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Validation Engineer Biomedical Jobs in Carol Stream, IL

IT EXCEL LLC

JR QA TESTER

Evanston, IL · On-site

$55K - $58K/yr

... IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA ... Qualifications Qualifications : BS in Biomedical Engineering/ BS in Chemical Engineering/ Computer ...

IT EXCEL LLC

JR QA TESTER

Evanston, IL

$55K - $58K/yr

... IN RESTON, VA Title: Jr. Validation Engineer/QA Analyst/ Jr. QA Tester/Business Analyst/BA ... Qualifications Qualifications : BS in Biomedical Engineering/ BS in Chemical Engineering/ Computer ...

Medline

Sr Engineer Design Electrical

Northfield, IL · On-site

$101K - $152K/yr

... validation builds, process development, and troubleshooting. * Support intellectual property ... Biomedical Engineering, or a related engineering discipline Work Experience * 4+ years of ...

Medline

Sr Engineer Design Electrical

Northfield, IL · On-site

$101K - $152K/yr

... validation builds, process development, and troubleshooting. * Support intellectual property ... Biomedical Engineering, or a related engineering discipline Work Experience * 4+ years of ...

Medline

Sr Engineer Design Electrical

Northfield, IL · On-site

$101K - $152K/yr

... manufacturing through validation builds, process development, and troubleshooting. Support ... Biomedical Engineering, or a related engineering discipline Work Experience 4+ years of experience ...

Medline

Sr Engineer Design Electrical

Northfield, IL · On-site

$101K - $152K/yr

... validation builds, process development, and troubleshooting. * Support intellectual property ... Biomedical Engineering, or a related engineering discipline Work Experience * 4+ years of ...

Medline

Sr Engineer Design

Northfield, IL · On-site

$101K - $152K/yr

... manufacturing through validation builds, process development, and troubleshooting. Support ... Education Bachelor's degree in mechanical engineering, biomedical engineering, electrical ...

Medline

Sr Engineer Design

Northfield, IL · On-site

$101K - $152K/yr

... validation builds, process development, and troubleshooting. * Support intellectual property ... Education * Bachelor's degree in mechanical engineering, biomedical engineering, electrical ...

Medline

Sr Engineer Design

Northfield, IL · On-site

$101K - $152K/yr

... validation builds, process development, and troubleshooting. * Support intellectual property ... Education * Bachelor's degree in mechanical engineering, biomedical engineering, electrical ...

Medline

Sr Engineer Design

Northfield, IL

$101K - $152K/yr

... validation builds, process development, and troubleshooting. * Support intellectual property ... Education * Bachelor's degree in mechanical engineering, biomedical engineering, electrical ...

Stryker Group

Staff Engineer - Sage, NPD

Cary, IL · On-site

$98 - $164/hr

Lead prototyping and testing efforts to validate design performance. * Identify and resolve complex ... Bachelor of Science in Engineering, Mechanical Engineering, or Biomedical Engineering. * Minimum ...

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Showing results 21-40

All JobsValidation Engineer Biomedical JobsValidation Engineer Biomedical Jobs in Carol Stream, IL

Validation Engineer Biomedical information

See Carol Stream, IL salary details

$23

$53

$80

How much do validation engineer biomedical jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for validation engineer biomedical in Carol Stream, IL is $53.78, according to ZipRecruiter salary data. Most workers in this role earn between $40.77 and $65.38 per hour, depending on experience, location, and employer.

What does a validation engineer do in biomedical?

A Validation Engineer in the biomedical industry ensures that equipment, processes, and systems used in the production of medical devices or pharmaceuticals meet regulatory standards and function as intended. Their work involves planning and executing validation protocols, documenting results, and troubleshooting any deviations. This role is crucial for maintaining product quality, patient safety, and compliance with regulatory agencies such as the FDA. Validation Engineers often collaborate with quality assurance, manufacturing, and research teams to establish and maintain validated systems throughout a product's lifecycle.

What are the key skills and qualifications needed to thrive as a validation engineer in biomedical?

To thrive as a Validation Engineer in Biomedical, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA or ISO 13485), and experience with validation protocols. Familiarity with technical tools like statistical analysis software, calibration equipment, and documentation systems is essential, and certifications such as Six Sigma or CQE can be advantageous. Strong problem-solving, attention to detail, and effective communication skills help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, meeting regulatory requirements, and ensuring patient safety in biomedical environments.

What are some typical challenges faced by validation engineers in the biomedical industry and how can they be addressed?

Validation Engineers in the biomedical field often face challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring equipment or processes meet stringent quality standards. Navigating audits and working cross-functionally with R&D, manufacturing, and quality assurance teams can also be demanding. To address these challenges, staying current with industry regulations, developing strong organizational and communication skills, and maintaining meticulous records are essential for success and career growth in this role.

