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Computer System Validation Engineer Jobs in Arizona

RXinsider LTD.

Validation Engineer and CQV

Phoenix, AZ · On-site

$60 - $80/hr

Position Summary The Validation Engineer and CQV Associate supports validation documentation, data collection, and quality system activities in Medivant's sterile injectable facility. This ...

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Computer System Validation Engineer information

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

As of Sep 4, 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 the key skills and qualifications needed to thrive as a computer system validation engineer?

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 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 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.

Are computer system validation engineers in demand?

Computer System Validation Engineers are in demand due to the increasing regulation of pharmaceutical, biotech, and medical device industries that require compliant validation of computer systems. They often need skills in validation protocols, GxP regulations, and validation tools, making their expertise valuable in ensuring quality and compliance in regulated environments.

Do computer system validation engineers make good money?

Computer System Validation Engineers typically earn competitive salaries that vary by experience, location, and industry. They often have specialized skills in validation protocols, regulatory compliance, and validation tools, which can contribute to higher earning potential. Certification and experience in regulated environments like pharmaceuticals or biotech can also impact salary levels.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital field in regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It involves skills in validation protocols, documentation, and tools like GxP regulations and audit readiness, making it a stable and in-demand career path for those with technical and regulatory knowledge.

What does a computer system validation engineer do?

A computer system validation engineer ensures that computer systems used in regulated industries, such as pharmaceuticals or biotech, meet required standards for quality and compliance. They develop validation protocols, perform testing, document results, and ensure systems function correctly and securely, often using tools like GxP guidelines and validation software. Their work helps ensure data integrity and regulatory compliance throughout the system lifecycle.

What are popular job titles related to Computer System Validation Engineer jobs in Arizona?

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

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:

Computer System Validation Engineer jobs near you
Infographic showing various Computer System Validation Engineer job openings in Arizona as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $100,408 per year, or $48.3 per hour.

Validation Engineer and CQV

RXinsider LTD.

Phoenix, AZ • On-site

$60 - $80/hr

Other

Posted 4 days ago

Job description

About Medivant Healthcare

Medivant Healthcare is a U.S.-based pharmaceutical manufacturer specializing in sterile injectable generics for hospitals, clinics, and healthcare providers nationwide. Our FDA-registered facilities in Chandler and Deer Valley, Arizona, are dedicated to ensuring consistent product quality, regulatory compliance, and affordable medication access.

Position Summary

The Validation Engineer and CQV Associate supports validation documentation, data collection, and quality system activities in Medivant's sterile injectable facility. This entry-level role is ideal for recent graduates seeking hands-on cGMP and aseptic processing experience.

Key Responsibilities
  • Assist in execution of media fill studies and documentation.
  • Support area qualification and environmental monitoring tasks.
  • Help draft IQ/OQ/PQ protocols and assist execution.
  • Collect data for HVAC, WFI, and compressed air validation.
  • Assist in cleaning validation logs and sample documentation.
  • Participate in process validation protocol preparation.
  • Support change control documentation.
  • Assist in deviation data collection and preliminary reports.
  • Track CAPA activities and closure evidence.
  • Ensure cGMP compliance in all assigned tasks.
Qualifications

Required:

  • Bachelor's degree in Pharmacy, Biotechnology, Microbiology, Life Sciences, or related field.
  • 2-3 years of relevant experience is required
  • Understanding of aseptic and sterile processing.
  • Strong documentation and communication skills.
Preferred
  • Experience in sterile manufacturing or validation support.
  • Knowledge of QMS processes and cGMP environments.
Employment Details
  • Full-time onsite role at Medivant Healthcare facilities.
  • Standard work schedule: Monday-Friday.
  • Training provided for all validation and QMS procedures.

Please note that we are not providing H1B visa sponsorship for this role. Candidates will be solely responsible for managing and maintaining their own visa sponsorship status.

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