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Entry Level Medical Device Jobs in Ohio (NOW HIRING)

Stereotaxis

Territory Assistant

Cleveland, OH · On-site

$18.25 - $23.75/hr

... Entry Level Category Account Management Date Needed By Job Type Full-time Travel Company ... This is an opportunity to enter medical device sales at base level and develop skills to advance in ...

Medpace, Inc.

Entry Level Recruiter

Cincinnati, OH · On-site +1

$34K - $45K/yr

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device ...

Medpace, Inc.

Entry Level Recruiter

Cincinnati, OH · On-site

$34K - $45K/yr

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device ...

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All JobsMedical Device JobsEntry Level Medical Device JobsEntry Level Medical Device Jobs in Ohio

Entry Level Medical Device information

See Ohio salary details

$9

$19

$42

How much do entry level medical device jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for entry level medical device in Ohio is $19.89, according to ZipRecruiter salary data. Most workers in this role earn between $13.84 and $21.53 per hour, depending on experience, location, and employer.

What is an entry level medical device job?

Entry level medical device jobs are positions within medical device companies that are designed for individuals who are new to the industry or just starting their careers. These roles can include positions such as sales representatives, quality assurance associates, regulatory affairs assistants, and manufacturing technicians. They typically require a bachelor's degree in a related field, strong communication skills, and a willingness to learn. Entry level employees may assist with product launches, support senior staff, and ensure products meet regulatory standards. These roles offer valuable experience and a pathway to more advanced positions within the medical device industry.

What are the key skills and qualifications needed to thrive as an entry level medical device sales representative?

To thrive as an Entry Level Medical Device Sales Representative, you need a bachelor’s degree (often in life sciences, business, or a related field), strong sales acumen, and a good understanding of medical terminology. Familiarity with CRM systems, sales tracking software, and product-specific training or certifications like the Certified Sales Professional (CSP) can be advantageous. Excellent communication, resilience, and relationship-building skills help you connect with healthcare professionals and navigate complex sales processes. These abilities ensure effective product promotion, customer trust, and success in a competitive, fast-paced market.

What are some common challenges faced by entry-level professionals in the medical device industry?

Entry-level professionals in the medical device industry often face challenges such as adapting to strict regulatory requirements, learning complex product details, and understanding clinical environments. They must quickly develop a strong grasp of medical terminology and device functions to effectively support sales teams or healthcare providers. Collaboration with cross-functional teams—such as engineering, quality assurance, and regulatory affairs—is essential, and strong communication skills help in navigating this dynamic environment. Overcoming these challenges can provide a solid foundation for career advancement within the industry.

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 Entry Level Medical Device jobs in Ohio?

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

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

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

What cities in Ohio are hiring for Entry Level Medical Device jobs?

Cities in Ohio with the most Entry Level Medical Device job openings:

Entry Level Medical Device jobs near you
Infographic showing various Entry Level Medical Device job openings in Ohio as of August 2026, with employment types broken down into 79% Full Time, 6% Part Time, and 15% Contract. Highlights an 100% In-person job distribution, with an average salary of $41,375 per year, or $19.9 per hour.

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

3 Key Consulting

New Albany, OH

$31 - $35/hr

Full-time

Posted 17 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.