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Internship Medical Device Intern Jobs in Illinois

Sotera Health

Marketing Sales Intern

Oak Brook, IL · On-site

... 50 medical device companies and 9 of the top 10 pharmaceutical companies. The Marketing & Sales ... The intern will collaborate closely with cross-functional teams to help drive customer engagement ...

Danaher

Software Engineer Internships

Rockford, 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

Chicago, 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

Joliet, 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

Dekalb, 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

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

Peoria, 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 ...

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Internship Medical Device Intern information

What are the key skills and qualifications needed to thrive as a Medical Device Intern, and why are they important?

To thrive as a Medical Device Intern, you typically need a background in biomedical engineering, life sciences, or a related field, along with solid analytical and problem-solving skills. Familiarity with CAD software, laboratory equipment, and quality management systems, as well as knowledge of relevant regulatory standards, is often required. Strong teamwork, adaptability, and effective communication are essential soft skills for collaborating on cross-functional projects and presenting findings. These competencies ensure interns can contribute meaningfully to device development, comply with industry standards, and support innovation in a regulated environment.

What types of projects and responsibilities can I expect as a Medical Device Intern?

As a Medical Device Intern, you can expect to support ongoing projects in areas such as product development, testing, quality assurance, or regulatory affairs. Typical responsibilities may include assisting with laboratory experiments, documenting results, preparing technical reports, and collaborating with cross-functional teams like engineering, clinical, or manufacturing. Interns often gain exposure to the medical device lifecycle and learn about regulatory standards, making this role an excellent opportunity for hands-on learning and professional growth. You'll also have the chance to participate in team meetings and contribute ideas to improve product safety and effectiveness.

What does a Medical Device Intern do?

A Medical Device Intern typically assists in the development, testing, and documentation of medical devices under the supervision of experienced engineers or scientists. Their responsibilities may include conducting research, supporting design and prototyping, running laboratory tests, collecting and analyzing data, and ensuring compliance with regulatory standards. The internship provides hands-on experience and exposure to the medical device industry, helping students or recent graduates gain valuable skills and knowledge in the field.
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What cities in Illinois are hiring for Internship Medical Device Intern jobs? Cities in Illinois with the most Internship Medical Device Intern job openings:
Internship Medical Device Intern jobs near you
Infographic showing various Internship Medical Device Intern job openings in Illinois as of May 2026, with employment types broken down into 19% Internship, 51% Full Time, 22% Part Time, 4% Temporary, and 4% Contract. Highlights an 92% In-person, 4% Hybrid, and 4% Remote job distribution.
Medical Device/Combination Product Engineer

Medical Device/Combination Product Engineer

Ventura Solutions LLC

Vernon Hills, IL • On-site, Remote

$60K - $75K/yr

Other

Medical, Dental, Vision, PTO

Posted 27 days ago

Job description

We are seeking passionate and driven Medical Device/Combination Product Engineers to join our medical device consulting team. This is an ideal opportunity for recent graduates or those with limited experience who are excited to apply their academic knowledge in real-world product development.

If you have a strong interest in medical devices, pharmaceuticals, and combination products, and are eager to gain hands-on experience in product development, design controls, and risk management, we want to meet you!

As a Medical Device/Combination Product Engineer, you will support the development and maintenance of medical devices and combination products by assisting with technical documentation, testing, and cross-functional collaboration. You’ll contribute to the creation of Design History Files (DHF), risk management files, and other engineering documentation in accordance with industry regulations and standards such as FDA 21 CFR 820 and ISO 14971.

Responsibilities

  • Assist in developing and maintaining Design History Files (DHF) and Risk Management Files for medical devices and combination products
  • Support product development activities, including gathering user needs, design inputs, and testing requirements
  • Participate in risk assessment activities, such as creating or supporting FMEAs
  • Help prepare and review technical documentation for design verification and validation
  • Research applicable regulations, standards, and guidance documents to support compliance efforts
  • Work closely with cross-functional teams, including Quality, Regulatory, Manufacturing, Human Factors, and Clinical
  • Contribute to design control activities and help ensure traceability from requirements through testing
  • Support documentation for inspections and regulatory submissions

Qualifications

  • Bachelor’s degree in Biomedical Engineering or related engineering discipline (e.g., Mechanical, Chemical, Electrical)
  • Strong academic foundation in engineering principles and a desire to apply them in a regulated industry
  • Understanding of or exposure to design control, risk management, and product development lifecycle through coursework, internships, or academic projects
  • Strong written and verbal communication skills
  • Detail-oriented with good documentation and organizational skills
  • Team-oriented with a willingness to learn and grow in a fast-paced environment

Preferred (Not Required) Experience

  • Internship, co-op, or project work related to medical devices, drug delivery, or combination products
  • Familiarity with standards like ISO 13485, ISO 14971, or FDA design control regulations
  • Exposure to tools such as FMEA, DHF documentation, or verification test planning
  • Experience with engineering software (CAD, Minitab, MATLAB, etc.)

Location

  • Northwest Chicago Suburbs or remote for the right candidate

Employee Type

  • W2 Employee

Compensation and Benefits

  • Salary: $60,000 - $75,000 annually, depending on experience
  • Choice of medical, dental, and vision plans
  • Paid Vacation Time
  • Competitive base salary

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com.

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