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Computer System Validation Csv Remote Jobs in Los Angeles, CA

Amgen

Principal Software Engineer

Thousand Oaks, CA · On-site +1

$153K - $181K/yr

Participating in and support Computer System Validation (CSV) activities, including creation and ... Flexible work models, including remote and hybrid work arrangements, where possible Apply now and ...

YO AI Labs

Autodesk Inventor Expert - Remote

Los Angeles, CA · On-site +1

$30 - $120/hr

... AI systems by creating, reviewing, and refining mechanical CAD models and technical documentation ... Create, interpret, and validate detailed engineering drawings in accordance with ASME Y14.5 (or ...

American Health Connection

Be Seen First

Human Resources Recruiter

Beverly Hills, CA · Remote

$25/hr

... remote. Since 2009, American Health Connection has supported medical health systems with full ... Strong computer skills and experience in Microsoft Office - Proficient in MS Word, Excel, and ...

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Computer System Validation Csv Remote information

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$11

$58

$92

How much do computer system validation csv remote jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for computer system validation csv remote in Los Angeles, CA is $58.53, according to ZipRecruiter salary data. Most workers in this role earn between $45.05 and $69.42 per hour, depending on experience, location, and employer.

What is the difference between Computer System Validation Csv Remote vs Computer Validation Specialist?

AspectComputer System Validation Csv RemoteComputer Validation Specialist
CertificationsGxP, 21 CFR Part 11, CSV certificationsGxP, 21 CFR Part 11, CSV certifications
Work EnvironmentRemote, regulated industries like pharma and biotechOn-site or hybrid in regulated industries
Industry UsagePharmaceutical, biotech, medical devicesPharmaceutical, biotech, medical devices
Job FocusValidating computer systems and software complianceValidating computer systems and software compliance

Both roles require similar certifications and work in regulated industries like pharma and biotech. The main difference is that Computer System Validation Csv Remote typically involves remote work, focusing on validating computer systems remotely, while Computer Validation Specialist may work on-site or in hybrid settings. Both roles aim to ensure compliance with industry standards and regulations.

What are the most commonly searched types of Computer System Validation Csv jobs in Los Angeles, CA?

The most popular types of Computer System Validation Csv jobs in Los Angeles, CA are:

What are popular job titles related to Computer System Validation Csv Remote jobs in Los Angeles, CA?

For Computer System Validation Csv Remote jobs in Los Angeles, CA, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Csv Remote jobs in Los Angeles, CA look for?

The top searched job categories for Computer System Validation Csv Remote jobs in Los Angeles, CA are:

What cities near Los Angeles, CA are hiring for Computer System Validation Csv Remote jobs?

Cities near Los Angeles, CA with the most Computer System Validation Csv Remote job openings:

Computer System Validation Csv Remote jobs near you
Infographic showing various Computer System Validation Csv Remote job openings in Los Angeles, CA as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $121,740 per year, or $58.5 per hour.

LabWare 8 LIMS Configuration & Integration Specialist

Stark Pharma Solutions Inc

Irvine, CA • Remote

Contractor

Re-posted 5 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

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.

Role: LabWare 8 LIMS Configuration & Integration Specialist

Location: Remote (California-Based Project)

Duration: Through March 2027 (Potential Extension)

Position Overview

We are seeking an experienced LabWare 8 LIMS Configuration & Integration Specialist to support a large-scale LabWare 8 upgrade initiative within a GMP-regulated pharmaceutical laboratory environment. This role will lead critical workstreams focused on configuring raw material and commercial product testing workflows, master data management, equipment integration, and validation support.

The ideal candidate will have extensive hands-on experience with LabWare 8 configuration, laboratory system integrations, and GMP laboratory operations, with the ability to deliver compliant and scalable LIMS solutions.

Key Responsibilities

  • Configure and implement LabWare 8 LIMS workflows supporting raw material and commercial product testing processes.
  • Lead master data configuration and management activities to support laboratory operations.
  • Design, configure, and optimize laboratory workflows while ensuring compliance with GMP and regulatory requirements.
  • Support integration of LabWare 8 with laboratory instrumentation and enterprise systems.
  • Collaborate with Quality, Validation, Laboratory Operations, and IT teams to ensure successful project execution.
  • Translate business, quality, and regulatory requirements into compliant LIMS configurations.
  • Support system validation activities, ensuring complete requirements-to-configuration-to-validation traceability.
  • Troubleshoot configuration, workflow, and integration issues while driving timely resolution.
  • Assist with user acceptance testing (UAT), system testing, and deployment activities.
  • Support inspection readiness efforts and ensure compliance with regulatory expectations for computerized systems.
  • Provide technical guidance and documentation throughout the project lifecycle.

Required Qualifications

  • 8+ years of experience working with Laboratory Information Management Systems (LIMS).
  • Strong hands-on experience configuring and implementing LabWare 8 LIMS.
  • Proven experience supporting LabWare upgrades, implementations, or enhancement projects.

Experience configuring workflows for:

  • Raw Material Testing
  • Commercial Product Testing
  • Laboratory Equipment and Instrument Workflows
  • Demonstrated experience supporting GMP-regulated laboratory environments.
  • Experience integrating LabWare with laboratory instruments and enterprise systems.
  • Strong understanding of computerized system validation (CSV) principles and documentation requirements.
  • Experience supporting validation deliverables with end-to-end traceability.
  • Excellent communication and stakeholder management skills within regulated environments.