ZipRecruiter

Log In

1

Medical Device System Engineer Jobs in Illinois (NOW HIRING)

Full Spectrum

Principal System Engineer

Lincolnshire, IL · On-site

$150K - $205K/yr

At Full Spectrum , our Systems Engineering team is the core differentiator that sets us apart from standard medical device service companies. As a Principal System Engineer ,you aren't just using a ...

Full Spectrum

Principal System Engineer

Lincolnshire, IL · On-site

$150K - $205K/yr

At Full Spectrum , our Systems Engineering team is the core differentiator that sets us apart from standard medical device service companies. As a Principal System Engineer , you aren't just using a ...

Full Spectrum

Principal System Engineer

Lincolnshire, IL · On-site

$150K - $205K/yr

At Full Spectrum , our Systems Engineering team is the core differentiator that sets us apart from standard medical device service companies. As a Principal System Engineer , you aren't just using a ...

Collabera

Medical device engineer

North Chicago, IL · On-site

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... Evaluate and integrate relevant engineering advances for improving or solving problems Understand ...

Intelas

Medical Device Integration Coordinator

Chicago, IL · On-site

$75K - $80K/yr

Supporting system upgrades, device replacements, operating-system migrations, planned maintenance ... Bachelor's degree in Information Technology, Computer Science, Biomedical Engineering, Healthcare ...

Duly Health and Care

RN Cardiac Device

Winfield, IL · On-site

$38.10 - $57.17/hr

EMR required, Epic and Paceart systems preferred * Interrogation and programming of Pacemakers ... medical issues and sometimes traumatic emotional events. The compensation for this role includes a ...

next page

Showing results 1-20

All JobsMedical Device System Engineer JobsMedical Device System Engineer Jobs in Illinois

Medical Device System Engineer information

See Illinois salary details

$51.8K

$123.3K

$161.8K

How much do medical device system engineer jobs pay per year?

As of Sep 2, 2026, the average yearly pay for medical device system engineer in Illinois is $123,274.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,000.00 and $152,100.00 per year, depending on experience, location, and employer.

What is a medical device system engineer?

A Medical Device System Engineer is responsible for designing, developing, and integrating complex medical device systems. They work across multiple engineering disciplines, including hardware, software, and regulatory compliance, to ensure that medical devices meet quality and safety standards. Their role involves risk analysis, system requirements definition, and verification and validation testing. They collaborate with cross-functional teams, including mechanical, electrical, and software engineers, as well as regulatory and clinical experts. Ultimately, they help bring safe and effective medical technologies to market.

What are typical daily tasks and responsibilities for a medical device system engineer?

Medical Device System Engineers are often responsible for designing, testing, and integrating complex medical devices while ensuring adherence to regulatory standards and safety requirements. Their daily tasks can include drafting system architectures, collaborating with electrical, mechanical, and software teams, conducting risk analyses, reviewing technical documentation, and supporting troubleshooting efforts during product development. They also frequently attend cross-functional meetings to align project timelines and discuss design improvements. This role provides a dynamic balance of hands-on engineering, project management, and regulatory compliance, making it ideal for individuals who enjoy challenging, mission-driven work in healthcare technology.

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

A Medical Device System Engineer requires a strong background in systems engineering, biomedical engineering, or a related field, along with expertise in medical device development and regulatory requirements. Familiarity with design tools (such as CAD and MATLAB), medical device quality standards (like ISO 13485), and risk management processes is highly valuable. Effective communication, problem-solving abilities, and teamwork distinguish candidates in collaborative, cross-disciplinary environments. These competencies are crucial for ensuring safe, innovative, and compliant medical devices that meet both user needs and regulatory expectations.

What are the most commonly searched types of Medical Device System Engineer jobs in Illinois?

The most popular types of Medical Device System Engineer jobs in Illinois are:

What are popular job titles related to Medical Device System Engineer jobs in Illinois?

For Medical Device System Engineer jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Medical Device System Engineer jobs in Illinois look for?

The top searched job categories for Medical Device System Engineer jobs in Illinois are:

Medical Device System Engineer jobs near you
Infographic showing various Medical Device System Engineer job openings in Illinois as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 50% In-person, and 50% Hybrid job distribution, with an average salary of $123,274 per year, or $59.3 per hour.

Medical Device Systems Engineer

Sterling Engineering Inc.

North Chicago, IL • On-site

$55 - $60/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago

Job description

Job Title: Medical Device Systems Engineer
Location: North Chicago, IL
Hire Type: Long-Term Contract (1+ year)
Target Pay Rate: $55.00 – $60.00/hour
Work Schedule: Onsite Monday-Friday
Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), & ESOP

Job Summary:
Seeking a Systems Engineer to support the development of innovative medical devices and therapeutic combination products within a highly regulated R&D environment. This role will primarily focus on Use-Related Risk Analysis (URRA) while also supporting broader systems engineering activities, including Design Inputs, Risk Management, Traceability, Systems Integration, and Design History File (DHF) architecture. The Systems Engineer will coordinate cross-functional risk assessments for drug delivery systems such as on-body devices, pre-filled syringes, autoinjectors, mixing devices, and electromechanical pumps, partnering closely with Human Factors, Quality, Clinical, Medical Safety, Development, and Manufacturing teams throughout clinical and commercial development.

Must Have Skills:
  • 3–5 years of experience in pharmaceutical, medical device, combination product, or another regulated industry.
  • Hands-on experience with Use-Related Risk Analysis (URRA), Human Factors, or Risk Management.
  • Strong experience with Design Controls and Design History File (DHF) documentation in a regulated environment.
  • Experience working in a cross-functional, matrixed organization with strong communication and facilitation skills.

Job Duties:
  • Lead and coordinate Use-Related Risk Analysis (URRA) activities across assigned medical device and combination product programs.
  • Facilitate cross-functional meetings and collaborate with Human Factors, Quality, Clinical, Medical Safety, Development, and Manufacturing teams to identify hazards, use errors, risks, and mitigations.
  • Support key systems engineering activities, including system architecture, user needs, product requirements, traceability, risk management, and change management.
  • Develop and maintain Design Control documentation and Design History Files (DHF) in accordance with applicable regulations and internal procedures.
  • Support risk assessments, including URRA, Design FMEA, and Process FMEA activities.
  • Monitor project schedules, milestones, risks, and deliverables; escalate issues and delays as needed.
  • Support integration of third-party development activities, including vendor communications and deliverable reviews.
  • Drive consistent execution of systems engineering and risk management processes and identify opportunities for improvement.

Qualifications:
  • BS in Engineering, Science, or a related technical discipline with 5+ years of relevant experience, or MS with 3+ years of experience.
  • 3–5 years of experience in pharmaceutical, medical device, combination product, or another regulated industry.
  • Experience with Use-Related Risk Analysis, Human Factors, Risk Management, and/or product development.
  • Strong experience with Design Controls and Design History File (DHF) management.
  • Working knowledge of systems engineering principles, including requirements definition, traceability, risk management, product architecture, and change management.
  • Experience with applicable regulatory standards such as FDA 21 CFR Part 820.30, 21 CFR Part 4, ISO 14971, ISO 13485, or EU MDR.
  • Strong organizational, facilitation, communication, and analytical skills.
  • Ability to influence cross-functional teams, manage competing priorities, and work effectively in a highly matrixed environment.
  • Experience with project tracking/document management tools and third-party vendor coordination preferred.
  • Experience supporting drug delivery systems, medical devices, or combination products preferred.


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.