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Contract Validation Engineer Jobs in Illinois (NOW HIRING)

Nemera

Quality Engineer - Validation

Buffalo Grove, IL · 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 ...

Nemera

Quality Engineer - Validation

Buffalo Grove, IL

$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 ...

Nemera

Quality Engineer - Validation

Buffalo Grove, IL · 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 ...

Staffingine LLC

Senior Java Full stack Developer

Chicago, IL · On-site

$59 - $75.25/hr

Collaborate on automated contract validation, drift detection, and compatibility checks. * Ensure ... You are a full stack software engineer, with 2-3 years of experience in engineering and development ...

Sterling Engineering Inc.

Sr. CQV Lead

Waukegan, IL

$65 - $75/hr

... Validation Engineer that has 5+ years of experience in pharma, biotech, API or specialty chemical manufacturing for a 6+ month onsite contract with strong potential for extension. This is not a ...

trane technologies

Project Engineer II

Willowbrook, IL · On-site

Coordinate with lead Validation Engineer to assess the impact on guaranteed savings of any changes to the contract scope of work. * Responsible for completing assigned tasks on time and within budget.

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How much do contract validation engineer jobs pay per hour?

As of Sep 5, 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.

Engineer, Validation Commissioning

AbbVie

North Chicago, IL • On-site

$65K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 25 days ago

AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 103 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
An engineering professional that works with project owners, automation engineers, subject designers/engineers and other project team members to plan, and complete tasks associated with commissioning, qualification and validation of new and modified automated systems equipment, facilities, utilities, product, processes etc.in line with project, operations and quality objectives. Level of responsibility and performance is commensurate with grade level. The primary objective is to design and execute robust evaluation, testing, and documentation strategies that support risk management, commissioning, and validation in alignment with product, regulatory, and quality requirements. The role also contributes to optimizing automated systems, process controls, and related technical workflows that support reliable and compliant manufacturing operations
Responsibilities
  • Work with end users, project engineers, and system owners to develop User Requirements Specifications and Functional/Design Specifications for new or modified facilities, utilities, and HVAC systems.
  • Support Factory Acceptance Testing and related verification activities to confirm facility and utility systems meet defined requirements prior to site deployment.
  • Identify risk controls, critical elements, and traceability of design requirements based on FMEA or other risk assessment approaches for qualified facilities and utility systems.
  • Develop and execute commissioning, qualification, and validation protocols for facilities, utilities, HVAC systems, and environmental/viable monitoring systems to ensure performance against specifications and intended use.
  • Perform minor troubleshooting of issues encountered during commissioning, including control logic, integration, instrumentation, documentation, and qualification deliverables.
  • May support project activities such as project leadership, development of operational procedures, training of maintenance/technical staff/operators on new equipment and utilities, reviewing new or modified documentation for compatibility with qualified systems, and implementing changes to equipment parameters or facility-related settings.
  • Support execution of risk management activities, including periodic review and update per the Validation Master Plan, interface with best practices and ccRA, and understanding of risk management principles, trace controls, change impact assessments, and rating scales. May perform FMEA authorization/facilitation as needed.
  • May serve as a QRM facilitator commensurate with responsibility.
  • Work with contract validation resources as part of a team to support timely completion of qualification activities within assigned area of responsibility.

Qualifications
  • Bachelor's Degree in Engineering, science, or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 1+ years of significant engineering and/or operational experience
  • Experience in the development of commissioning, qualification, validation or risk management deliverables including specifications and testing protocols that can stand up to regulatory scrutiny.
  • Experience with Computer System Validation (CSV) is required.
  • 2+ years of overall experience in Manufacturing, Quality or Engineering including 2 major validation subjects (e.g. Computer, Equipment, Cleaning, Process, etc.) preferred
  • Experience working with automation systems, controls, PLC/SCADA, instrumentation, or computer-based process controls strongly preferred.
  • A technical background in health care, nutritional products, laboratory diagnostics, medical devices, pharmaceutical, or similar industries (preferred).
  • Strong interpersonal, communication, and negotiation skills with demonstrated ability to work within a team environment.
  • Knowledge of quality / compliance management as well as regulations and standards affecting API, Bulk Drug or Finished goods manufacturing preferred
  • Works with junior or contract team members as part of a team
  • Ability to manage multiple projects (3+) simultaneously

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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