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Research Development Medical Device Engineer Jobs in Chicago, IL

Engineer II, DEV

Barrington, IL ยท On-site

$80K - $110K/yr

Title: R&D Engineer II Location: North Barrington Employment Type: Full Time About Us Founded in 1996, Medical Murray is a privately owned medical device company specializing in the development ...

R&D Senior Engineer

Barrington, IL ยท On-site

$95 - $160/hr

We partner with leading medical device companies to develop life-changing technologies that improve patient outcomes around the world. As a Senior R&D Engineer, you will play a critical leadership ...

... engineering required * Minimum of four years experience in quality systems management. * Minimum of four years experience in medical device development, manufacture and/or testing, with demonstrated ...

... engineering required * Minimum of four years experience in quality systems management. * Minimum of four years experience in medical device development, manufacture and/or testing, with demonstrated ...

Showing results 21-40

Research Development Medical Device Engineer information

See Chicago, IL salary details

$20.6K

$99.5K

$155.6K

How much do research development medical device engineer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for research development medical device engineer in Chicago, IL is $99,482.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,800.00 and $120,500.00 per year, depending on experience, location, and employer.

What are some typical challenges faced by research development medical device engineers when bringing a new device from concept to prototype?

Research Development Medical Device Engineers often encounter challenges such as navigating strict regulatory requirements, coordinating with cross-functional teams, and balancing innovation with manufacturability. Ensuring the device meets safety and efficacy standards while staying within budget and timeline constraints can be demanding. Additionally, effective collaboration with clinicians, quality assurance, and manufacturing teams is crucial to address technical hurdles and incorporate user feedback throughout the development process.

What does a research development medical device engineer do?

A Research Development Medical Device Engineer is responsible for designing, developing, and testing new medical devices or improving existing ones. They work closely with cross-functional teams, including clinicians, regulatory specialists, and manufacturing engineers, to ensure that devices are safe, effective, and compliant with industry standards. Their work involves prototyping, conducting experiments, analyzing data, and documenting results throughout the product development lifecycle. Additionally, they may help navigate regulatory approval processes and support product launches.

What is the difference between Research Development Medical Device Engineer vs Product Development Engineer?

AspectResearch Development Medical Device EngineerProduct Development Engineer
CredentialsBachelor's or Master's in Engineering, Biomedical, or related fields; certifications varyBachelor's or Master's in Engineering, Mechanical, Electrical, or related fields; certifications vary
Work EnvironmentResearch labs, R&D departments, clinical settingsManufacturing, design teams, product testing facilities
Employer & Industry UsageMedical device companies, biotech firms, healthcare institutionsMedical device companies, tech firms, manufacturing industries

The Research Development Medical Device Engineer focuses on early-stage research, innovation, and prototype development of medical devices. In contrast, the Product Development Engineer emphasizes designing, testing, and refining products for manufacturing and market release. Both roles require technical expertise, but their focus and project stages differ significantly.

What are the key skills and qualifications needed to thrive as a research development medical device engineer?

To thrive as a Research Development Medical Device Engineer, you need a strong background in biomedical engineering, mechanical or electrical engineering, and experience with product development processes, usually supported by a relevant degree. Familiarity with CAD software, prototyping tools, regulatory standards such as ISO 13485, and potentially Six Sigma or similar certifications is important. Creativity, analytical thinking, and effective teamwork skills help drive innovation and solve complex engineering challenges in multidisciplinary environments. These skills and qualifications are vital to ensure medical devices are safe, effective, and compliant with industry regulations while meeting user and market needs.
What job categories do people searching Research Development Medical Device Engineer jobs in Chicago, IL look for? The top searched job categories for Research Development Medical Device Engineer jobs in Chicago, IL are:
Infographic showing various Research Development Medical Device Engineer job openings in Chicago, IL as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $99,482 per year, or $47.8 per hour.

Engineer II, DEV

Medical Murray

Barrington, IL โ€ข On-site

$80K - $110K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 days ago


Job description

Title: R&D Engineer II

Location: North Barrington

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 devices, components, and subassemblies. We partner with clients ranging from innovative startups to the world’s largest OEMs. Our expertise includes permanent implants, delivery systems, and complex catheters for vascular, gastrointestinal, urologic, and other interventional markets.

Our culture is driven by five core values: Helpful, Happy, Personal Responsibility, Trustworthy and Clever & Skillful. These principles guide our work, our relationships, and our commitment to improving patient outcomes worldwide.


