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Full Time Computer System Validation information

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$86

How much do full time computer system validation jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for full time computer system validation 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 the difference between Full Time Computer System Validation vs Quality Assurance Specialist?

AspectFull Time Computer System ValidationQuality Assurance Specialist
CertificationsGAMP, CSV training, GMP knowledgeISO, Six Sigma, GMP certifications
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Primary FocusValidating computer systems and softwareEnsuring overall quality processes and compliance

Full Time Computer System Validation specialists focus on verifying that computer systems meet regulatory standards, primarily in pharma and biotech sectors. Quality Assurance Specialists oversee broader quality processes, including audits and compliance. While both roles require GMP knowledge and industry certifications, CSV roles are more technical and system-specific, whereas QA roles encompass overall quality management.

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What cities are hiring for Full Time Computer System Validation jobs? Cities with the most Full Time Computer System Validation job openings:
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Full Time Computer System Validation jobs near you
Infographic showing various Full Time Computer System Validation job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 82% Physical, 1% Hybrid, and 17% Remote job distribution, with an average salary of $112,983 per year, or $54.3 per hour.
Computer Systems Validation Specialist III

Computer Systems Validation Specialist III

Lonza

Kittery, ME • On-site

Full-time

Retirement

Posted 14 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

23rd of 74 rated pharmaceutical

Job description

Computer Systems Validation Specialist III

Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.

The Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance. They conduct risk assessments, review change requests and test scripts, draft protocols, and oversee GMP documentation revisions. This role acts as the QA CSV representative for small and large-scale projects while providing technical guidance and mentorship to junior team members.

What you will get:

  • A collaborative and inclusive work environment.

  • Opportunities for career growth and development.

  • Access to cutting-edge technologies and tools.

  • Competitive compensation and benefits package.

  • 401(k) matching plan.

  • Supportive leadership and mentoring.

  • Commitment to ethical and sustainable practices.

Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

What you will do:

  • Perform all aspects of QMS process’ – Change Control, Deviations,

  • CAPAs.

  • Perform Gap assessments to identify the gaps in processes and suggest remediation plans. Initiate the right Quality records (Deviations and CAPAs) to drive the remediation plan, as needed and execute all responsibilities as CSV project lead for projects.

  • Author/Review/Approve all end to end Computer system validation life-

  • cycle deliverables/activities.

  • Schedule qualification activities and personnel to meet business,

  • manufacturing, engineering and quality objectives.

  • Revise and maintain SOPs to ensure continuous improvement and

  • compliance to GROUP/CORP procedures.

  • Perform review of Engineering documents (P&IDs, SOPs, Specifications, Submittals, etc.).

  • Support Validation requests as a CSV SME, during Customer audits and inspections.

What we are looking for:

  • Bachelor’s degree in computer science, engineering, or related field.

  • At least 3+ years of experience in computer systems validation.

  • 3+ years of Experience in working in a cGMP facility.

  • Experience with 21 CFR Part 11 and ISPE GAMP guidelines as they relate to Computer.

  • Systems Validation (especially for analytical computerized systems).

  • Works independently and in teams.

  • Background in biotech, pharma, or medical device industry.

  • Ability to work independently and on-site in Portsmouth NH.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

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