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Full Time Computer System Validation information

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$54

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

As of Jun 24, 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 June 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 2% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $112,983 per year, or $54.3 per hour.

Computer System Validation Engineer

Scalence L.L.C.

Bothell, WA • On-site

Full-time

Posted 9 days ago

Job description

Job Summary:
Scalence L.L.C. is seeking a Computer System Validation Engineer to lead and execute validation activities for GxP electronic systems and applications. The role involves partnering with Business Owners, Technical Owners, and Quality to create and manage validation deliverables throughout the validation lifecycle.
Responsibilities:
• Author, review and/or approve applicable CSV documentation
• Assist Business Owners and Technical Owners during test execution, document test failures and ensure testing aligns with internal procedures
• Assist Business Owners and Technical Owners to develop requirements and specifications for computerized systems used in GxP operations
• Other related duties as assigned
Qualifications:
Required:
• Strong Computer Systems Validation (CSV) experience
• Familiarity with Manufacturing Execution Systems (MES)
• Protocol drafting and execution, good communication
• Required to be onsite throughout UAT execution
• Ability to effectively communicate with both technical and non-technical team members
• Strong interpersonal skills, especially regarding team work, client focus, verbal and written communication
• Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, and good documentation practices
• Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment that support Biologics and clinical manufacturing
• Knowledge of IT service management platforms to support incident, problem and change IT operational events (i.e. ServiceNow)
• Knowledge and exposure to Business Quality Management Systems (i.e. Veeva)
• Strong technical and problem-solving skills and the ability to work independently
• Demonstrated success working in a high-performing, business results-driven environment
• Understanding of computer system validation
• Familiarity with MES systems (i.e. Emerson Syncade), ERP systems (i.e. SAP or Oracle) and EBRs (i.e. InfoBatch)
• Understanding of computer system validation (CSV)
• Bachelor's degree in a life sciences or engineering / IT discipline or equivalent industry experience (a combination of industry-specific education and work experience may be used to substitute this degree requirement)
• 4+ years of direct experience with CSV activities, strong knowledge of GAMP / risk-based approaches to validation and good understanding of electronic records and signatures
• Strong knowledge on Manufacturing Execution System (MES) validation
• Strong knowledge of regulations, current industry practices, and experience with application of guidelines and regulations related to control of computerized systems, electronic records / signatures
• Strong knowledge on development of CSV documentation (Validation Plans, Requirements, Specifications, Assessments, Test Scripts [IQ / OQ / PQ or equivalent], Summary Reports, Trace Matrices, SOPs, etc.)
Company:
In today’s dynamic and competitive market, success hinges on mastering three key areas: Data Intelligence, Business Resilience, and Digital Experience. Founded in , the company is headquartered in Morristown, New Jersey, US, , with a team of 501-1000 employees. The company is currently Late Stage.

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