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Validation Engineer Jobs in Elgin, IL (NOW HIRING)

OnShore Technology Group

Sr. Validation Lead

Chicago, IL · On-site

$120 - $170/hr

The Sr. Validation Lead is primarily responsible for oversight of V&V activities for designated ... S. or equivalent in computer science, engineering, life sciences, or related field * Minimum 10 ...

Pioneer GMP Consulting

CQV Engineer (Chicago)

Chicago, IL · On-site

$110 - $150/hr

We're seeking a CQV Engineer to join our team at Pioneer GMP Consulting and support clients across ... In this role, you'll support commissioning, qualification, and validation activities across a wide ...

Deloitte

System Test and Validation Lead

Chicago, IL · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Chicago, IL · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Chicago, IL · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

Model Validation Consultant

Chicago, IL · On-site

You will execute validation activities, contribute to documentation and testing, and help teams assess model risk management practices and responsible AI deployment across industries such as ...

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Validation Engineer information

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$22

$51

$77

How much do validation engineer jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for validation engineer in Elgin, IL is $51.40, according to ZipRecruiter salary data. Most workers in this role earn between $38.99 and $62.50 per hour, depending on experience, location, and employer.

What is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

What is the difference between Validation Engineer vs Quality Assurance Engineer?

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often in regulated industries like pharmaceuticals or manufacturing. The role typically requires attention to detail, knowledge of validation protocols, and familiarity with tools like GxP or FDA regulations. It can offer stable employment and opportunities for specialization and advancement.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of industry standards and experience with validation tools are also important.
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Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Elgin, IL as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $106,910 per year, or $51.4 per hour.

Sr. Validation Lead

OnShore Technology Group

Chicago, IL • On-site

$120 - $170/hr

Other

Posted 4 days ago

Job description

For over 15 years, we have worked as a trusted partner with our clients as well as many global system integrators and technology companies to help deliver turnkey validated systems and ensure sustained compliance.

OnShore’s leading innovation is ValidationMaster™, the first Enterprise Validation Management System (EVMS) of its kind to include a validation Kanban board and seamless integration with our unique ValidationMaster Quality and Risk Management portal.

The Sr. Validation Lead is primarily responsible for oversight of V&V activities for designated computerized system implementation projects. This position requires a senior-level individual with strong experience in supporting computer system validation (CSV) efforts for applications used in GMP, GLP and/or GCP processes ensuring adherence to internal procedures, industry practices such as ISPE GAMP 5, and applicable regulations such as FDA 21 CFR Part 11, EudraLex Annex 11, SOX and cGMPs.

ROLES & RESPONSIBILITIES
  • Ability to lead and coordinate multiple CSV projects
  • Develop / review validation test protocols as required using automated technology tools
  • Coordinate / communicate with other departments, SMEs
  • Ensure that all validation deliverables are prepared in accordance with internal guidelines, policies and procedures
  • Create, track and manage all validation project plans
  • Provide regulatory guidance on principles of CSV to the expanded team
EDUCATION & CERTIFICATION
  • B.S. or equivalent in computer science, engineering, life sciences, or related field
  • Minimum 10 years of experience in software quality assurance in the life sciences industry in a leadership role
  • ASQ CSQE Certification or equivalent preferred
  • Practical working knowledge of software development and implementation methodologies
  • Experience with the validation of Enterprise Resource Planning (ERP) systems is preferred.
  • Strong oral and written communication skills in English.
  • Excellent interpersonal skills.
  • Advanced skills at team management, organization, and communication of priorities and listening
  • Practical experience in conducting and supporting CSV audits and inspections.
  • Advanced proficiency in the use of Microsoft Office desktop applications
REGULATORY KNOWLEDGE REQUIREMENTS
  • U.S. FDA Validation Guidance Document
  • 21 CFR Part 11 Electronic Records; Electronic Signature Final Rule
  • U.S. FDA Data Integrity Guidance
  • NIST Cybersecurity Framework
  • 21 CFR Part 210/211 cGMP
  • EUDRALEX Annex 11 Rules Governing Medicinal Products in the EU, Volume 4
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