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Computer System Validation Jobs in Arizona (NOW HIRING)

Renesas Electronics

Validation Engineer

Tempe, AZ · On-site

The ideal candidate must have hands-on experience with silicon bring-up and validation, and collaborating cross-functionally with design, system, and product engineering teams. Responsibilities ...

Renesas Electronics

Validation Engineer

Tempe, AZ · On-site

The ideal candidate must have hands-on experience with silicon bring-up and validation, and collaborating cross-functionally with design, system, and product engineering teams. Responsibilities ...

GDIT

$88K - $115K/yr

Ability to conduct system integration testing and analyze new technology sets, * Experience using enterprise lab environments for validation and assessment. Location is Onsite. GDIT IS YOUR PLACE At ...

Lunewave, Inc.

Sensor Validation Engineer

Tucson, AZ · On-site

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 ...

RD Partners

Validation Engineer

Tucson, AZ · On-site

$39 - $42/hr

R&D Partners is seeking to hire a Validation Engineer in Tucson, AZ . Your main responsibilities as a Validation Engineer: · Develop, write, review, and execute process validation/process ...

Belcan

Avionics Systems Engineer

Phoenix, AZ · Hybrid

... system validation & verification testing and certification activities. · Support System Safety ... or Computer Science. · Minimum of 5+ years of Systems Engineering experience in Avionics for ...

U-Haul

Computer Support Specialist

Tempe, AZ · On-site

Diagnose and resolve hardware, software, operating system, printer, and peripheral issues ... Valid driver's license with the ability to travel regularly between U-Haul Technical Center ...

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Computer System Validation information

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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 Arizona is $50.62, according to ZipRecruiter salary data. Most workers in this role earn between $38.99 and $60.05 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 the most commonly searched types of Computer System Validation jobs in Arizona?

The most popular types of Computer System Validation jobs in Arizona are:

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

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What cities in Arizona are hiring for Computer System Validation jobs?

Cities in Arizona with the most Computer System Validation job openings:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, 2% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $105,287 per year, or $50.6 per hour.

Validation Engineer

Katalyst Healthcares and Lifesciences

Tucson, AZ • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Job Description:
  • Client is looking for onsite Validation Engineers / CQV Engineers to support upcoming qualification work tied to sterile manufacturing and fill/finish operations. The consultants will support hands-on OQ/PQ execution, GMP documentation, protocol execution, discrepancy/deviation support, and equipment qualification activities.
  • The ideal candidate will have direct validation engineering or CQV experience in a fast-paced GMP environment, with strong exposure to fill line qualification, aseptic filling, sterile manufacturing equipment, and execution-heavy validation work. Equipment experience with autoclaves, formulation equipment, fill suites, high-velocity fillers, isolators, parts washers, tanks, and aseptic process systems is highly relevant.
  • Experience with vision systems or automated inspection systems is a strong plus, especially for candidates who have worked around high-speed fill lines or aseptic manufacturing lines. Candidates should be able to work independently onsite, execute protocols accurately, document in real time, identify discrepancies, and help drive qualification deliverables through completion.
Requirements:
  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline preferred. Equivalent hands-on validation/CQV experience in GMP manufacturing environments can be considered.
Strong Plus Skills:
  • septic Fill/Finish Equipment Experience: Exposure to isolators, high-velocity fillers, formulation equipment, fill suites, parts washers, tanks, and autoclaves.
  • Sterilization / Sterile Manufacturing Systems: Experience with SIP, VHP, autoclaves, and sterile equipment qualification.
  • Vision / Inspection System Experience: Background with vision systems or automated inspection systems, especially tied to aseptic filling or high-speed manufacturing lines.
  • Validation Tools / Execution Support: Experience using Kaye validators, wireless probes, and supporting hands-on protocol execution.
  • Documentation & Closeout: Strong ability to document execution in real time, manage discrepancies, and support protocol package closeout.
Include Must Have:
  • Hands-on validation engineering or CQV experience.
  • Strong OQ/PQ execution and documentation background.
  • Fill/finish, aseptic filling, or fill line qualification experience.
  • Sterilization or sterile manufacturing equipment experience.
  • GMP documentation experience.
  • Protocol execution experience.
  • Deviation/discrepancy support experience.
  • bility to work independently in a fast-paced project environment.
  • Experience supporting equipment qualification in a regulated life sciences environment.

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