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Computer 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 ... Prolonged periods sitting at a desk and working on a computer. * Office environment. * Must be able ...

Frontage Laboratories

QA Specialist/Auditor

Chicago, IL · On-site

$65K - $75K/yr

Serve on various internal committees (e.g., computer validation, SOP review, etc.) to provide a QA perspective on the issues discussed. E ducation, Experience & Skills Required: * Must have a minimum ...

Ankura

Model Validation Director

Chicago, IL · On-site +1

The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...

Triton College, IL

Computer Technician

River Grove, IL · On-site

$17/hr

Must have valid Driver's License. * Must be able to lift 30-40 pounds unassisted. * Must be able to ... Maintain records/inventory related to computer equipment (PC/ iMAC's) including procuring the use ...

Hartford Technology Rental

Be Seen First

Computer Technician

Arlington Heights, IL · On-site

$20/hr

Computer Equipment - Arlington Heights, IL Are you looking for great pay & benefits, training, and ... Valid driver's license * Ability to lift fifty pounds Preferred Qualifications: * Basic knowledge ...

ABOC

Computer Operator

Chicago, IL · On-site

$21/hr

This position is responsible for accurately and efficiently performing transaction capture, data entry, data validation, computer equipment and communication. RESPONSIBILITIES: * Transmits customer ...

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All JobsComputer Validation JobsComputer Validation Jobs in Chicago, IL

Computer Validation information

See Chicago, IL salary details

$10

$55

$88

How much do computer validation jobs pay per hour?

As of Jun 27, 2026, the average hourly pay for computer validation in Chicago, IL is $55.96, according to ZipRecruiter salary data. Most workers in this role earn between $43.08 and $66.35 per hour, depending on experience, location, and employer.

Can computer engineers make $500,000?

Computer validation professionals typically do not earn $500,000 annually, as this level of compensation is uncommon in the field. High salaries may be possible for senior roles, especially in biotech or pharmaceutical industries, or with extensive experience, specialized skills, and leadership responsibilities. Most salaries for computer validation roles range from $70,000 to $150,000 per year.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What is the salary of a CSV engineer?

A CSV (Computer System Validation) engineer's salary typically ranges from $70,000 to $120,000 annually, depending on experience, location, and certifications. Senior roles or those with specialized skills in validation tools and regulatory compliance may earn higher salaries.

Is computer system validation a good field?

Computer validation professionals ensure that computer systems in regulated industries meet quality and compliance standards, often working with tools like GxP and validation protocols. The field offers steady demand, especially in pharmaceuticals and biotech, and requires knowledge of regulatory requirements and validation processes. It can be a rewarding career for those interested in quality assurance, compliance, and technical problem-solving.

Is CSV a skill?

In the context of computer validation, familiarity with CSV (comma-separated values) files is considered a useful technical skill, as it involves working with data formats and data management tools. Proficiency in handling CSV files can support tasks such as data import/export, validation, and reporting. However, CSV itself is a data format, not a standalone skill, but understanding how to work with it is valuable for validation professionals.
What are popular job titles related to Computer Validation jobs in Chicago, IL? For Computer Validation jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in Chicago, IL look for? The top searched job categories for Computer Validation jobs in Chicago, IL are:
Computer Validation jobs near you
Infographic showing various Computer Validation job openings in Chicago, IL as of June 2026, with employment types broken down into 80% Full Time, 5% Part Time, and 15% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $116,389 per year, or $56 per hour.
Validation Engineer

Validation Engineer

Chemtech Plastics, Inc.

Elgin, IL

$85K/yr

Full-time

Medical, Dental, Vision

Posted 13 days ago

Job description

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 and evaluate potential quality issues.
  • Develop and execute IQ, OQ, and PQ validation protocols for production processes, equipment and software in a timely and cost-effective manner.
  • Write reports summarizing results for equipment, process or software validation projects.
  • Determine deliverables with the customer and cost estimate the sampling requirements and inspection activity.
  • Review existing validation reports and identify/mitigate gaps for compliance to requirements
  • Work with Q.A. Dept. on piece part inspections and capability studies of new mold and engineering changes to ensure all requirements are completed and approved.
  • Conduct or lead corrective and preventive actions in quality systems or validations using problem solving techniques.
  • Participate as an active new product development core team member.
  • Process all stages of validation documents and oversee the completion and signatures.
  • Support quality system projects and activities such as engineering change order support and complaint investigation support.
  • Support FDA inspection readiness activities.
  • Interfacing customers, staff and fellow managers to establish and maintain validation schedules throughout the company.
  • Ability to interact with customers in all necessary situations to keep them informed of progress and documentation status.
  • Consults with customers on quality and inspection-related issues.
  • Manages and holds project meetings with customers.
  • Other duties as assigned by the Director of Engineering.
Required Skills/Abilities:
  • Excellent written and verbal communication skills and highly effective time management skills.
  • Ability to operate independently and as part of a team
  • Independent problem-solving skills
  • Proficient in root cause analysis, verification amp; validation, process flow mapping
  • Technical and procedural understanding of customer requirements for part validation.
  • Project management skills include planning, processing, organizing and tracking of all part validation activities.
  • Experience processing data in MiniTab software and correlate P values.
  • Knowledge of processes and procedures for cost estimating of validation work.
Education and Experience:
  • Bachelor of Science degree from an accredited college or university in an Engineering or Science discipline and 3-5 years of process/software validation experience in a regulated industry
  • Working knowledge of Medical Device Regulations and Standards (FDA, ISO 13485, ISO 14971, MDD, IVDD)
Physical Requirements:
  • Prolonged periods sitting at a desk and working on a computer.
  • Office environment.
  • Must be able to lift 15 lbs.
  • Must be able to access and navigate each department at the organization’s facilities.
Benefits and Compensation:
  • Full benefit offerings including medical, dental, vision, and voluntary plans
  • $85,000 annually

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