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Engineering Medical Device Jobs in Ohio (NOW HIRING)

PB consulting

OH · On-site

Lead component development and engineering change projects from concept to implementation. * Manage ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:

iTech US, Inc.

Senior Medical Device Engineer

Blue Ash, OH · On-site

$96K - $131K/yr

Blue Ash, OH Duration: 6+ Months Contract 7+ years of engineering experience in medical device or other regulated industries. Experience leading cross-functional technical projects. Experience with ...

PB consulting

Lead component development and engineering change projects from concept to implementation. * Manage ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:

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All JobsEngineering Medical Device JobsEngineering Medical Device Jobs in Ohio

Engineering Medical Device information

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$20

$47

$91

How much do engineering medical device jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for engineering medical device in Ohio is $47.38, according to ZipRecruiter salary data. Most workers in this role earn between $33.37 and $56.68 per hour, depending on experience, location, and employer.

What is an engineering medical device professional?

Engineering medical device professionals are specialists who design, develop, test, and improve medical devices used in healthcare. They combine principles of engineering, biology, and medicine to create equipment such as pacemakers, imaging machines, and prosthetics that help diagnose, treat, or manage medical conditions. Their work ensures devices are safe, effective, and comply with regulatory standards. These professionals often work closely with doctors, patients, and regulatory agencies throughout the product development process.

What are the key skills and qualifications needed to thrive as a medical device engineer?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant degree and knowledge of FDA regulations. Familiarity with CAD software, prototyping tools, and quality management systems is typically required, along with certifications like Six Sigma or ISO 13485. Strong problem-solving abilities, teamwork, and effective communication are standout soft skills in this role. These competencies are crucial for designing safe, innovative devices that meet regulatory standards and improve patient outcomes.

What are some typical challenges faced by engineers working in the medical device industry?

Engineers in the medical device industry often face challenges related to strict regulatory compliance, such as meeting FDA or ISO standards. Additionally, they must ensure that devices are safe, effective, and user-friendly, requiring frequent collaboration with cross-functional teams like clinical, quality assurance, and manufacturing. Balancing innovation with patient safety while managing tight project timelines is also a common aspect of the role. Overcoming these challenges can be rewarding, as it directly contributes to improving patient outcomes.

What is the difference between Engineering Medical Device vs Biomedical Engineer?

AspectEngineering Medical DeviceBiomedical Engineer
Required CredentialsEngineering degree, possibly certifications in medical device designEngineering or biomedical degree, certifications in healthcare technology
Work EnvironmentDesign labs, manufacturing facilities, regulatory agenciesHospitals, research labs, healthcare companies
Employer & Industry UsageMedical device companies, biotech firms, regulatory bodiesHospitals, medical research institutions, healthcare technology firms

Engineering Medical Device professionals focus on designing, developing, and testing medical devices, often working in manufacturing or regulatory settings. Biomedical Engineers have a broader scope, integrating engineering principles with biological sciences to improve healthcare solutions, including medical devices. While both roles require engineering backgrounds, Engineering Medical Device specialists typically concentrate on product development, whereas Biomedical Engineers may work on research, clinical applications, or device integration.

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

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

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

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

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

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

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

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

Engineering Medical Device jobs near you
Infographic showing various Engineering Medical Device 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 $98,551 per year, or $47.4 per hour.

Medical Device Component Development Engineer

PB consulting

Miamiville, OH • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

We are seeking a Medical Device Component Development Engineer to support component development, product lifecycle management, and engineering change activities for regulated medical devices. The ideal candidate will have expertise in design controls, verification & validation, supplier quality, process validation, and regulatory compliance.

Roles and Responsibilities
  • Lead component development and engineering change projects from concept to implementation.
  • Manage project timelines, risks, and cross-functional coordination.
  • Support Design Verification & Validation (V&V), test protocols, and technical documentation.
  • Partner with suppliers on component qualification, DFM reviews, tooling, and process capability.
  • Support manufacturing transfer, IQ/OQ/PQ, pilot builds, and production readiness.
  • Apply Design Controls, PLM, ECO/ECN/ECR, Risk Management, and Quality System requirements.
  • Review engineering drawings, GD&T, specifications, and acceptance criteria.
  • Drive root cause analysis using CAPA, 8D, 5 Whys, and Fishbone methodologies.
  • Communicate project status, risks, and technical recommendations to stakeholders.
Required Qualifications
  • Experience in Medical Device Component Development or Product Development.
  • Strong knowledge of:
    • Product Lifecycle Management (PLM)
    • Design Controls & Engineering Change Management (ECO/ECN/ECR)
    • Design Verification & Validation (V&V)
    • ISO 14971, DFMEA, PFMEA
    • ISO 13485 & FDA 21 CFR Part 820/QMSR
    • Supplier Quality Engineering & Design for Manufacturability (DFM)
    • Process Validation (IQ/OQ/PQ)
    • GD&T and engineering drawings
  • Strong project management, communication, and problem-solving skills.
  • Experience working with cross-functional teams in a regulated medical device environment.
Preferred Skills
  • Medical Device Product Development
  • Supplier Quality & Component Qualification
  • Risk Management & Regulatory Compliance
  • Manufacturing Transfer & Validation
  • Root Cause Analysis (CAPA, 8D)
  • Stakeholder & Project Management

Apply