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Validation Jobs in Chicago, IL (NOW HIRING)

Chemtech Plastics, Inc.

Validation Engineer

Elgin, IL

$85K/yr

Validation Engineer 1st shift E-Verify Location: Elgin, IL | On-Site Duties/Responsibilities: * Participate in projects/program management, review new and existing drawings as received from customers ...

Alliant Credit Union

Lead Model Validation

Chicago, IL · Hybrid

$95K - $163K/yr

Validate a broad range of models used across credit risk, treasury management (ALM), finance, underwriting, and related areas, includes both traditional statistical models and artificial intelligence ...

Alliant

Lead Model Validation

Chicago, IL · On-site

$95K - $163K/yr

Validate a broad range of models used across credit risk, treasury management (ALM), finance, underwriting, and related areas, includes both traditional statistical models and artificial intelligence ...

Synchrony Financial

AVP, Model Validation

Chicago, IL · On-site

The AVP, Model Validation is responsible for model validation and ensure they are meeting Model Risk Management policies, standards, procedures as well as regulations (OCC2011-12/SR 11-7). This role ...

Synchrony

AVP, Model Validation

Chicago, IL · On-site

The AVP, Model Validation is responsible for model validation and ensure they are meeting Model Risk Management policies, standards, procedures as well as regulations (OCC2011-12/SR 11-7). This role ...

Collabera

Validation Scientist

Glenview, IL

Company Description About Collabera: Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion ...

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All JobsValidation JobsValidation Jobs in Chicago, IL

Validation information

See Chicago, IL salary details

$23

$53

$80

How much do validation jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for validation in Chicago, IL is $53.56, according to ZipRecruiter salary data. Most workers in this role earn between $40.62 and $65.14 per hour, depending on experience, location, and employer.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

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 or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What is a validation job?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Chicago, IL? The most popular types of Validation jobs in Chicago, IL are:
Validation jobs near you
Infographic showing various Validation job openings in Chicago, IL as of August 2026, with employment types broken down into 88% Full Time, 5% Part Time, 1% Temporary, and 6% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $111,413 per year, or $53.6 per hour.

Validation Engineer

Sterling Engineering Inc.

Buffalo Grove, IL • On-site

$55 - $65/hr

Full-time

Re-posted 20 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.