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Internship R&D Engineer Medical Device Jobs in Michigan

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Support risk management activities (FMEA, hazard analysis) in accordance with ISO 14971 and Class II medical device design controls. * Help stand up engineering processes and documentation at the new ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Assemble medical devices and components according to engineering drawings, work instructions, and ... Prior experience in medical device assembly, electronics assembly, or precision manufacturing ...

KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... medical device, aerospace, or other high-technology manufacturing environments. * ASQ Certified ...

KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... medical device, aerospace, or other high-technology manufacturing environments. * ASQ Certified ...

KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... medical device, aerospace, or other high-technology manufacturing environments. * ASQ Certified ...

KLA focuses more than average on innovation and we invest 15% of sales back into R&D. Our expert ... medical device, aerospace, or other high-technology manufacturing environments. * ASQ Certified ...

ITT) is a diversified global leading manufacturer of highly engineered critical components and customized technology solutions serving the flow, aerospace and defense, transportation, industrial, and ...

R & D Test Technician

Novi, MI · On-site

$56K - $85K/yr

ITT) is a diversified global leading manufacturer of highly engineered critical components and customized technology solutions serving the flow, aerospace and defense, transportation, industrial, and ...

R & D Test Technician

Novi, MI · On-site

$56K - $85K/yr

ITT) is a diversified global leading manufacturer of highly engineered critical components and customized technology solutions serving the flow, aerospace and defense, transportation, industrial, and ...

R&D- Computer Vision Engineering Intern

Troy, MI · On-site

$16 - $20.50/hr

Knowledge of Python programming languages is expected. Additionally, knowledge of relevant mathematics, statistics, machine learning techniques, data pipelines, and software development workflows is ...

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Internship R D Engineer Medical Device information

What does an internship R&D engineer medical device do?

An Internship R&D Engineer in Medical Device assists in the research and development of new medical technologies and products. Their responsibilities typically include supporting senior engineers in designing, testing, and improving medical devices, conducting experiments, collecting and analyzing data, and preparing technical documentation. Interns also learn about regulatory standards and industry best practices while working as part of a multidisciplinary team. This role is ideal for students or recent graduates looking to gain hands-on experience in medical device innovation.

What types of projects or tasks can an internship R&D engineer medical device expect to work on?

As an Internship R&D Engineer in the medical device industry, you can expect to be involved in a variety of projects such as prototyping new device concepts, conducting laboratory experiments, performing data analysis, and supporting design verification and validation activities. Interns often collaborate closely with multidisciplinary teams, including senior engineers, regulatory specialists, and clinicians, to help solve real-world problems and improve patient outcomes. This hands-on experience provides valuable insight into the product development lifecycle and offers opportunities to contribute to meaningful projects that can enhance your technical and professional skills.

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

To thrive as an Internship R&D Engineer in Medical Devices, you generally need a background in biomedical engineering or a related field, with strong analytical and problem-solving abilities. Familiarity with CAD software, lab equipment, and basic knowledge of regulatory standards like ISO 13485 is important, and prior internships or relevant coursework can be advantageous. Attention to detail, effective communication, and collaborative teamwork skills help you contribute meaningfully to projects and navigate cross-functional environments. These skills ensure you can support innovative product development while adhering to strict safety and quality standards in the medical device industry.

What is the difference between Internship R&D Engineer Medical Device vs R&D Engineer Medical Device?

AspectInternship R&D Engineer Medical DeviceR&D Engineer Medical Device
QualificationsEnrolled in or recent graduate of engineering/biomedical programsBachelor's or Master's in engineering/biomedical fields
Work EnvironmentInternship programs, entry-level projects, supervised tasksFull-time, independent project work, team collaboration
ResponsibilitiesAssisting in research, testing, and documentationDesign, develop, and improve medical device products
Industry UsageCommonly used for training and entry-level experienceCore role in product development and innovation

In summary, the Internship R&D Engineer Medical Device is an entry-level position designed for students or recent graduates gaining initial industry experience. The R&D Engineer Medical Device is a full-time professional role with greater responsibilities in product development and innovation within the medical device industry.

What cities in Michigan are hiring for Internship R&D Engineer Medical Device jobs?

Cities in Michigan with the most Internship R&D Engineer Medical Device job openings:

Infographic showing various Internship R&D Engineer Medical Device job openings in Michigan as of August 2026, with employment types broken down into 50% Full Time, and 50% Nights. Highlights an 100% In-person job distribution.

Systems Engineer - Medical Device Company

Mitovation

Ann Arbor, MI • On-site

$110K - $140K/yr

Full-time

Medical

Posted 28 days ago

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Job description

About Mitovation

Mitovation is a clinical-stage medical device company developing a near-infrared photobiomodulation (NIR-PBM) therapy that protects the brain from reperfusion injury after cardiac arrest. The technology originated from mitochondrial biology research at Wayne State University and the University of Michigan and has progressed through an active FDA Investigational Device Exemption (IDE) and a pediatric clinical study. This position is funded through Mitovation's NIH Cooperative Agreement grant.

Position Summary

The Systems Engineer will be one of the first engineering hires at Mitovation, helping stand up a new company office in the Ann Arbor/Detroit, MI area. This role owns system-level architecture, integration, and verification across hardware, firmware, optics, and software subsystems, and works directly with Mitovation's external manufacturing partners to assist with the build of the clinical study systems used at trial sites.

Key Responsibilities

Clinical system support:

•      Own system-level builds and testing for the clinical study device platform, working with our manufacturing partner.

•      Support IDE maintenance and contribute engineering documentation supporting the clinical study.

New system design / development:

•      Translate clinical and user needs into system, subsystem, and component-level technical requirements, and maintain traceability through the design history file.

•      Lead system integration across electrical, mechanical, optical, firmware, and software subsystems, coordinating with the manufacturing partner throughout the build process.

•      Develop and execute verification and validation (V&V) test protocols; author associated technical reports.

•      Support risk management activities (FMEA, hazard analysis) in accordance with ISO 14971 and Class II medical device design controls.

•      Help stand up engineering processes and documentation at the new company office as an early technical hire.

•      Support buildout of a Quality Management System (QMS) in anticipation of future ISO 13485 certification.

Required Qualifications

•      Bachelor's degree in Biomedical, Electrical, Mechanical, or Systems Engineering (or related field); advanced degree a plus.

•      5+ years of systems engineering experience in medical devices, with direct experience in design controls (21 CFR 820.30 / ISO 13485).

•      Demonstrated experience taking a device from prototype/early clinical stage through design V&V.

•      Working knowledge of risk management standards (ISO 14971) and IEC 60601 electrical safety requirements for medical electrical equipment.

•      Comfort working in a small-company, early-stage environment — willing to be hands-on with builds and testing as well as documentation and process.

•      Strong cross-functional communication skills; able to work directly with founders, clinical partners, and the external manufacturing partner.

Preferred Qualifications

•      Experience with optical or light-based therapeutic devices (photobiomodulation, phototherapy, laser/LED systems).

•      Experience working alongside a contract manufacturer or external build partner on clinical or early-production device units.

•      Familiarity with FDA IDE and De Novo/510(k) regulatory pathways.

What Mitovation Offers

•      The opportunity to build the engineering foundation of a company developing a first-in-category neuroprotection therapy, with FDA IDE already in hand and an active clinical study underway.

•      A seat at the table during a pivotal growth phase — this hire directly shapes the technical team and the new company office.

•      Competitive salary and benefits, commensurate with an early-stage medical device company.

Company Description

Mitovation is a Michigan based medical device startup company with their first product treating post cardiac arrest re-perfusion injury.
Why is this a breakthrough? Cardiac arrest impairs systemic perfusion and renders the brain and other organs ischemic. The brain is highly reliant on a constant supply of oxygen and nutrients and thus is particularly sensitive to the resultant deficit in blood flow. In the absence of rapid resuscitation and restoration of blood flow, ischemia leads to severe neurologic damage. While resuscitation is required to preserve neurologic function, it also initiates re-perfusion injury, which plays a major role in the compromised recovery of resuscitated patients, and is thought to contribute significantly to the high incidence of morbidity and mortality associated with cardiac arrest. Despite advances in cardiopulmonary resuscitation, neurological function – a primary metric for clinical outcome – remains poor following cardiac arrest and resuscitation.

Mitovation has developed a breakthrough technology to prevent the brain damage that occurs from a cardiac arrest.