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Medical Device Internship Jobs in Ohio (NOW HIRING)

Abbott

2027 Finance Internship

Columbus, OH

$17.25 - $22.50/hr

Connect with us at abbott.com, on LinkedIn at and on Facebook at General Medical Devices Our ... device and management solutions for treating structural heart disease. EP In Abbott ...

Medpace

Junior Data Engineer

Cincinnati, OH · On-site

... medical device industries. They are seeking a Junior Data Engineer to join their Information ... field • Internship experience in Data or Software Engineering • Knowledge of developing ...

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All JobsMedical Device JobsMedical Device Internship JobsMedical Device Internship Jobs in Ohio

Medical Device Internship information

See Ohio salary details

$10

$18

$28

How much do medical device internship jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for medical device internship in Ohio is $18.36, according to ZipRecruiter salary data. Most workers in this role earn between $15.29 and $19.90 per hour, depending on experience, location, and employer.

What is a medical device internship?

A Medical Device Internship is a short-term position, typically for students or recent graduates, that provides hands-on experience in the medical device industry. Interns may work in various areas such as research and development, quality assurance, regulatory affairs, or engineering. The goal is to give participants practical exposure to how medical devices are designed, manufactured, tested, and brought to market while working alongside professionals in the field. This experience can help interns build valuable skills, network with industry experts, and improve their chances of securing a full-time role after graduation.

What types of projects and responsibilities can I expect during a medical device internship?

As a Medical Device Intern, you will typically be involved in a variety of hands-on projects that support product development, testing, or regulatory compliance. Interns often assist with tasks such as prototyping, data analysis, documentation for regulatory submissions, and collaborating with engineers or quality assurance teams. You may also participate in cross-functional meetings, learn about industry standards, and contribute to process improvements. This experience provides valuable exposure to both technical and regulatory aspects of the medical device industry, helping you build a strong foundation for a future career.

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 need a background in biomedical engineering or a related field, strong analytical skills, and a basic understanding of medical device regulations. Familiarity with CAD software, laboratory equipment, and regulatory standards such as FDA or ISO is often required. Strong communication, teamwork, and problem-solving abilities help interns contribute effectively to multidisciplinary projects. These skills ensure that interns can support innovation, comply with industry standards, and work efficiently within development teams.

What is the difference between Medical Device Internship vs Medical Device Technician?

AspectMedical Device InternshipMedical Device Technician
Required CredentialsTypically pursuing or recent graduate in biomedical, mechanical, or related fieldsPost-secondary certification or associate degree in biomedical technology or related field
Work EnvironmentOffice, laboratory, or manufacturing settings; focus on learning and trainingClinical, hospital, or repair facilities; hands-on device maintenance and troubleshooting
Employer & Industry UsageMedical device companies, hospitals, research institutions; internship programsMedical device manufacturing, healthcare facilities, repair services
Common Search & Comparison IntentEntry-level learning experience, career explorationTechnical repair, device maintenance, troubleshooting skills

The main difference between a Medical Device Internship and a Medical Device Technician is that internships are training roles for students or recent graduates focusing on learning about medical devices, while technicians are trained professionals responsible for maintaining, repairing, and troubleshooting medical devices in clinical or manufacturing settings.

What are the most commonly searched types of Medical Device jobs in Ohio?

The most popular types of Medical Device jobs in Ohio are:

What are popular job titles related to Medical Device Internship jobs in Ohio?

For Medical Device Internship jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Medical Device Internship jobs in Ohio look for?

The top searched job categories for Medical Device Internship jobs in Ohio are:

What cities in Ohio are hiring for Medical Device Internship jobs?

Cities in Ohio with the most Medical Device Internship job openings:

Medical Device Internship jobs near you
Infographic showing various Medical Device Internship job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 17% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $38,194 per year, or $18.4 per hour.