What is the difference between Validation Engineer Biomedical vs Quality Assurance Engineer Biomedical?

AspectValidation Engineer BiomedicalQuality Assurance Engineer Biomedical
CertificationsGMP, ISO, FDA validation certificationsGMP, ISO, audit and compliance certifications
Work EnvironmentDesign, develop, and execute validation protocols for medical devicesDevelop and maintain quality systems, audits, and process improvements
Industry UsagePrimarily in medical device manufacturing and regulatory validationAcross medical device, pharmaceutical, and biotech industries

Validation Engineer Biomedical focuses on ensuring medical devices meet regulatory validation requirements through testing and protocols. Quality Assurance Engineer Biomedical emphasizes maintaining quality systems, compliance, and process improvements. Both roles are essential in the biomedical industry but serve different functions related to validation versus quality assurance.

What cities near Carol Stream, IL are hiring for Validation Engineer Biomedical jobs?

Cities near Carol Stream, IL with the most Validation Engineer Biomedical job openings:

Validation Engineer Biomedical jobs near you
Infographic showing various Validation Engineer Biomedical job openings in Carol Stream, IL as of August 2026, with employment types broken down into 77% Full Time, and 23% Contract. Highlights an 80% In-person, and 20% Hybrid job distribution, with an average salary of $111,862 per year, or $53.8 per hour.

Design Verification Engineer

Ventura Solutions LLC

Chicago, IL • On-site

$45 - $55/hr

Contractor

Medical, Dental, Retirement, PTO

Posted 29 days ago

Job description

Our client is seeking an experienced Design Verification Engineer to lead the planning, development, and execution of verification activities for medical device products. This individual will serve as a technical expert in device testing, design inputs, risk analyses, and translating product requirements into robust verification strategies and test methods.
The ideal candidate possesses a strong engineering background, understands how medical devices function from both a design and user perspective, and can independently determine what testing is required to demonstrate that design requirements have been met. This role works closely with R&D, Lab, Quality, Regulatory Affairs, and external partners throughout the product development lifecycle.
Responsibilities
  • Develop and execute design verification strategies for new and existing medical devices.
  • Review product requirements, design inputs, and risk analyses to determine appropriate verification activities.
  • Create verification protocols, test plans, acceptance criteria, and reports in compliance with applicable design control requirements.
  • Ensure objective evidence is generated to demonstrate compliance with design requirements.
  • Design, develop, optimize, and validate test methods for mechanical, functional, usability, environmental, reliability, and performance testing.
  • Identify and implement appropriate measurement systems, instrumentation, fixtures, and data acquisition methods.
  • Evaluate test method capability, repeatability, and reproducibility (e.g., GR&R).
  • Develop custom test equipment and fixtures as needed.
  • Support test method validation (TMV) and testing execution.
  • Analyze test data using statistical and engineering methods.
  • Support root cause analysis and recommend corrective actions.
  • Prepare clear technical reports and present findings to project teams and management.
  • Collaborate with Design Engineering, Quality, Regulatory Affairs, and Lab staff.
  • Coordinate testing activities with external laboratories, consultants, and suppliers.
  • Mentor junior engineers and provide leadership in verification and testing practices.
  • Support overall project planning from a testing strategy perspective.
  • Ensure verification activities comply with applicable standards, guidance documents, and internal procedures.
  • Participate in Design Control, Risk Management, and Design History File (DHF) activities.
  • Apply expertise in ISO 13485 and ISO 14971.

Qualifications
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Systems Engineering, or related discipline.
  • 5 years of experience in medical device development, verification, testing, or systems engineering.
  • Demonstrated experience developing verification strategies and executing design verification programs.
  • Strong understanding of medical device design controls and product development processes.
  • Experience developing test methods and analyzing data.
  • Excellent technical writing and communication skills.
  • Ability to independently assess designs and determine appropriate verification approaches.
  • Experience with inhalation, drug delivery, combination products, surgical, diagnostic, or other complex medical devices is a plus.
  • Knowledge of risk management and failure analysis methodologies is a plus.
  • Experience with statistical analysis tools such as Minitab, JMP, or equivalent is a plus.
  • Familiarity with IEC 60601, ISO 11608, or other applicable medical device standards is a plus.
  • Experience managing external test laboratories and contract development partners is a plus.

Location
  • Chicago, IL

Employee Type
  • W2 Contract (approximately 6 months)
  • Potential for contract-to-hire conversion

Compensation & Benefits
  • Hourly rate $45-$55
  • Medical and dental insurance
  • Paid vacation time
  • 401(k) after 90 days

About Ventura Solutions
Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com.
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