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Internship Medical Device System Engineer Jobs in Illinois

Collabera

Medical device engineer

North Chicago, IL

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

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

$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

$150 - $205/hr

Principal System Engineer 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 ...

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 ...

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Internship Medical Device System Engineer information

What is the difference between Internship Medical Device System Engineer vs Medical Device Quality Assurance Intern?

AspectInternship Medical Device System EngineerMedical Device Quality Assurance Intern
Required CredentialsTypically pursuing or holding a degree in engineering, biomedical, or related fieldsUsually enrolled in quality assurance, regulatory affairs, or related programs
Work EnvironmentDesign, develop, and test medical device systems in R&D or engineering teamsAssist in quality audits, documentation, and compliance activities in QA departments
Employer & Industry UsageUsed in medical device manufacturing companies, biotech firms, and R&D labsCommon in medical device manufacturing and regulatory compliance sectors

The Internship Medical Device System Engineer focuses on designing and testing device systems, while the Medical Device Quality Assurance Intern concentrates on ensuring product quality and compliance. Both roles are essential in the medical device industry but serve different functions during the product development and manufacturing process.

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:

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

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Cities in Illinois with the most Internship Medical Device System Engineer job openings:

Internship Medical Device System Engineer jobs near you

Medical Device Systems Engineer

North Chicago, IL

Sterling Engineering Inc.
See more jobs at Sterling Engineering Inc.external

$55 - $60/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 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.