Device Engineer - GMP Manufacturing Support & Mechanical Testing (JP15754)

New Albany, OH

3 Key Consulting
Biotechnology Research and Development • 1 - 10 employees
Learn more about 3 Key Consultingexternal

$31 - $35/hr

Full-time

Posted 9 days ago

Job description

Job Title:   Device Engineer – GMP Manufacturing Support & Mechanical Testing (JP15754)
Location: New Albany, OH 43054
Employment Type: Contract
Business Unit: Commercial Drug Product
Duration: 1+ year (with likely extensions and/or conversion to permanent)
Posting Date: 08/20/2026
Pay Rate: $31 - $35/hour W2
Notes: Only qualified candidates need apply.  Fully Onsite (5 Days per Week) standard hours.  Potential overtime.
3 Key Consulting is hiring a  Device Engineer – GMP Manufacturing Support & Mechanical Testing for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Our ideal candidate:
  • Hands-on experience in engineering environments, particularly with tools like Instron systems and optical measurement methods
  • Proficiency in technical documentation and teamwork.
  • Hands-on experience working within a GMP manufacturing environment is required, including familiarity with GMP documentation practices, manufacturing operations, and quality systems.
  • Experience in regulated industries, preferably biopharma, biomedical, or medical devices, is strongly preferred, though aerospace or mechanical disciplines are acceptable provided the candidate also has relevant GMP manufacturing experience.
  • Proficiency in Microsoft Office is required, and CAD/SolidWorks skills are a plus.
  • Entry-level candidates with practical experience, such as internships within a GMP manufacturing or similarly regulated production environment, are preferred.

The Device Engineer will provide technical engineering support for material and component-related issues associated with commercial drug delivery devices and manufacturing operations. The primary focus of this role will be the triage, testing, investigation, escalation, and documentation of material-related issues identified during manufacturing or through other quality and technical support processes.
The engineer will work closely with Manufacturing, Quality, Engineering, and other cross-functional partners to assess reported issues, determine appropriate testing and investigation strategies, generate and review technical data, and support timely disposition or escalation of issues.
Scope includes mechanical delivery devices and associated components, including prefilled syringe systems. The qualified candidate will be part of a sustaining device engineering team supporting commercial manufacturing and product lifecycle activities. This position requires strong attention to detail, hands-on technical capabilities, and the ability to accurately document work within a GMP-regulated environment.
Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:
  • Strong Communication
  • Experience in a GMP Manufacturing Environment
  • Strong Technical Writing
  • Soft skills that need to be screened for: Looking for a self starter, someone who is ambitious

Day to Day Responsibilities:
  • Collaborate Cross-Functionally with the Various SMEs at the FDP Manufacturing Sites to Identify Device Issues and Root Causes
  • Expanding Documentation of Site Capability and Control Strategies
  • Ensuring Expedited communication to wider team on risks to device manufacturing
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Analyze and trend generated data by applying relevant statistical techniques to enable senior staff to make informed decisions
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Maintains combination product design history files for assigned products
  • Develops characterization test methods through fixture prototyping, reference sample creation, and GR&R analysis
  • Provides functional subject matter expertise to actively participate in cross-functional activities including system level root cause analysis, design changes, and change control assessments
  • Provide general laboratory support including inventory management, sample shipments, and cleanup.
  • Works with Scientists and Engineers, to assess and develop appropriate design and manufacturing specifications
  • Individual contributor with Leadership attributes to effectively represent device engineer within a large network/matrix organization

Basic Qualifications:
  • Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
  • At a minimum familiar with the following standards and regulations:
    • Quality System Regulation – 21CFR820
    • Risk Management – ISO 14971
    • EU Medical Device requirements – Council Directive 93/42/EEC
  • Demonstrates experience working in a GMP manufacturing environment and adheres to strict GMP documentation and compliance practices
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.

Preferred Qualifications:
  • Bachelor’s Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical, Bioengineering)
  • Minimum 2 years of scientific or engineering experience working in a GMP regulated manufacturing environment
  • Demonstrated understanding of GMP manufacturing operations, documentation practices, deviations/change controls, and working within an established quality system
  • Statistical Analysis software (Minitab or JMP)
  • Strong technical writing skills
  • CAD fixturing software (SolidWorks)
  • Tolerance Stack-Ups (2D, 3D, RSS)
  • Instron force tester using BlueHill Universal
  • CT-Scanning
  • Deviations and CAPAs
  • Experience with design controls; including (but not limited to) verification and design transfer
  • Understanding of risk assessments including hazard and probability analysis
  • Background in medical device development, commercialization and knowledge of manufacturing processes (fill-finish)
  • Ability to work independently and dynamically across functional teams
  • Excellent written and verbal communication skills
  • Ability to support complex workstreams under demanding timelines

Employee Value Proposition:
Unique industry opportunity, industry experience
Red Flags:
  • No Cross-Functional Experience
  • No Practical Work Experience

Interview process:
Initial 1:1 Phone Interview with Hiring Manager
Group Interview with CORE SMEs
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.