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Computer System Validation Manager Jobs in Lombard, IL

DSV A/S

System Specialist, WMS

Aurora, IL · On-site

Effectively communicates relevant IT-related information to site management and client management (as appropriate) * Maintains system efficiency. Will ensure the site's computer system allows all the ...

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 ... Computer Science or related * Preferred - Graduate Degree in Mathematics, Statistics, Economics ...

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 ... Computer Science or related * Preferred - Graduate Degree in Mathematics, Statistics, Economics ...

Pwc

Data Validation Risk - Manager

Chicago, IL

$99K - $232K/yr

Accounting, Engineering, Data Processing/Analytics/Science, Computer and Information Science ... Information Systems Auditor preferred - Demonstrating proficiency in data validation during ERP ...

Collabera

Validation Scientist

Glenview, IL

... in diverse food systems, which include proteins, carbohydrates and lipids. Qualifications ... manager. Keen problem solving skills and an investigative mind are needed. Must be able to work ...

Triton College, IL

Computer Technician

River Grove, IL · On-site

$17/hr

This includes projectors, screens, computer peripherals, control systems and video conferencing, as ... Must have valid Driver's License. * Must be able to lift 30-40 pounds unassisted. * Must be able to ...

ATLAS ENGINEERING GROUP

CAD MANAGER

Deerfield, IL · On-site

The CAD Manager will partner with civil and structural project managers, project engineers ... Knowledge of BIM processes and integration with CAD systems is a plus Computer Skills * Proficiency ...

Exelon

Trans System Operator I

Lombard, IL · On-site

Primary Purpose Operates the electric system, under the immediate supervision of the Shift Manager, Sr. Transmission System Operator and Transmission System Operator II, using various computer ...

Steve Madden

Store Assistant Manager

Aurora, IL

$15.75 - $21.25/hr

Process information or merchandise through the computer system and POS register system. Assist Store Manager in the selection and hiring of qualified candidates. Be flexible and occasionally perform ...

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All JobsComputer System Validation JobsComputer System Validation Manager JobsComputer System Validation Manager Jobs in Lombard, IL

Computer System Validation Manager information

See Lombard, IL salary details

$46.7K

$103.7K

$157.9K

How much do computer system validation manager jobs pay per year?

As of Aug 17, 2026, the average yearly pay for computer system validation manager in Lombard, IL is $103,737.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,300.00 and $129,900.00 per year, depending on experience, location, and employer.

What does a computer system validation manager do?

A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.

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

To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.

What are some common challenges a computer system validation manager faces during system implementation projects?

A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.

What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?

AspectComputer System Validation ManagerComputer System Validation Specialist
CertificationsGAMP, CQE, CSQEGAMP, CQE, CSQE
Work EnvironmentManagement, oversight, strategic planningExecution, testing, documentation
Industry UsagePharmaceutical, biotech, regulated industriesPharmaceutical, biotech, regulated industries
Primary FocusLeading validation projects, team coordinationPerforming validation activities, testing

The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.

What are popular job titles related to Computer System Validation Manager jobs in Lombard, IL?

For Computer System Validation Manager jobs in Lombard, IL, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Manager jobs in Lombard, IL look for?

The top searched job categories for Computer System Validation Manager jobs in Lombard, IL are:

What cities near Lombard, IL are hiring for Computer System Validation Manager jobs?

Cities near Lombard, IL with the most Computer System Validation Manager job openings:

Computer System Validation Manager jobs near you
Infographic showing various Computer System Validation Manager job openings in Lombard, IL as of June 2026, with employment types broken down into 94% Full Time, 4% Part Time, 1% Temporary, and 1% Contract. Highlights an 74% Physical, 2% Hybrid, and 24% Remote job distribution, with an average salary of $103,737 per year, or $49.9 per hour.

Validation Engineer

Sterling Engineering Inc.

Buffalo Grove, IL • On-site

$55 - $65/hr

Full-time

Re-posted 28 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.