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Contract Validation Engineer Jobs in Illinois (NOW HIRING)

Sigan America LLC

Validation Engineer

Ottawa, IL · On-site

$90K - $100K/yr

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 ...

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How much do contract validation engineer jobs pay per hour?

As of Aug 28, 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 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 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 are the most commonly searched types of Validation Engineer jobs in Illinois?

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

What are popular job titles related to Contract Validation Engineer jobs in Illinois?

For Contract Validation Engineer jobs in Illinois, the most frequently searched job titles 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:

Contract Validation Engineer jobs near you
Infographic showing various Contract Validation Engineer job openings in Illinois as of August 2026, with employment types broken down into 88% Full Time, 9% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $104,802 per year, or $50.4 per hour.

Validation Engineer

Ottawa, IL • On-site

Sigan America LLC
Fitness and Sports Centers • 201 - 500 employees
Learn more about Sigan America LLCexternal

$90K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago

Job description

Senior Validation Engineer

Location: Ottawa, Illinois
Employment Type: Full-Time

About the Position

We are seeking an experienced Senior Validation Engineer to lead validation activities supporting our cGMP manufacturing operations. This role is responsible for validating equipment, facilities, utilities, manufacturing processes, and computerized systems while ensuring compliance with FDA cGMP requirements and industry best practices.

The ideal candidate has a strong technical background in pharmaceutical, medical device, cosmetic, or regulated manufacturing environments and enjoys working cross-functionally with Engineering, Quality, Manufacturing, Regulatory Affairs, Maintenance, and R&D.

Key Responsibilities

  • Develop, review, and execute IQ, OQ, and PQ validation protocols.
  • Plan and execute validation activities for new equipment, facilities, utilities, and manufacturing processes.
  • Support new product launches and continuous process improvement initiatives.
  • Prepare validation reports and maintain complete validation documentation.
  • Lead equipment qualification and process validation projects from planning through implementation.
  • Support engineering change controls and assess validation impact for equipment and process changes.
  • Perform periodic reviews and revalidation of equipment, utilities, and manufacturing processes.
  • Ensure compliance with FDA cGMP regulations, ISPE guidance, and internal quality standards.
  • Maintain validation records, equipment logbooks, and supporting documentation.
  • Collaborate with Maintenance, Engineering, Manufacturing, Quality Assurance, Regulatory Affairs, and R&D to resolve technical issues and implement improvements.
  • Identify opportunities to improve validation systems, documentation, and overall compliance.

Systems & Equipment Experience

Experience validating one or more of the following is highly desirable:

  • HVAC systems
  • Purified Water / RODI Water Systems
  • Compressed Air and Gas Systems
  • Boilers and Chillers
  • Temperature- and Humidity-Controlled Rooms
  • Refrigerators, Freezers, and Incubators
  • Manufacturing Equipment
  • Laboratory Equipment
  • Computerized Systems and 21 CFR Part 11 Compliance

Qualifications

Required

  • Bachelor's degree in Engineering, Life Sciences, or a related technical field (or equivalent experience).
  • 3–5+ years of validation experience in a pharmaceutical, medical device, cosmetic, or other FDA-regulated manufacturing environment.
  • Experience developing and executing IQ/OQ/PQ protocols.
  • Experience with equipment, facility, utility, and process validation.
  • Experience with engineering change controls and validation documentation.
  • Strong technical writing and documentation skills.
  • Excellent organizational skills with exceptional attention to detail.
  • Ability to manage multiple projects while meeting deadlines.

Preferred

  • Experience performing temperature mapping of refrigerators, freezers, incubators, warehouses, or controlled environments.
  • Experience with software validation and 21 CFR Part 11 compliance.
  • Experience completing validation periodic reviews.
  • Knowledge of risk-based validation methodologies.
  • Familiarity with Lean Manufacturing or Continuous Improvement initiatives.

What We're Looking For

The successful candidate is a hands-on validation professional who enjoys solving technical problems, improving manufacturing processes, and working collaboratively across departments. This individual is organized, detail-oriented, and committed to maintaining the highest standards of quality and regulatory compliance.

Competitive salary and comprehensive benefits package offered based on experience.

Company Description

About Us
Fast growing liquid pour contract manufacturer of premium health and beauty products.