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Computer System Validation Remote Jobs (NOW HIRING)

Emvia, Inc.

Automation Validation Lead

Andover, MA · On-site +1

Automation Validation Lead Location : Andover, MA Duration - 6 months (possible extension ... computer system software and hardware: Windows operating systems Windows Terminal Services/Remote ...

Vaxcyte

Manager, IT Quality & Compliance

San Carlos, CA · On-site +1

Execute Computer Software Assurance (CSA) and Computer System Validation (CSV) activities for GxP ... Open to Remote; San Carlos, CA Compensation: The compensation package will be competitive and ...

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

As of Jun 25, 2026, the average hourly pay for computer system validation remote in the United States is $54.32, according to ZipRecruiter salary data. Most workers in this role earn between $41.83 and $64.42 per hour, depending on experience, location, and employer.

What is computer system validation (CSV) in a remote job context?

Computer system validation (CSV) is a process used to ensure that IT systems and software used in regulated industries (such as pharmaceuticals or healthcare) work as intended and comply with relevant regulations. In a remote job context, CSV professionals perform validation tasks, documentation, and system testing from an offsite location, often collaborating with teams via digital tools. This remote work typically involves reviewing validation protocols, writing reports, and ensuring compliance with standards like FDA 21 CFR Part 11, all while leveraging secure online platforms to communicate and manage documentation.

What are the key skills and qualifications needed to thrive as a Computer System Validation (CSV) professional working remotely, and why are they important?

To excel as a Computer System Validation Remote professional, you need a solid understanding of regulatory compliance (such as FDA 21 CFR Part 11), risk management, and validation lifecycle processes, often supported by a degree in computer science, engineering, or a related field. Familiarity with validation software, quality management systems (QMS), and documentation tools is typically required, along with certifications like GAMP or Six Sigma being advantageous. Strong attention to detail, analytical thinking, and effective remote communication are crucial soft skills for this role. These competencies ensure validated systems meet compliance standards, minimize risks, and support seamless collaboration in a regulated, distributed environment.

What is the difference between Computer System Validation Remote vs Computer System Validation on-site?

AspectComputer System Validation RemoteComputer System Validation on-site
Work EnvironmentPerforms validation tasks remotely, often from home or a different location from the client site.Works directly at the client or company site, conducting validation activities in person.
Required CredentialsTypically requires certifications like GxP, 21 CFR Part 11, and validation experience, applicable in both settings.Same certifications as remote roles, with additional familiarity with on-site equipment and facilities.
Industry UsageCommon in industries like pharmaceuticals and biotech where remote oversight is feasible.Traditional in regulated industries requiring on-site validation activities.

Both roles require similar certifications and industry knowledge, but the main difference lies in the work environment—remote versus on-site. Remote validation offers flexibility, while on-site validation involves direct interaction at the facility.

What are some common challenges faced by Computer System Validation professionals working remotely, and how can they be addressed?

Remote Computer System Validation (CSV) professionals often encounter challenges such as coordinating validation activities across distributed teams and ensuring secure access to sensitive documentation. Effective communication and use of collaborative tools are crucial for managing documentation reviews, test execution, and issue resolution. Establishing clear validation protocols and regular virtual check-ins with cross-functional teams can help maintain compliance and project momentum. Additionally, leveraging secure cloud-based validation platforms can streamline approvals and maintain data integrity while working remotely.
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Computer System Validation Remote jobs near you

LabWare 8 LIMS Configuration & Integration Specialist

Stark Pharma Solutions Inc

Irvine, CA • Remote

Contractor

Posted 20 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.