Benefits Summary

We offer a competitive compensation and benefits package, including medical (BCBS) and dental coverage, company-paid vision and life insurance, short- and long-term disability, HSA-eligible plans, a 401(k) Safe Harbor retirement plan, 18 days of PTO, TeleDoc access, identity protection, tuition reimbursement, voluntary life insurance, and paid time off for community volunteering.


Overview

At Medical Murray, innovation is at the heart of everything we do. We partner with leading medical device companies to develop groundbreaking technologies that improve patient care worldwide. As an R&D Engineer II, you will play a key role in designing and developing innovative medical devices while leading development projects from concept through production transfer.


This position is ideal for an engineer who enjoys hands-on product development, problem-solving, and collaborating with customers and cross-functional teams to bring new medical technologies to market. You'll have the opportunity to work on catheter-based and disposable medical devices while contributing to projects that directly impact patient outcomes.


What You'll Do

Product Design & Development

  • Develop and engineer disposable medical devices from concept through commercialization.
  • Design catheter-based delivery systems and other disposable medical devices using SolidWorks.
  • Build, evaluate, and refine prototypes in a laboratory environment.
  • Support product and process development activities for catheters and related disposable products.
  • Lead design modifications and improvements to existing product lines.

Project Leadership & Customer Support

  • Lead development projects while managing timelines, technical deliverables, and project objectives.
  • Communicate project status, risks, and technical updates to customers and internal stakeholders.
  • Support project planning activities including schedules, resources, and budgets.
  • Participate in project quotations and feasibility assessments.
  • Drive projects forward through development phases while meeting customer expectations.
  • Demonstrate leadership by sharing technical expertise and mentoring team members when appropriate.

Verification, Validation & Testing

  • Develop feasibility, reliability, verification, and validation testing plans.
  • Create and support in-vitro and in-vivo test methods and models.
  • Manage and support verification and validation activities, documentation, and reporting.
  • Assist with risk management activities including FMEA development and maintenance.
  • Analyze test data and provide recommendations to support design decisions.

Manufacturing & Process Development

  • Develop pilot and manufacturing equipment, processes, and procedures.
  • Assess manufacturing feasibility and support process validations and time studies.
  • Collaborate with Manufacturing Engineering to ensure successful technology transfer.
  • Support manufacturing operations until projects are fully transitioned into production.
  • Review manufacturing document changes for potential impact on design intent.

Equipment & Technical Support

  • Support acquisition, setup, installation, and qualification of new equipment.
  • Create preventive maintenance procedures as required.
  • Assist with equipment maintenance, troubleshooting, and escalation activities.
  • Support equipment requalification and return-to-service activities.
  • Collaborate with suppliers and vendors to source materials, components, and processing solutions.

Quality & Compliance

  • Follow all applicable Quality System requirements and Standard Operating Procedures.
  • Prepare and maintain design control documentation including project plans, design inputs, design outputs, test protocols, reports, risk analyses, and drawings.
  • Complete required project phase deliverables and documentation.
  • Support customer complaint investigations and resolution activities.
  • Ensure compliance with regulatory, customer, and internal quality requirements.


What You'll Bring

Education

  • Bachelor's or master’s degree in biomedical engineering, mechanical engineering, or related engineering discipline required.

Experience

  • 2–5 years of engineering experience within the medical device industry.
  • Experience with disposable medical device development preferred.
  • Experience with catheter-based products is highly desirable.
  • Experience leading technical projects and coordinating cross-functional activities.
  • Proficiency with SolidWorks or equivalent CAD software.

Technical Skills

  • Strong knowledge of product design and development processes.
  • Experience with materials selection, prototyping, and manufacturing processes.
  • Understanding of design controls, verification, validation, and risk management principles.
  • Familiarity with medical device development and commercialization activities.
  • Experience supporting process development and manufacturing transfer activities.

Skills & Competencies

  • Strong analytical and problem-solving abilities.
  • Excellent written, verbal, and interpersonal communication skills.
  • Ability to manage multiple projects and priorities in a fast-paced environment.
  • Strong organizational and project management skills.
  • Ability to work independently while collaborating effectively with customers, suppliers, and internal teams.
  • Proficiency with Microsoft Office applications and engineering software tools.

Why Join Medical Murray?

  • Work on innovative technologies that improve patient lives.
  • Partner with leading medical device companies and industry experts.
  • Gain exposure to a wide variety of products, technologies, and therapeutic areas.
  • Contribute directly to the development of life-changing medical devices.
  • Grow your technical and leadership skills in a collaborative, fast-paced environment.


Equal Opportunity Employer

Medical Murray is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.