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Medical Device Testing Jobs in Chicago, IL (NOW HIRING)

Lead risk assessments to determine testing strategies. * Be involved in the medical device software design controls activities, in accordance with the FDA Quality System Regulation, ISO 13485, GAMP5 ...

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... testing, installation, and commissioning. Mechanical Automation Designer , Upchain , Upchain PLM , CAD workflows , 3D CAD , mechanical design , industrial automation , machine design , medical device ...

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Quality Inspector I

Lake Zurich, IL · On-site

$18 - $23/hr

Monday - Friday 6am - 2pm Employment Type: Full-Time About Us Founded in 1996, Medical Murray is a privately owned medical device company specializing in the development, testing, and manufacturing ...

Lead specialized security testing and threat modeling for FDA-regulated medical device software, ensuring compliance with HIPAA, GDPR, and FDA cybersecurity guidelines. * Develop high-quality ...

... other relevant medical device standards. ● Develop, implement, and maintain quality system ... testing, inspections, equipment qualification, and validation processes. ● Support the creation ...

... other relevant medical device standards. ● Develop, implement, and maintain quality system ... testing, inspections, equipment qualification, and validation processes. ● Support the creation ...

... other relevant medical device standards. ● Develop, implement, and maintain quality system ... testing, inspections, equipment qualification, and validation processes. ● Support the creation ...

... other relevant medical device standards. ● Develop, implement, and maintain quality system ... testing, inspections, equipment qualification, and validation processes. ● Support the creation ...

... other relevant medical device standards. ● Develop, implement, and maintain quality system ... testing, inspections, equipment qualification, and validation processes. ● Support the creation ...

R&D Senior Engineer

Barrington, IL · On-site

$95K - $160K/yr

Lake Zurich Employment Type: Full-Time About Us Founded in 1996, Medical Murray is a privately owned medical device company specializing in the development, testing, and manufacturing of finished ...

Showing results 41-60

Medical Device Testing information

See Chicago, IL salary details

$22

$37

$72

How much do medical device testing jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for medical device testing in Chicago, IL is $37.83, according to ZipRecruiter salary data. Most workers in this role earn between $25.53 and $47.31 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed for medical device testing?

To thrive in Medical Device Testing, you need a strong background in biomedical engineering, quality assurance, and regulatory compliance, often supported by a relevant degree. Hands-on experience with testing equipment, validation protocols, and familiarity with standards such as ISO 13485 and FDA guidelines are typically required. Attention to detail, analytical thinking, and clear documentation skills are essential soft skills for excelling in this field. These abilities ensure that devices meet safety and performance standards, protecting patient health and supporting company compliance.

What does medical device testing involve?

Professionals in Medical Device Testing typically spend their days conducting tests on new or existing medical devices to ensure they meet quality, safety, and regulatory standards. This often involves following strict protocols, documenting results accurately, and troubleshooting any performance or compliance issues that arise. Team members frequently collaborate with engineers, regulatory specialists, and manufacturing staff to ensure seamless product development and problem resolution. There may also be tasks related to preparing reports for regulatory submissions or participating in audits. This role offers the opportunity to make a real impact on patient safety while working in a collaborative, fast-paced environment.

What is medical device testing?

A Medical Device Testing job involves evaluating medical devices to ensure they meet regulatory standards, safety guidelines, and performance requirements. Professionals in this role conduct tests, analyze data, and document results to verify compliance with industry regulations such as FDA, ISO, and IEC standards. They work with engineers and regulatory teams to identify design flaws, improve product safety, and ensure reliability before market release. This job is crucial for preventing defects that could impact patient health and safety.

What are the most commonly searched types of Medical Device Testing jobs in Chicago, IL? The most popular types of Medical Device Testing jobs in Chicago, IL are:
What cities near Chicago, IL are hiring for Medical Device Testing jobs? Cities near Chicago, IL with the most Medical Device Testing job openings:
Infographic showing various Medical Device Testing job openings in Chicago, IL as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $78,687 per year, or $37.8 per hour.

Associate Research Scientist

Freseniusglobal

Lake Zurich, IL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Job description

Job SummaryThis Research Scientist performs studies supporting chemical characterization of materials to ensure safety and biocompatibility of materials for medical devices. Includes identification and quantitation of chemical compounds using advanced chemical instrumentation. Analytical method development and validation to support materials characterization of medical device components and solutions.
Salary Range: $85,000 - $100,000
Position is eligible to participate in a bonus plan with a target of 6% of the base salary
Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.
Applicants must be authorized to work for ANY employer in the United States. Fresenius Kabi is unable to sponsor or take over sponsorship of an employment visa either now or in the future.Responsibilities

Conduct drug container and medical device material evaluations studying the extractable/leachable compounds that can partition from device materials into fluids that are infused/transfused.
Conduct analysis of trace organic compounds for medical device materials using chromatography/mass spectrometry
Conduct elemental analysis for medical device materials for using ICP/MS
Independently generate study designs/protocols, write and distribute final reports.
Occasionally may work with samples that include human blood and blood components using procedural controls and personal protective equipment.
Assist the lab team in managing a laboratory testing capability that provides comprehensive chemical evaluation of materials for use in medical devices.
Assist the lab team supporting laboratory daily operations, calibrations and supplies.
Provide technical input/content for analytical method development and review.
Technical expert in the use and operation of ICP/MS and chromatography instrumentation with mass spectrometry detection.
Review laboratory documentation and results produced by colleagues.
Provide collegial support to fellow scientists.


This job position within the Business Unit - Transfusion and Cell Technologies (BU-TCT) of Fresenius Kabi USA hereby commits itself to protect any persons working under its control from work related hazards to health and safety as well as to protect the environment as the basis of life. This includes the prevention of diseases, incidents, and pollution as well as the responsible and sustainable use of resources. Our aim is to enhance our performance in the area of occupational and environmental safety, and to fulfill compliance obligations. To achieve this target, we implement and continuously improve the integrated management system according to ISO 14001 (Environmental Management System, or EMS) and ISO 45001 (Occupational Health and Safety Management Systems, or OHSMS).

Requirements

Requires working knowledge of laboratory analytical chemistry including classical techniques and advanced instrument systems.
Requires significant experience (5+ years) with the modern analytical tools and techniques of medical device and pharmaceutical product development. Must be experienced with with elemental analysis instrumentation including ICP/MS as well as gas chromatography (GC) and liquid chromatography (LC) equipped with mass spectrometry detectors.
Significant experience with (5+ years) laboratory instrumental techniques, method development, method validation. Experience with and instrument system validation desirable.
Must have solid experience with analytical mass spectrometry including use of advanced data processing systems.
A solid study director with total accountability for scientific study design, study execution, issue resolution and completion through audit.
Strong written and verbal communication skills in prior roles
Must have experience with FDA regulated laboratory environment of drug and medical device industries including GMP/GLP/GDP operations.
Must be able to routinely perform analytical laboratory testing while also demonstrating critical thinking including study design, interpretation of complex data sets, propose next steps for investigations based on newly acquired data. Must have adequate structural chemistry knowledge to facilitate interpretation of mass spectral data.
Bachelor's degree in chemistry is required. Advanced degree preferred. PhD in chemistry or a related discipline is preferred; alternatively, a Master's degree in Chemistry with specific and relevant experience in the areas defined under responsibilities and qualifications will be considered.

The Company's primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.

Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability,401K with company contribution, andwellness program.

Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is atwill, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.