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Internship Medical Device Software Engineer Jobs in Chicago, IL

Tempus

Senior Quality Engineer

Chicago, IL · On-site

As a Senior Quality Engineer , you will: * Lead verification, validation and maintenance of host ... Be involved in the medical device software design controls activities, in accordance with the FDA ...

Tempus

Senior Quality Engineer

Chicago, IL · On-site +1

As a Senior Quality Engineer , you will: * Lead verification, validation and maintenance of host ... Be involved in the medical device software design controls activities, in accordance with the FDA ...

Danaher

Software Engineer Internships

Aurora, IL

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Aurora, IL · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Gary, IN · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Chicago, IL · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Hammond, IN · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Collabera

Medical device engineer

North Chicago, IL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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

Tempus

Senior Application Security Engineer

Chicago, IL · On-site

$130K - $180K/yr

Lead specialized security testing and threat modeling for FDA-regulated medical device software ... engineering teams with hands-on remediation guidance. * Automate security testing by developing ...

Tempus

Senior Application Security Engineer

Chicago, IL

$130K - $180K/yr

Lead specialized security testing and threat modeling for FDA-regulated medical device software ... engineering teams with hands-on remediation guidance. * Automate security testing by developing ...

Tempus

Senior Application Security Engineer

Chicago, IL · On-site

$130K - $180K/yr

Lead specialized security testing and threat modeling for FDA-regulated medical device software ... engineering teams with hands-on remediation guidance. * Automate security testing by developing ...

Trudell Medical Group

Senior Software Engineer

Elgin, IL · On-site

$121K - $159K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

A minimum of 4 years of relevant work experience in the medical device field or other highly ... Fluent in C programming, Assembly and other software languages with ability to support migration to ...

STERIS Corporation

Advanced Software Engineer

Chicago, IL · Remote

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Advanced Software Engineer will work independently on complex technical problems, contribute to ... Experience working in healthcare, medical device, regulated, or quality-managed software ...

Steris Corporation

Advanced Software Engineer

Chicago, IL · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Advanced Software Engineer will work independently on complex technical problems, contribute to ... Experience working in healthcare, medical device, regulated, or quality-managed software ...

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Internship Medical Device Software Engineer information

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How much do internship medical device software engineer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for internship medical device software engineer in Chicago, IL is $26.18, according to ZipRecruiter salary data. Most workers in this role earn between $21.30 and $29.71 per hour, depending on experience, location, and employer.

What is an internship medical device software engineer?

An Internship Medical Device Software Engineer is a student or recent graduate who assists in designing, developing, and testing software used in medical devices under the supervision of experienced engineers. Their responsibilities may include coding, debugging, documentation, and ensuring that the software complies with healthcare regulations and standards. This internship provides hands-on experience in both software engineering and the unique requirements of the medical device industry, helping interns learn about safety, reliability, and regulatory compliance. Interns also collaborate with cross-functional teams, such as hardware engineers and quality assurance specialists, to contribute to the overall development process.

What does an internship medical device software engineer do?

As an internship medical device software engineer, you can expect to work on a variety of tasks such as writing and testing code for embedded systems, developing user interfaces, and assisting with software verification and validation processes. You may also help document code, participate in team meetings, and collaborate with senior engineers, quality assurance, and regulatory teams to ensure compliance with industry standards. This hands-on experience provides valuable exposure to the full product development lifecycle and offers opportunities to learn about the unique challenges of developing software for regulated medical devices.

What are the key skills and qualifications needed to thrive as an internship medical device software engineer?

To thrive as an Internship Medical Device Software Engineer, you need a foundational understanding of software development principles, programming languages like C/C++ or Python, and coursework in biomedical engineering or computer science. Familiarity with industry-specific tools such as version control systems (e.g., Git), embedded systems, and compliance standards like IEC 62304 is highly valued. Strong problem-solving abilities, attention to detail, and effective teamwork skills set top candidates apart. These competencies are essential to ensure the development of reliable, regulatory-compliant software that supports patient safety and innovation in medical technology.

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

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

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

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

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

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

What cities near Chicago, IL are hiring for Internship Medical Device Software Engineer jobs?

Cities near Chicago, IL with the most Internship Medical Device Software Engineer job openings:

Internship Medical Device Software Engineer jobs near you
Infographic showing various Internship Medical Device Software Engineer job openings in Chicago, IL as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $54,460 per year, or $26.2 per hour.

Senior Quality Engineer

Tempus

Chicago, IL • On-site

Full-time

Re-posted 14 days ago

Job description

Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
PLEASE NOTE: This is a hybrid role requiring three days a week in the office. Candidates can be based out of our Chicago (Headquarters), New York, or Redwood City locations.
As a Senior Quality Engineer, you will:
  • Lead verification, validation and maintenance of host systems supporting Tempus Medical Device(s).
  • 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, Computer System Validation (CSV) standards and FDA guidance, other applicable regulatory requirements, as well as best practices in the software industry.
  • Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and computer systems against user, functional and regulatory requirements.

Responsibilities:
  • Support regulatory compliance of the host system operating with Tempus Medical Device(s).
  • Develop and maintain CSV policies, procedures, templates and work instructions.
  • Lead risk-based approach to host / computer system validation (HSV/CSV), SDLC and design controls activities.
  • Perform validation, re-validation and change controls of various AI, SaaS, and Tempus in-house developed software.
  • Author and review software validation deliverables, including Risk Assessments, Validation Plans, Requirements (URS), Validation Protocols (IQ, OQ, PQ), UAT (User Acceptance Test), and Validation Reports.
  • Collaborate with cross-functional teams in developing test-driven system/functional requirements, defining testing strategies and participating in test execution.
  • Support Change Management and Major Incidents (MI) processes, ensuring organizational compliance and continuous improvement.
  • Provide support to Quality and IT organizations in maintaining compliance to various policies, procedures and activities, including support during internal/external inspections and regulatory and customer audits.
  • Provide CSV guidance, coaching, mentorship, and training to test engineers within the team.

Qualifications
  • BA/B.S. or higher preferred in Computer Science, Software Engineering, Informatics, Biomedical, or relevant engineering disciplines.
  • 5+ years experience in FDA regulated domain (e.g. medical device, pharma, biotech)
  • 3+ years experience in Computer System Validation (CSV).
  • Experience with industry standards and best practices for Medical device software and CSV such as Design Controls, GAMP 5, FDA 21 CFR Part 11, FDA (QSR) FDA 21 CFR 820.30, Medical device software (QMS) ISO 13485:2016, FDA 21 CFR 820, and Software life cycle processes (IEC 62304:2006).
  • Knowledge of quality system principles, practices, and standards for the life science industry.
  • Ability to deliver quality outputs without directions or under minimal supervision.

Chicago Pay Range: $90,000-$130,00
NYC/SF Pay Range: $100,000-$150,000
The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote roles- Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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