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Full Time Medical Device Engineer Jobs in Chicago, IL

Intelas

Medical Device Integration Coordinator

Chicago, IL · On-site

$75K - $80K/yr

Bachelor's degree in Information Technology, Computer Science, Biomedical Engineering, Healthcare Technology Management, or a related field. * Experience with Epic, HL7, medical-device integration ...

Ventura Solutions LLC

Sales Engineer

Barrington, IL · On-site +1

We are seeking a dynamic and results-driven Medical Device Sales Engineer to drive the growth of ... Location * Lake Barrington, IL or Remote for the right candidate Employment Type * Full-time ...

Ventura Solutions LLC

Sales Engineer

Barrington, IL · On-site

We are seeking a dynamic and results-driven Medical Device Sales Engineer to drive the growth of ... Location * Lake Barrington, IL or Remote for the right candidate Employment Type * Full-time ...

Del Medical, Inc.

Assembler

Bloomingdale, IL · On-site

$19 - $22/hr

Del Medical, Inc. is a leading company in the medical device manufacturing industry. We're looking ... Read and understand Engineering Blueprints and instructions to put together medical products ...

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All JobsMedical Device Engineer JobsFull Time Medical Device Engineer JobsFull Time Medical Device Engineer Jobs in Chicago, IL

Full Time Medical Device Engineer information

See Chicago, IL salary details

$22

$51

$99

How much do full time medical device engineer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for full time medical device engineer in Chicago, IL is $51.34, according to ZipRecruiter salary data. Most workers in this role earn between $36.15 and $61.39 per hour, depending on experience, location, and employer.

What is the difference between Full Time Medical Device Engineer vs Medical Device Quality Engineer?

AspectFull Time Medical Device EngineerMedical Device Quality Engineer
Required CredentialsBachelor's in Engineering, certifications like CQA or Six Sigma beneficialBachelor's in Engineering or Life Sciences, certifications like CQE or ISO auditor
Work EnvironmentDesign labs, R&D departments, manufacturing facilitiesQuality assurance labs, compliance departments, manufacturing sites
Employer & Industry UsageMedical device companies, biotech firms, healthcare device manufacturersMedical device companies, regulatory agencies, compliance firms
Common Search & ComparisonYesYes

Full Time Medical Device Engineers focus on designing, developing, and testing medical devices, working closely with R&D teams. Medical Device Quality Engineers concentrate on ensuring products meet quality standards and regulatory requirements. Both roles are essential in the medical device industry but differ in their primary responsibilities and work environments.

What are the most commonly searched types of Medical Device Engineer jobs in Chicago, IL?

The most popular types of Medical Device Engineer jobs in Chicago, IL are:

What are popular job titles related to Full Time Medical Device Engineer jobs in Chicago, IL?

For Full Time Medical Device Engineer jobs in Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Full Time Medical Device Engineer jobs in Chicago, IL look for?

The top searched job categories for Full Time Medical Device Engineer jobs in Chicago, IL are:

Full Time Medical Device Engineer jobs near you
Infographic showing various Full Time Medical Device Engineer job openings in Chicago, IL as of August 2026, with employment types broken down into 100% Full Time. Highlights an 94% In-person, 2% Hybrid, and 4% Remote job distribution, with an average salary of $106,787 per year, or $51.3 per hour.

Medical Device Systems Engineer

Sterling Engineering Inc.

North Chicago, IL

$55 - $60/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago

Key responsibilities

  • 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.

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.