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From Home Computer System Validation Jobs in Seattle, WA

Valspec

Validation Engineer (CSV)

Redmond, WA · On-site

Key Responsibilities * Lead Computer System Validation (CSV) activities for DeltaV-based ... When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from ...

Valspec

Validation Engineer (CSV)

Seattle, WA

Key Responsibilities * Lead Computer System Validation (CSV) activities for DeltaV-based ... When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from ...

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From Home Computer System Validation information

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How much do from home computer system validation jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for from home computer system validation in Seattle, WA is $61.82, according to ZipRecruiter salary data. Most workers in this role earn between $47.60 and $73.32 per hour, depending on experience, location, and employer.

What is the difference between From Home Computer System Validation vs From Home Quality Assurance Specialist?

AspectFrom Home Computer System ValidationFrom Home Quality Assurance Specialist
CertificationsGxP validation, 21 CFR Part 11ISO 9001, QA certifications
Work EnvironmentPrimarily remote, focused on system testing and validationRemote or onsite, focused on process audits and compliance
Industry UsagePharmaceutical, biotech, healthcareManufacturing, software, healthcare
Job FocusEnsuring computer systems meet regulatory standardsEnsuring overall quality processes and compliance

From Home Computer System Validation primarily involves verifying that computer systems meet regulatory standards, especially in healthcare and biotech industries. In contrast, From Home Quality Assurance Specialist focuses on broader quality processes and compliance across various industries. Both roles may be remote and require similar certifications, but their core responsibilities differ in scope and focus.

Is computer system validation a good field?

Computer system validation is a specialized field within quality assurance and regulatory compliance, primarily in industries like pharmaceuticals and healthcare. It involves ensuring that computer systems meet regulatory standards through documentation, testing, and validation protocols, often requiring knowledge of GxP regulations and validation tools. The field offers steady demand and opportunities for certification and skill development.

What are the most commonly searched types of Computer System Validation jobs in Seattle, WA?

The most popular types of Computer System Validation jobs in Seattle, WA are:

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For From Home Computer System Validation jobs in Seattle, WA, the most frequently searched job titles are:

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The top searched job categories for From Home Computer System Validation jobs in Seattle, WA are:

From Home Computer System Validation jobs near you
Infographic showing various From Home Computer System Validation job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 23% Part Time, and 4% Contract. Highlights an 79% Physical, 1% Hybrid, and 20% Remote job distribution, with an average salary of $128,577 per year, or $61.8 per hour.

Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

Bothell, WA • On-site

Other

Posted 2 days ago

New

Job description

Job Summary:
  • We are seeking an experienced Computer System Validation (CSV) Engineer/Contractor to lead and execute validation activities for GxP computerized systems, with a strong focus on Manufacturing Execution Systems (MES) in a pharmaceutical or biologics manufacturing environment.
  • The ideal candidate will have expertise in CSV lifecycle management, GAMP, 21 CFR Part 11, protocol development and execution, and cross-functional collaboration to ensure compliance with regulatory and quality requirements.

Roles & Responsibilities:
  • Lead and execute Computer System Validation (CSV) activities for GxP computerized systems and applications throughout the validation lifecycle.
  • Develop, review, execute, and maintain CSV documentation, including Validation Plans, User Requirements Specifications (URS), Functional/Design Specifications, Risk Assessments, IQ, OQ, PQ protocols, Traceability Matrices, Validation Summary Reports, and SOPs.
  • Support the validation of Manufacturing Execution Systems (MES) and ensure compliance with internal procedures and regulatory requirements.
  • Partner with Business Owners, Technical Owners, Quality Assurance (QA), Manufacturing, Engineering, and IT teams to develop validation deliverables and system requirements.
  • Assist with User Acceptance Testing (UAT) by supporting protocol execution, documenting test results, investigating test failures, and ensuring testing complies with established procedures.
  • Develop system requirements and specifications for computerized systems used in GxP manufacturing operations.
  • Perform risk-based validation activities in accordance with GAMP methodology.
  • Ensure compliance with cGMP, GxP, GAMP, SDLC, and 21 CFR Part 11 regulations governing computerized systems and electronic records.
  • Support change control, incident management, and system lifecycle activities using IT service management tools.
  • Collaborate with cross-functional teams to resolve validation issues and maintain audit-ready documentation.
  • Provide on-site support throughout User Acceptance Testing (UAT) execution.

Requirements / Qualifications:
  • Bachelor's degree in Life Sciences, Engineering, Information Technology, Computer Science, or a related discipline (or equivalent industry experience).
  • 4+ years of experience in Computer System Validation (CSV) within a GxP-regulated pharmaceutical, biotechnology, or biologics manufacturing environment.
  • Strong hands-on experience with Manufacturing Execution Systems (MES) validation (e.g., Emerson Syncade).
  • Strong understanding of Computer System Validation (CSV) principles and validation lifecycle activities.
  • Experience developing and executing CSV documentation, including:
  • Validation Plans
  • User Requirements Specifications (URS)
  • Functional/Design Specifications
  • Risk Assessments
  • IQ/OQ/PQ Protocols
  • Validation Summary Reports
  • Traceability Matrices
  • Standard Operating Procedures (SOPs)
  • Strong knowledge of GAMP 5, 21 CFR Part 11, cGMP, GxP, SDLC, and Good Documentation Practices (GDP).
  • Experience with User Acceptance Testing (UAT), protocol drafting, execution, and defect management.
  • Familiarity with ERP systems (e.g., SAP, Oracle) and Electronic Batch Records (EBR) systems (e.g., InfoBatch).
  • Experience with Quality Management Systems (e.g., Veeva) and IT Service Management tools (e.g., ServiceNow).
  • Knowledge of pharmaceutical manufacturing, laboratory systems, and biologics manufacturing processes.
  • Excellent technical writing, communication, problem-solving, and cross-functional collaboration skills.
  • Ability to work independently while managing multiple validation activities in a fast-paced, regulated environment.

Apply