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Computer System Validation Engineer Jobs in Arizona

Validation Engineer

Oro Valley, AZ · On-site

$39 - $42/hr

Validation Engineer Description: ***We are seeking a proactive Validation Engineer with 1-3 years ... systems. • Conducts risk assessments and develops qualification strategies for new and existing ...

Sensor Validation Engineer Who we are: Lunewave Inc. is a privately held technology company ... Bachelor's degree in engineering, computer science or physics * Experience in data analysis ...

Bachelor's degree in engineering, computer science or physics * Experience in data analysis ... Validate driver's license * Comfortable manipulating large multi-dimensional data sets

Apply Early

Bachelor's degree in computer science or equivalent. Experience with manual testing preferred * 4-7 ... debugging complex systems, including web services, API * Experience debugging LAMP stack ...

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Hardware Validation Engineer

Phoenix, AZ · On-site

$122K - $161K/yr

The Role: * A self-starter who leads the design of validation of a system during development ... Bachelors degree in electrical, mechanical, computer science or related engineering field with 5+ ...

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Computer System Validation Engineer information

See Arizona salary details

$27

$48

$70

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

As of Jul 2, 2026, the average hourly pay for computer system validation engineer in Arizona is $48.27, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $60.05 per hour, depending on experience, location, and employer.

What are some common challenges faced by Computer System Validation Engineers in regulated industries?

Computer System Validation Engineers often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for multiple systems, and ensuring timely validation while coordinating with cross-functional teams. Balancing strict compliance with project deadlines can be demanding, especially when systems are complex or legacy infrastructure is involved. Additionally, effective communication with IT, QA, and business stakeholders is essential to address issues quickly and maintain validation standards.

What does a computer system validation engineer do?

A computer system validation engineer ensures that computer systems used in regulated industries meet required standards for quality, safety, and compliance. They develop validation protocols, perform testing, document results, and ensure systems function correctly according to regulatory guidelines such as FDA or GMP. This role often involves working with validation tools, risk assessments, and maintaining detailed documentation to support audits and inspections.

What are the key skills and qualifications needed to thrive as a Computer System Validation Engineer, and why are they important?

To thrive as a Computer System Validation Engineer, you need a solid background in computer science or engineering, knowledge of regulatory requirements (such as FDA or GxP), and experience in validation processes. Familiarity with validation tools, quality management systems, and documentation software is typically required, along with certifications like ISPE or ASQ being beneficial. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for coordinating teams and ensuring compliance. These skills and qualities are crucial to ensure that computer systems meet regulatory standards, maintain data integrity, and support business operations in regulated industries.

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

AspectComputer System Validation EngineerQuality Assurance Specialist
CertificationsGAMP, GxP validation certificationsISO, Six Sigma, GMP certifications
Work EnvironmentPharmaceutical, biotech, medical device industriesManufacturing, software, healthcare sectors
Primary FocusValidating computer systems and software complianceEnsuring overall quality and process improvements

The Computer System Validation Engineer primarily focuses on validating computer systems to meet regulatory standards, ensuring software compliance in regulated industries. In contrast, the Quality Assurance Specialist oversees broader quality processes, including audits and process improvements. Both roles require knowledge of industry regulations but differ in scope and specific responsibilities.

What is the salary of SoC validation engineer?

The salary of a System on Chip (SoC) validation engineer typically ranges from $80,000 to $130,000 annually, depending on experience, location, and company size. Entry-level positions may start lower, while experienced engineers with specialized skills in hardware description languages and verification tools can earn higher salaries.

What is the salary of a CSV engineer?

The salary of a Computer System Validation (CSV) Engineer typically ranges from $70,000 to $120,000 annually, depending on experience, location, and certifications such as GxP or 21 CFR Part 11. Senior roles or those in high-cost-of-living areas may offer higher compensation, and knowledge of validation tools like MasterControl or ValGenesis can enhance earning potential.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital field in regulated industries like pharmaceuticals and biotech, ensuring software and systems meet compliance standards such as 21 CFR Part 11. It offers stable job opportunities, requires knowledge of validation protocols, and often involves working with tools like GxP guidelines and validation documentation. The field is considered stable and growing due to ongoing regulatory requirements.
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What job categories do people searching Computer System Validation Engineer jobs in Arizona look for? The top searched job categories for Computer System Validation Engineer jobs in Arizona are:
Infographic showing various Computer System Validation Engineer job openings in Arizona as of June 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $100,408 per year, or $48.3 per hour.
Validation Engineer

Validation Engineer

Motion Recruitment

Oro Valley, AZ • On-site

$39 - $42/hr

Other

Posted 15 days ago


Job description

Title: Validation Engineer

Description: ***We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive operational integrity***
***This is an on-site position that focuses on equipment validation. Pay range for this position is $39/hr-$42/hr, depending on experience***
• Experience: 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA)
• Focus: Equipment Qualification
• Employment Type: On-site position
Responsibilities
• Develops, prepares, and executes IQ, OQ, and PQ protocols and reports for equipment/systems.
• Conducts risk assessments and develops qualification strategies for new and existing equipment/systems.
• Analyzes and interprets qualification data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.
• Collaborates with cross-functional teams, including Process Engineering, Automation Maintenance Support, Design Transfer Operations, Manufacturing, Quality, Facilities, and Safety Health and Environment (SHE), to ensure seamless execution of qualification activities and successful achievement of qualification-related project milestones.
• Participates in process optimization and continuous improvement initiatives to enhance quality and efficiency.
• Ensures compliance with FDA, ISO, and other relevant regulatory guidelines, as well as adherence to internal requirements.
• Provides training and guidance to manufacturing and quality personnel on qualification processes and procedures.
• Maintains equipment/systems qualification documentation and ensures traceability and accessibility for audits and inspections.
• Other duties as assigned by management.
Qualifications
• Bachelor's Degree in Engineering or Life Science.
• Strong technical writing, analytical, and problem-solving skills.
• Knowledge of cGMP and regulatory standards.
• Demonstrated experience assisting with or supporting qualification activities within the medical device, pharmaceutical, or biotechnology industry is required.

Skills: