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Contract Validation Engineer Jobs in Illinois (NOW HIRING)

Validation Engineer

Ottawa, IL ยท On-site

$90K - $100K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Senior Validation Engineer Location: Ottawa, Illinois Employment Type: Full-Time About the Position ... Company Description About Us Fast growing liquid pour contract manufacturer of premium health and ...

An engineering professional that works with project owners, automation engineers, subject designers ... Work with contract validation resources as part of a team to support timely completion of ...

Engineer, Validation Commissioning

North Chicago, IL ยท On-site

$65K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

An engineering professional that works with project owners, automation engineers, subject designers ... Work with contract validation resources as part of a team to support timely completion of ...

Works with contract validation resources as part of a team in the timely completion of activities in his/her area of responsibility Qualifications * Bachelor's Degree in Engineering, science, or ...

Engineer, Validation Commissioning

North Chicago, IL ยท On-site

$65K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Works with contract validation resources as part of a team in the timely completion of activities in his/her area of responsibility Qualifications * Bachelor's Degree in Engineering, science, or ...

Works with contract validation resources as part of a team in the timely completion of activities in his/her area of responsibility Qualifications * Bachelor's Degree in Engineering, science, or ...

An engineering professional that works with project owners, automation engineers, subject designers ... Work with contract validation resources as part of a team to support timely completion of ...

Quality Engineer - Validation

Buffalo Grove, IL ยท On-site

$73K - $95K/yr

... and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany ... The Quality Validation Engineer is responsible for planning, coordinating and managing through ...

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Showing results 1-20

Contract Validation Engineer information

See Illinois salary details

$21

$50

$75

How much do contract validation engineer jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for contract validation engineer in Illinois is $50.39, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $61.25 per hour, depending on experience, location, and employer.

What are the primary responsibilities of a contract validation engineer on a typical project?

A Contract Validation Engineer is primarily responsible for reviewing and verifying that project deliverables, processes, and products comply with contractual requirements and industry standards. This includes conducting thorough documentation reviews, performing technical validations, and collaborating with project managers, legal teams, and quality assurance professionals to resolve any discrepancies. You will also support audits, maintain compliance records, and participate in meetings to ensure all stakeholders remain informed and aligned. The role often involves both independent analysis and teamwork, providing an excellent environment for those who enjoy balancing technical expertise with cross-functional collaboration.

What are the key skills and qualifications needed to thrive in the contract validation engineer position, and why are they important?

To thrive as a Contract Validation Engineer, you need strong analytical skills, a degree in engineering or a related field, and a deep understanding of contract requirements and industry regulations. Proficiency with validation software, quality management systems (QMS), and relevant certifications such as Six Sigma or ISO standards is often preferred. Outstanding attention to detail, effective communication, and the ability to work collaboratively across departments are crucial soft skills. These competencies ensure accurate contract assessments, regulatory compliance, and seamless integration of contractual obligations into engineering projects.

What is a contract validation engineer?

A Contract Validation Engineer is responsible for ensuring that systems, processes, and products meet regulatory and contractual requirements. They typically work on a temporary or project basis, verifying compliance through testing, documentation, and analysis. Their role involves collaborating with engineering teams to validate designs, troubleshoot issues, and ensure quality standards are met. This position is common in industries like pharmaceuticals, aerospace, and manufacturing, where strict validation protocols are required.

What are the most commonly searched types of Validation Engineer jobs in Illinois?

The most popular types of Validation Engineer jobs in Illinois are:

What job categories do people searching Contract Validation Engineer jobs in Illinois look for?

The top searched job categories for Contract Validation Engineer jobs in Illinois are:

Infographic showing various Contract Validation Engineer job openings in Illinois as of August 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 80% In-person, 10% Hybrid, and 10% Remote job distribution, with an average salary of $104,802 per year, or $50.4 per hour.

Validation Engineer

Sterling Engineering Inc.

Buffalo Grove, IL โ€ข On-site

$55 - $65/hr

Full-time

Re-posted 25 days ago


Job description

Validation Engineer – Injection Molding
Location: Buffalo Grove Il
Hire Type: Contract
Shift: 1st Shift | Monday–Friday
Compensation: $55–$65/hour
Overview
We are seeking a hands-on Validation Engineer with experience supporting plastic injection molding manufacturing within a regulated environment. This individual will lead equipment, process, and manufacturing validations while partnering closely with Manufacturing Engineering, Quality, Operations, and Automation teams to ensure new and existing molding processes meet quality and regulatory requirements.
The ideal candidate will have experience developing and executing IQ/OQ/PQ protocols, validating injection molding equipment and processes, troubleshooting manufacturing issues, and supporting continuous improvement initiatives in a medical device, pharmaceutical, or similarly regulated manufacturing environment.
Key Responsibilities
Develop, execute, and approve IQ, OQ, and PQ validation protocols for injection molding equipment, automation, and manufacturing processes.
Lead validation activities for new product introductions, equipment installations, process transfers, and manufacturing changes.
Validate injection molding processes including process windows, machine qualifications, tooling, auxiliary equipment, and automation systems.
Perform risk assessments utilizing FMEA and other risk management tools.
Investigate validation failures, process deviations, and nonconformances while implementing effective corrective actions.
Analyze process capability, statistical data, and validation results to ensure robust manufacturing processes.
Collaborate with Manufacturing Engineering to optimize molding parameters, cycle times, and process performance.
Support mold qualifications, process characterization, and production readiness activities.
Prepare validation reports, technical documentation, protocols, and supporting engineering documentation.
Participate in equipment FAT/SAT activities when applicable.
Ensure validation documentation complies with FDA, ISO 13485, GMP, and internal quality standards.
Support CAPA investigations, change control activities, and regulatory audits.
Work cross-functionally with Engineering, Quality, Production, Tooling, Automation, and Regulatory Affairs teams.

Qualifications

Bachelor's degree in Engineering or related technical discipline.
3+ years of validation engineering experience within a manufacturing environment.
Hands-on experience validating plastic injection molding processes and equipment.
Strong knowledge of IQ/OQ/PQ methodologies and validation lifecycle documentation.
Experience with process validation, equipment qualification, and manufacturing process development.
Familiarity with scientific molding principles and process optimization.
Experience with statistical analysis tools and process capability studies.
Knowledge of risk management methodologies including PFMEA/FMEA.
Strong technical writing and documentation skills.

Preferred Qualifications

Medical device, pharmaceutical, or highly regulated manufacturing experience.
Experience with automated manufacturing equipment, robotics, vision systems, and PLC-controlled equipment.
Knowledge of FDA 21 CFR Part 820, ISO 13485, GMP, and GAMP guidance.
Experience with injection mold qualification, tooling validation, and mold transfers.
Familiarity with cleanroom manufacturing environments.
Experience supporting CAPA, NCR investigations, and change control processes.
Working knowledge of Minitab or other statistical software.

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.