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Lims Validation Jobs in California (NOW HIRING)

Veracyte

Manager, LIMS

San Diego, CA · On-site

$169K - $181K/yr

As the Manager, LIMS, you will lead the administration, enhancement, and operational excellence of ... Oversee system configuration, validation, implementation, release management, and ongoing ...

kindeva

Quality Control LIMS Analyst

Northridge, CA · On-site

$25.75 - $34.75/hr

The Impact You Will Make We have a great opportunity as a LIMS Analyst at our site in Northridge ... Experience leading systems improvement, validation activities or audit support efforts * Knowledge ...

kindeva

Quality Control LIMS Analyst

Northridge, CA · On-site

$25.75 - $34.75/hr

The Impact You Will Make We have a great opportunity as a LIMS Analyst at our site in Northridge ... Experience leading systems improvement, validation activities or audit support efforts * Knowledge ...

kindeva

Quality Control LIMS Analyst

Northridge, CA · On-site

$25.75 - $34.75/hr

The Impact You Will Make We have a great opportunity as a LIMS Analyst at our site in Northridge ... Experience leading systems improvement, validation activities or audit support efforts * Knowledge ...

kindeva

Quality Control LIMS Analyst

Northridge, CA · On-site

$25.75 - $34.75/hr

The Impact You Will Make We have a great opportunity as a LIMS Analyst at our site in Northridge ... Experience leading systems improvement, validation activities or audit support efforts * Knowledge ...

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Showing results 21-40

All JobsLims Validation JobsLims Validation Jobs in California

Lims Validation information

See California salary details

$22

$51

$77

How much do lims validation jobs pay per hour?

As of Aug 23, 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 & Integration Specialist (LabWare 8)

Sunrise Systems, Inc.

Thousand Oaks, CA • On-site

$90/hr

Other

Medical, Dental, Vision

Posted 29 days ago

Job description

Job Title: LabWare LIMS Configuration & Integration Specialist (LabWare 8)
Job ID:26-03584 Location: Newbury Park (Thousand Oaks), CA Duration: 8 Months
Job Summary

  • LabWare LIMS Configuration Specialist to support the LabWare 8 upgrade for a USbased GMP laboratory site. This role will lead a dedicated workstream focused on implementing raw material and commercial product workflows, completing master data configuration, and finalizing integration with laboratory equipment and enterprise GMP systems.
  • The successful candidate will translate regulatory, quality, and operational requirements into standardized, compliant LabWare LIMS designs and ensure stable execution of configured workflows in a regulated manufacturing environment.

Key Responsibilities Workstream Leadership & Scope Definition
Support a dedicated workstream supporting implementation of raw material and commercial product processes within LabWare LIMS 8.

  • Define and manage LabWare build across:
  • Raw materials and commercial product master data
  • Test workflows
  • Laboratory equipment and interfaces

LabWare LIMS Configuration
Configure raw materials, commercial products including stability, and laboratory equipment in LabWare LIMS using standardized, compliant design patterns.
Ensure LabWare configuration aligns with:

  • Approved test methodologies
  • Product specifications
  • Sampling plans

Apply controlled build practices and normalized templates to ensure consistency, scalability, and compliance.
Requirements Traceability & Validation Support

  • Translate regulatory, quality, and operational requirements into standardized LabWare LIMS designs.
  • Support validation activities by providing clear documentation and traceability for configured LabWare objects following Takeda internal procedures.

Instrument & System Integration

  • Configure and support instrument interfaces between LabWare 8 and a variety of laboratory systems.
  • May develop or support parsing scripts, where required and permitted by Takeda standards and governance.
  • Support connectivity and data flow between LabWare and other GMP systems, such as LabX

Operational Readiness & Execution

  • Support stable execution of raw material and equipment workflows in live operations.
  • Troubleshoot configuration and integration issues impacting laboratory execution.
  • Partner with site teams to ensure LabWare configurations are fit for intended use and operationally sustainable.

Required Qualifications

  • Proven handson experience configuring LabWare LIMS (LabWare 8 strongly preferred).
  • Strong experience with LabWare within GMP laboratory operations, particularly:
  • Raw materials testing
  • Commercial product testing
  • Laboratory equipment workflows
  • Demonstrated ability to translate regulatory and quality requirements into compliant LIMS configurations.
  • Experience supporting LIMS validation with full requirements traceability.
  • Experience integrating LabWare with:
  • Instrument systems (e.g., Empower, LabX)
  • Strong crossfunctional communication skills in regulated environments.

Preferred Qualifications

  • Experience supporting LabWare upgrades or major LIMS implementations.
  • Experience working in biopharmaceutical or pharmaceutical GMP environments.
  • Experience supporting inspection readiness activities related to LIMS.

Deliverables & Success Criteria

  • Completed on time LabWare LIMS configurations for raw materials, commercial products, and equipment integration.
  • Clear requirementstoconfigurationtovalidation traceability.
  • Stable, compliant execution of configured workflows in operations.
  • Successful integration between LabWare and laboratory instruments

Additional Notes

  • This role requires close collaboration with Takeda Quality, Validation, IT, and Laboratory teams.
  • Work must follow Takeda change control, validation, and data integrity requirements.
  • Onsite presence may be required based on project phase and site needs.

The hourly rate for this position is between $90.00 and $ 100.00 per hour.
Compensation:
Factors which may affect starting pay within this range may include [geography/market, skills, education, experience, and other qualifications of the successful candidate].

Benefits:
Sunrise offers ACA-compliant medical coverage/dental insurance/vision insurance to all employees. We also offer Sick time benefits as required per State regulations.

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