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Computer System Validation Engineer Jobs in Illinois

Belcan

Test Validation Engineer

Mossville, IL

$50/hr

Control Systems Engineer (Validation & Integration) 📍 Location: Mossville, IL (On-site) 📅 ... Computer Engineeri ng or related fie * ld4+ yea rs of experience i n system integration ...

Automated Systems, Inc.

Validation Engineer

Chicago, IL · On-site

$45 - $65/hr

... Systems, Inc. is seeking a Validation Engineer with a minimum of 3+ years of experience and has a ... strong understanding of validation principles to support a global pharmaceutical manufacturing ...

Caterpillar

Autonomy Validation Engineer

Mossville, IL · On-site

This generally includes onboard and offboard systems validation work that integrates with current ... Bachelor's degree in engineering or computer science, or an advanced degree (Masters or Ph.D.) in ...

Chemtech Plastics, Inc.

Validation Engineer

Elgin, IL

$85K/yr

Support quality system projects and activities such as engineering change order support and ... Prolonged periods sitting at a desk and working on a computer. * Office environment. * Must be able ...

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

As of Jun 10, 2026, the average hourly pay for computer system validation engineer in Illinois is $50.20, according to ZipRecruiter salary data. Most workers in this role earn between $37.74 and $62.40 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 is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or medical devices, meet all required standards for quality, reliability, and compliance. They create and execute validation protocols, document testing procedures, and ensure that systems operate as intended. Their work is critical for meeting regulatory requirements set by agencies like the FDA, and they collaborate closely with IT, quality assurance, and regulatory teams.

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 are popular job titles related to Computer System Validation Engineer jobs in Illinois? For Computer System Validation Engineer jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Engineer jobs in Illinois look for? The top searched job categories for Computer System Validation Engineer jobs in Illinois are:
Computer System Validation Engineer jobs near you
Infographic showing various Computer System Validation Engineer job openings in Illinois as of June 2026, with employment types broken down into 95% Full Time, 2% Part Time, 2% Contract, and 1% Nights. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $104,410 per year, or $50.2 per hour.

Validation Engineer (CQV, GMP, Life Sciences)

VBB

Chicago, IL • On-site

$70K - $100K/yr

Full-time

Posted 17 days ago

Job description

Validation Engineer (CQV, GMP, Life Sciences)
  • Location: Greater Chicago
  • Salary: $70-100K + Bonus + Benefits
  • No Sponsorship, No Relocation

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We're hiring a Validation Engineer who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.
What You'll Do
  • Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
  • Work on validation of lab systems, equipment, and utilities
  • Partner with engineering, validation teams, and lab stakeholders
  • Assist with project scheduling, coordination, and resource planning
  • Support commissioning & qualification (CQV) activities across projects
  • Contribute to GMP / GxP documentation and compliance efforts
  • Learn to lead validation workstreams and progress into a Validation Project Lead role
What We're Looking For
  • 5+ years of experience in:
    • Validation Engineering
    • CQV (Commissioning, Qualification, Validation)
    • or GMP-regulated environments (Pharma / Biotech)
  • Strong understanding of:
    • GMP / GxP / FDA regulations
    • Validation lifecycle (IQ/OQ/PQ)
  • Ability to work cross-functionally with engineering, QA, and operations teams
  • Strong communication and problem-solving skills
  • Coachable, driven, and motivated to grow into leadership
Requirements
  • Bachelor's degree in Engineering, Life Sciences, or related field
  • Willingness to travel regionally (project-based work)
  • Experience with validation documentation, protocols, and execution
Nice to Have
  • Experience with lab systems, utilities, or manufacturing equipment validation
  • Exposure to commissioning activities (C&Q / CQV)
  • Familiarity with AI tools for validation or documentation
Why This Role
  • Hands-on experience across pharma validation projects
  • Clear path into senior validation or project leadership roles
  • Work alongside experienced engineers in regulated environments

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer
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