-on experience implementing compliant LIMS workflows, integrating laboratory instruments, and supporting validation activities in a regulated pharmaceutical or biopharmaceutical environment.

Key Responsibilities

  • Configure and customize LabWare 8 LIMS to support GMP laboratory operations.
  • Implement LIMS workflows for raw material testing, commercial product testing, and laboratory equipment integration.
  • Translate regulatory and quality requirements into compliant LabWare configurations.
  • Support LIMS validation activities, ensuring complete traceability from requirements through configuration and validation.
  • Integrate LabWare with laboratory instrument systems such as Empower, LabX, and other analytical platforms.
  • Troubleshoot and optimize configured workflows to ensure stable and compliant laboratory operations.
  • Collaborate with QA, QC, Validation, IT, and laboratory teams to support implementation and ongoing system enhancements.
  • Assist with inspection readiness and ensure compliance with GMP and regulatory expectations.

Required Qualifications

  • 7+ years of experience in pharmaceutical or biopharmaceutical GMP environments.
  • Hands-on experience configuring LabWare 8 LIMS.
  • Proven experience implementing LIMS solutions for raw materials, commercial products, and laboratory workflows.
  • Strong knowledge of GMP laboratory operations and regulatory compliance.
  • Experience supporting LIMS validation with end-to-end requirements, configuration, and validation traceability.
  • Experience integrating LabWare with instrument systems such as Empower, LabX, or similar platforms.
  • Excellent communication and cross-functional collaboration skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com