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Internship Medical Device Consulting Jobs (NOW HIRING)

HealthTrust

AVP Medical Device Management

Lebanon, TN · On-site

The goals of SurgIntel analytics, medical device consulting, and physician engagement are to illustrate implant utilization, supply cost variation, deep clinical categorization, and price ...

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How much do internship medical device consulting jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for internship medical device consulting in the United States is $19.31, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.91 per hour, depending on experience, location, and employer.

What types of projects and responsibilities can I expect during an internship in medical device consulting?

As an intern in medical device consulting, you can expect to be involved in a range of projects, such as assisting with regulatory submissions, conducting market research, preparing technical documentation, and supporting client meetings. Many interns also help analyze data related to product safety, efficacy, and compliance with industry standards. You will likely work closely with experienced consultants, engineers, and regulatory specialists, gaining hands-on experience with real-world challenges faced by medical device companies. This collaborative environment offers valuable exposure to the consulting process and a chance to develop both technical and soft skills relevant to the medical device industry.

What are the key skills and qualifications needed to thrive as an Internship Medical Device Consulting, and why are they important?

To thrive as an intern in medical device consulting, you need a solid background in biomedical engineering, life sciences, or a related field, often supported by current enrollment in an undergraduate or graduate program. Familiarity with regulatory guidelines (such as FDA or ISO), data analysis tools, and project management software is highly beneficial. Strong analytical thinking, effective communication, and a collaborative mindset are standout soft skills in this role. These abilities ensure interns can contribute meaningfully to client projects, navigate complex compliance requirements, and support innovation within multidisciplinary teams.

What is an internship in medical device consulting?

An internship in medical device consulting is a temporary position where students or recent graduates gain hands-on experience working with consulting firms that specialize in advising medical device companies. Interns typically assist with projects related to regulatory compliance, product development, market analysis, and quality assurance. This role provides valuable exposure to the healthcare industry, helps interns develop problem-solving and communication skills, and can be a stepping stone to a career in medical device consulting or related fields.
What cities are hiring for Internship Medical Device Consulting jobs? Cities with the most Internship Medical Device Consulting job openings:
What are the most commonly searched types of Medical Device Consulting jobs? The most popular types of Medical Device Consulting jobs are:
What states have the most Internship Medical Device Consulting jobs? States with the most job openings for Internship Medical Device Consulting jobs include:
Internship Medical Device Consulting jobs near you
Medical Device/Combination Product Engineer

Medical Device/Combination Product Engineer

Ventura Solutions LLC

Vernon Hills, IL • On-site

$60K - $75K/yr

Full-time

Medical, Dental, Vision, PTO

Posted 26 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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