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Internship Medical Device Testing Jobs in Ohio (NOW HIRING)

Senior Quality Engineer

Cincinnati, OH · On-site

$85K - $115K/yr

... testing and change control; drive continuous improvements. Requires Bachelor's in Biomedical Engineering or closely-related field & 3 yrs experience in medical device engineering position(s ...

Engineer III, Sustaining

Dublin, OH · On-site

$86K - $106K/yr

Coordinate technical assessments and testing associated with changes to resins, components ... Knowledge of medical device packaging systems, packaging validation, and accelerated aging ...

Design, maintain, and troubleshoot analog and digital circuits for a hospital-grade medical device * Own PCB development end-to-end: schematic design, layout, prototype bring-up, and testing * Power ...

Operator

Lewis Center, OH

$16.75 - $22/hr

Nelson Labs is a global leader in outsourced microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries. Sotera Health goes to market ...

Operator

Lewis Center, OH · On-site

$16.75 - $22/hr

Nelson Labs is a global leader in outsourced microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries. Sotera Health goes to market ...

... medical device industries. They are seeking a Junior Data Engineer to join their Information ... testing, release, and maintenance; • Communicate with team members regarding projects ...

Showing results 41-60

Internship Medical Device Testing information

What is an internship in medical device testing?

An internship in medical device testing is a temporary position where students or recent graduates gain hands-on experience working with medical devices to ensure their safety, effectiveness, and compliance with regulatory standards. Interns typically assist in performing laboratory tests, documenting results, and supporting engineers or quality assurance teams. This role helps interns understand industry protocols, testing methodologies, and regulatory requirements while developing practical skills for a future career in medical technology.

What types of projects and hands-on experiences can I expect during a medical device testing internship?

As a Medical Device Testing intern, you can expect to participate in a variety of projects that involve evaluating the safety, functionality, and reliability of medical devices. Typical responsibilities may include assisting with test setup, executing test protocols, recording and analyzing data, and collaborating with engineers and regulatory teams to ensure compliance with industry standards. Interns often gain exposure to specialized lab equipment, quality assurance practices, and regulatory documentation, all while working closely with experienced professionals in a team-oriented environment. This hands-on experience is valuable for building technical skills and understanding the product development lifecycle in the medical device industry.

What are the key skills and qualifications needed to thrive in a medical device testing internship?

To thrive in a Medical Device Testing internship, you need a solid background in biomedical engineering, life sciences, or a related field, often supported by coursework in device regulations and laboratory methods. Familiarity with testing equipment, data analysis software, and relevant standards like ISO 13485 or FDA regulations is typically expected. Strong attention to detail, effective communication, and problem-solving skills set standout candidates apart. These abilities ensure accurate testing, regulatory compliance, and clear reporting, which are critical for patient safety and product quality.

What is the difference between Internship Medical Device Testing vs Medical Device Quality Assurance Intern?

AspectInternship Medical Device TestingMedical Device Quality Assurance Intern
Required CredentialsTypically enrolled in related health sciences or engineering programsSimilar educational background, often in quality management or engineering
Work EnvironmentLaboratory and testing facilities, hands-on testing activitiesQuality management departments, documentation, and compliance tasks
Employer & Industry UsageManufacturers, testing labs, R&D departmentsManufacturers, regulatory agencies, compliance teams
Search & Comparison IntentUnderstanding testing roles in medical device developmentExploring quality assurance internship opportunities in medical devices

Internship Medical Device Testing focuses on hands-on testing and validation of medical devices, while Medical Device Quality Assurance Interns concentrate on ensuring compliance, documentation, and quality standards. Both roles are essential in the medical device industry and often overlap in skills and environment, but they serve different aspects of product development and regulation.

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

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

Senior Quality Engineer

Gentherm

Cincinnati, OH • On-site

$85K - $115K/yr

Full-time

Posted 20 days ago


Job description

Your Career. Your Impact. Your Future.  

At Gentherm, we believe the next big breakthrough begins with you. As a global leader in thermal management and pneumatic comfort technologies, we develop advanced systems that deliver meaningful solutions to enhance health, wellness, comfort, and efficiency in everyday life. Our products and innovations are created for you, by you. 

Be part of our team where a human-centric mindset drives everything we do-from the technologies we build to the careers we support. With decades of expertise, we have pioneered advanced solutions that have become a standard expectation for consumers around the world. 

The same thoughtful approach we take in developing our technologies guides how we support your career: purposeful, impactful, and tailored to you. Because when you thrive, innovation thrives. 

JOB TITLE

Senior Quality Engineer

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES

Senior Quality Engineer for Cincinnati, OH medical device manufacturer to maintain and improve Quality Management System to meet regulatory requirements; lead risk management activities; provide regulatory support during new product development; assist with CAPA & post-market surveillance activities; support verification & validation testing and change control; drive continuous improvements. Requires Bachelor's in Biomedical Engineering or closely-related field & 3 yrs experience in medical device engineering position(s): performing medical device design control during all phases of the product lifecycle, including creating & coordinating Design History Files (DHF), conducting design verification, and authoring design requirements; applying risk management methodologies, including FMEA & hazard analysis; ensuring product compliance with ISO 14971 & 13485 standards and U.S. and international medical device regulations, including EU MDR; and supporting Notified Body audits & FDA inspections, including performing document management & coordinating responses to observations and findings. Position may telecommute from location within reasonable commuting distance of Cincinnati, OH up to 1 day per wk. Mail resume to Gentherm Medical, LLC, Attn: A. Wylonis, 28875 Cabot Dr, Novi, MI 48377 or email resume to amanda.wylonis@gentherm.com Ref 573858

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MINIMUM QUALIFICATIONS
PREFERRED QUALIFICATIONS
NICE TO KNOW

Gentherm is an Equal Opportunity Employer. We are committed to building an inclusive culture through Our Network of Engagement (ONE) where we value our differences and work together to positively impact the lives of our employees, customers, and communities. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, genetic information, sexual orientation, gender identity, disability, or protected veteran status.