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Computer System Validation Jobs in Redmond, WA (NOW HIRING)

Evote

Automation CSV Engineer - Site Based, Redmond, WA

Redmond, WA · On-site

$115 - $126.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience supporting automation validation and Computer System Validation (CSV) activities for manufacturing systems such as DeltaV, PI, SCADA, PLC, and related automation platforms is required.

New

Socket.dev

AI Cluster Validation Architect

Seattle, WA · On-site

$170 - $230/hr

As a Systems Validation and SW Architect, you will deliver our next generation of system ... Bachelor's or Master's degree in Computer Science, Computer Engineering, Electrical Engineering, or ...

New

Bristol Myers Squibb

Senior Engineer I, Validation

Bothell, WA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Robust knowledge of cGMP, GDP, GXP, GAMP5 regulations, including 21CFR part 11, computer systems validation requirements, EU GMP Annex 15, and data integrity requirements * Experience with equipment ...

Evotec

IT CSV Engineer

Redmond, WA

$115K - $135K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Collaborate with cross-functional teams to execute complex Computer System Validation (CSV) projects, including remediation and new system implementations. * Develop validation strategies and author ...

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Computer System Validation information

See Redmond, WA salary details

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How much do computer system validation jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for computer system validation in Redmond, WA is $60.83, according to ZipRecruiter salary data. Most workers in this role earn between $46.83 and $72.16 per hour, depending on experience, location, and employer.

What is a computer system validation?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in computer system validation, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in computer system validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It offers opportunities for professionals with skills in validation protocols, regulatory requirements, and tools like GxP and 21 CFR Part 11. The field provides steady employment, career growth, and the chance to work on critical quality assurance processes.

What are popular job titles related to Computer System Validation jobs in Redmond, WA?

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

What job categories do people searching Computer System Validation jobs in Redmond, WA look for?

The top searched job categories for Computer System Validation jobs in Redmond, WA are:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in Redmond, WA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $126,535 per year, or $60.8 per hour.

Validation Engineer

Katalyst Healthcares and Lifesciences

Bothell, WA • On-site

Other

Posted 5 days ago

Job description

Summary :
We are seeking an experienced Validation Engineer to support pharmaceutical manufacturing and quality operations in Washington. The ideal candidate will have hands-on experience in equipment, process, cleaning, and computerized system validation within a GMP-regulated pharmaceutical environment. This role requires strong knowledge of validation lifecycle activities, regulatory compliance, documentation, and cross-functional collaboration.
Roles & Responsibilities :
  • Execute and support validation lifecycle activities including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
  • Develop, review, and approve validation protocols, test scripts, summary reports, and related GMP documentation.
  • Perform equipment qualification for manufacturing, packaging, utilities, and laboratory systems.
  • Support process validation, cleaning validation, and revalidation activities for pharmaceutical manufacturing processes.
  • Conduct impact assessments for change controls, deviations, CAPA, and non-conformance investigations.
  • Collaborate with Quality Assurance, Manufacturing, Engineering, and Regulatory teams to ensure compliance with validation requirements.
  • Ensure validation documentation aligns with FDA, cGMP, GxP, 21 CFR Part 11, and data integrity requirements.
  • Participate in commissioning and qualification activities for new equipment and facility expansions.
  • Review calibration, maintenance, and qualification records for compliance readiness.
  • Support internal/external audits and regulatory inspections by providing validation documentation and technical expertise.
  • Maintain validation master plans, SOPs, and validation schedules.

Education & Experience :
  • Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related field.
  • 5+ years of validation experience in pharmaceutical, biotech, or life sciences industry.
  • Strong experience in IQ/OQ/PQ, process validation, cleaning validation, CSV, and equipment qualification.
  • Knowledge of FDA regulations, cGMP, GAMP 5, 21 CFR Part 11, ALCOA+, and validation lifecycle methodologies.
  • Experience with deviations, CAPA, change controls, and risk assessments.
  • Excellent documentation, analytical, and problem-solving skills.
  • Strong communication skills and ability to work cross-functionally in a fast-paced environment.
  • Experience with sterile manufacturing, aseptic processing, or biologics is a plus.
  • Familiarity with validation management systems such as TrackWise, Veeva, Kneat, MasterControl, or ValGenesis.
  • Prior experience supporting regulatory inspections or audit readiness initiatives.

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