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Computer System Validation Engineer Jobs in Illinois

Argentum Medical

Validation Engineer

Geneva, IL · On-site

$110K - $130K/yr

Familiar with e-QMS systems such as QT9 POSITION SUMMARY: Oversees and executes design and process ... − Computer Skills - To perform this job successfully, an individual should be familiar with ...

Caterpillar

Test & Validation Engineer

Mossville, IL · On-site

$97K - $146K/yr

Work with design, mechatronics, systems integration, and software engineers to create, develop, and ... Degree Requirement A bachelor's degree in an accredited engineering, computer science, or materials ...

Tempus

Senior Quality Engineer

Chicago, IL · On-site +1

As a Senior Quality Engineer , you will: * Lead verification, validation and maintenance of host ... Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and ...

Tempus

Senior Quality Engineer

Chicago, IL · On-site

As a Senior Quality Engineer , you will: * Lead verification, validation and maintenance of host ... Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and ...

IT EXCEL LLC

Jr QA Tester

Sibley, IL

$55K - $58K/yr

... Computer System Validation. RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA Description : WE ...

IT EXCEL LLC

Jr QA Tester

Sibley, IL · On-site

$55K - $58K/yr

... Computer System Validation. RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA Description : WE ...

IT EXCEL LLC

JR QA TESTER

Evanston, IL · On-site

$55K - $58K/yr

... Computer System Validation. RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA Description : WE ...

IT EXCEL LLC

JR QA TESTER

Evanston, IL

$55K - $58K/yr

... Computer System Validation. RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA Description : WE ...

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Computer System Validation Engineer information

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$28

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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-Belvedere

Validation Engineer-Belvedere

Sterling Engineering Inc.

South Elgin, IL

$72K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 days ago

Job description

Validation Engineer
Belvidere, IL | Up to $100K | Employee-Owned Company
(DIRECT HIRE)
No Visa Transfers nor Visa Sponsorship

Join a growing automation manufacturer where your work directly impacts the medical device and advanced manufacturing industries.

Our client is a 100% employee-owned engineering company specializing in the design and build of custom high-speed automation assembly systems used in medical device, consumer goods, and industrial manufacturing environments. They are seeking a hands-on Validation Engineer to support commissioning, qualification, and technical documentation efforts for complex automated machinery.

This is a fully onsite opportunity in Belvidere, IL with occasional travel to the South Elgin facility as needed.

What You’ll Be Doing
  • Develop and execute DQ/IQ/OQ/PQ validation protocols in compliance with cGMP standards
  • Support FAT and SAT commissioning & qualification activities with customers
  • Create and maintain technical documentation including:
    • Functional Design Specifications
    • Software & Hardware Design Specs
    • Configuration & Vision Specs
    • Technical Manuals & Operator Guides
    • Machine Instructions & Spare Parts Documentation
  • Execute machine test cases to verify functionality and quality performance
  • Update validation documentation in Kneat Gx
  • Conduct risk assessments and FMEA activities
  • Support CE technical construction file development
What They’re Looking For
  • 2-year technical degree in engineering or related field
  • 3+ years of experience writing technical documentation in manufacturing environments
  • Experience with validation protocols and commissioning activities
  • Ability to read blueprints and develop technical documents
  • Experience with cGMP environments preferred
  • LEAN, Six Sigma, ISO, or medical device experience is a plus
Why This Opportunity Stands Out
  • Employee Stock Ownership Program (ESOP)
  • Pension Plan + 401(k) Contribution
  • Excellent medical benefits
  • Employer-paid dental, vision, disability & life insurance
  • Tuition reimbursement
  • Wellness reimbursement
  • Stable, growing organization with cutting-edge automation projects
  • Flexible Friday schedule (half days!)
Schedule: Monday–Thursday 7AM–4PM | Friday 7AM–12PM
Compensation: $72K–$100K depending on experience
Screening Questions
  1. Do you have experience writing and executing DQ/IQ/OQ/PQ validation protocols in a cGMP environment?
  2. Have you participated in FAT and SAT activities for manufacturing equipment?
  3. Do you have experience creating technical documentation such as FDS, SDS, HDS, validation protocols, or operator manuals?


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.