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In Lims Validation Jobs in California (NOW HIRING)

CareDx, Inc.

Staff Software Engineer

Brisbane, CA · On-site

... with validation documentation and regulated software development. • Experience working in agile development environments. • Exposure to cloud-based LIMS or SaaS laboratory platforms. Company

CareDx, Inc.

Staff Software Engineer

Brisbane, CA · On-site

Familiarity with validation documentation and regulated software development. * Experience working in agile development environments. * Exposure to cloud-based LIMS or SaaS laboratory platforms. What ...

CareDx, Inc.

Staff Software Engineer

Brisbane, CA · On-site

Familiarity with validation documentation and regulated software development. * Experience working in agile development environments. * Exposure to cloud-based LIMS or SaaS laboratory platforms. What ...

kindeva

Quality Control LIMS Analyst

Northridge, CA

$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

$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 ...

Natera

Associate Scientist, R&D

San Carlos, CA · Hybrid

... validation activities. You will engage deeply in the scientific process, conduct meticulous ... in LIMS, database queries for accurate tracking and verification * Conduct independent ...

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All JobsIn Lims Validation JobsIn Lims Validation Jobs in California

In Lims Validation information

What is the difference between In Lims Validation vs Laboratory Technician?

AspectIn Lims ValidationLaboratory Technician
CertificationsGMP, GLP, Validation certificationsTypically relevant certifications include Lab Technician or related training
Work EnvironmentQuality assurance, validation labs, regulated industriesLaboratories performing tests and experiments
Job FocusEnsuring LIMS systems meet regulatory standardsPerforming tests, recording data, maintaining lab equipment

In Lims Validation professionals focus on validating Laboratory Information Management Systems to ensure compliance with industry standards, while Laboratory Technicians perform routine testing and data collection. Both roles are essential in regulated labs but differ in scope and responsibilities.

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In Lims Validation jobs near you

Labware LIMS Validation Specialist

Intellectt INC

Thousand Oaks, CA • On-site

Contractor

Re-posted 8 days ago

Job description

Job Title: Lab Ware LIMS Validation Specialist
Location: Thousand Oaks, CA -Hybrid
Duration: 12+ Months Contract

Job Summary:
Seeking an experienced Lab Ware LIMS Validation Specialist to support validation activities for laboratory systems in a regulated pharmaceutical environment. The role focuses on Computer System Validation, Lab Ware LIMS compliance, and ensuring alignment with GMP, GxP, FDA, 21 CFR Part 11, GAMP 5, and internal quality standards.

Key Responsibilities:

  • Execute validation activities for Lab Ware LIMS in compliance with GxP, FDA, and industry regulations.
  • Author, review, and execute validation documents including URS, Risk Assessments, IQ, OQ, PQ, Traceability Matrix, and Validation Summary Reports.
  • Collaborate with business, quality, and IT teams to gather and document system requirements.
  • Support change controls, deviations, CAPAs, and periodic reviews related to Lab Ware LIMS.
  • Ensure compliance with 21 CFR Part 11, GAMP 5, and internal quality standards.
  • Participate in system upgrades, enhancements, and remediation activities.
  • Provide validation support during audits and inspections.

Skills Required:

  • 5+ years of Computer System Validation experience in pharmaceutical or biotechnology environments.
  • Hands-on experience validating Lab Ware LIMS applications.
  • Strong knowledge of GxP, GMP, FDA regulations, 21 CFR Part 11, and GAMP 5.
  • Experience preparing and executing validation documentation such as URS, IQ, OQ, PQ, Risk Assessments, Traceability Matrix, and Validation Summary Reports.
  • Strong understanding of change controls, deviations, CAPAs, and periodic review processes.
 

For more information, please reach out at 732-719-4936 or share your updated resume with padma.priya@intellectt.com.