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R&D Engineer Medical Device Jobs in Ohio (NOW HIRING)

R+D Quality Engineer III

Versailles, OH

$66K - $86K/yr

JOB SUMMARY: The R + D Quality Engineer III leads and enforces product development quality ... Experience in the medical device industry and understanding of medical device quality systems and ...

R+D Quality Engineer III

Versailles, OH · On-site

$66K - $86K/yr

JOB SUMMARY: The R + D Quality Engineer III leads and enforces product development quality ... Experience in the medical device industry and understanding of medical device quality systems and ...

JOB RESPONSIBILITIES Living Safely • Actively participates in R&A monthly safety meetings ... JOB REQUIREMENTS MINIMUM QUALIFICATIONS: • Bachelor's degree in engineering or science field OR 3 ...

JOB RESPONSIBILITIES Living Safely Actively participates in R&A monthly safety meetings, quarterly ... Bachelor's degree in engineering or science field OR 3-5 years equivalent technical experience.

Senior Medical Device Engineer

Blue Ash, OH · On-site

$96K - $131K/yr

Senior Medical Device Lifecycle Engineer Location: Blue Ash, OH Duration: 6 Months Contract We are seeking an experienced Senior Medical Device Lifecycle Engineer to lead product lifecycle and ...

JOB SUMMARY: The R+D Verification Engineer II is a part of a team developing new products for the medical, dental and animal health markets. They design, document, and execute verification ...

Electrical Engineer

Cincinnati, OH · On-site

$50 - $60/hr

We are seeking an experienced Electrical / Embedded Hardware Engineer with 5+ years of hands-on experience in medical device product development, embedded hardware engineering, electrical design ...

Senior Medical Device Engineer

Blue Ash, OH · On-site

$96K - $131K/yr

Senior Medical Device Engineer PLM / Lifecycle Management Location: Blue Ash, OH Duration: 6+ Months Contract 7+ years of engineering experience in medical device or other regulated industries.

This engineer position plays a key role in product and process development, customer technical ... Demonstrated commitment to Inclusion & Diversity: our I&D aspiration is that all employees are ...

The Product Research and Development Engineer drives advancements that will lead to the improvement of existing products as well as the development of the next generation of products. This position ...

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R D Engineer Medical Device information

See Ohio salary details

$58K

$83.3K

$118.4K

How much do r&d engineer medical device jobs pay per year?

As of Sep 6, 2026, the average yearly pay for r&d engineer medical device in Ohio is $83,256.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,273.00 and $99,639.00 per year, depending on experience, location, and employer.

What is an R&D engineer medical device?

An R&D Engineer in the medical device industry is responsible for designing, developing, and testing new medical technologies to improve patient care. They work on product innovation, prototyping, and regulatory compliance to ensure medical devices meet industry standards. Their role involves collaboration with cross-functional teams, including healthcare professionals and manufacturing specialists, to bring safe and effective products to market. Additionally, they conduct research, analyze data, and troubleshoot issues to enhance device performance and reliability.

What are the key skills and qualifications needed to thrive as an R&D engineer medical device?

To thrive as an R&D Engineer Medical Device, you should have a strong background in engineering disciplines such as biomedical, mechanical, or electrical engineering, typically with a relevant bachelor's or master's degree. Familiarity with CAD software, prototyping tools, regulatory standards (such as ISO 13485 or FDA requirements), and design verification/validation processes is essential. Key soft skills include problem-solving, creativity, teamwork, and effective communication to collaborate with multidisciplinary teams and stakeholders. These skills and qualities ensure innovative, safe, and compliant products are developed efficiently and brought successfully to market.

What are some common challenges faced by R&D engineers in the medical device industry?

R&D Engineers in the medical device field often navigate challenges such as meeting stringent regulatory requirements, balancing innovation with safety, and working under tight development timelines. They regularly collaborate with cross-functional teams including clinicians, regulatory specialists, and manufacturing engineers to ensure product feasibility and compliance throughout the design process. Adapting quickly to evolving regulations and new technological advancements is also part of the role. These challenges make the job dynamic and require continuous learning and strong teamwork, but they also contribute to making meaningful and impactful products in healthcare.

What cities in Ohio are hiring for R&D Engineer Medical Device jobs?

Cities in Ohio with the most R&D Engineer Medical Device job openings:

Infographic showing various R&D Engineer Medical Device job openings in Ohio as of August 2026, with employment types broken down into 57% Full Time, and 43% Contract. Highlights an 100% In-person job distribution, with an average salary of $83,256 per year, or $40 per hour.

R+D Quality Engineer III

Midmark

Versailles, OH

$66K - $86K/yr

Full-time

Re-posted 19 days ago


Midmark rating

9.1

Company rating: 9.1 out of 10

Based on 13 frontline employees who took The Breakroom Quiz


Job description

JOB SUMMARY:

The R + D Quality Engineer III leads and enforces product development quality initiatives through identifying, investigating, planning, and conducting activities aimed at insuring robust and quality design and manufacturability of medical devices.

ESSENTIAL/PRIMARY DUTIES:

  • Plans, leads, and manages quality deliverables on new product development (NPD) projects in accordance with regulatory standards ISO9001:2015, ISO13485:2016, ISO14971, FDA, CSA, and EU MDR regulations.
  • Leads all risk management processes and creates risk management documentation for (NPD) projects.
  • Creates, reviews, and approves documentation related to the engineering Product Realization Process (PRP). Documentation includes, but is not limited to, change requests, engineering orders, product and component test specifications and design records.
  • Facilitates the design and process failure mode and effects analysis (FMEA) process.
  • Leads site-based quality department initiatives as a subject matter expert (SME).
  • Applies domain expertise to the application and advancement of engineering methods and tools. Leads the application of six sigma techniques and drives continuous process improvement.
  • Collaborates with cross-functional teams to align decisions with business goals.
  • Mentors engineer I & II teammates, focusing on technical skills, collaboration skills, and cultural competencies.
  • Applies advanced tools and methods to solve complex problems. Tackles technical challenges and contributes to troubleshooting effort.

SECONDARY DUTIES:

  • Supports internal and external quality system audits.
  • Leads the creation of threat models and cybersecurity risk assessments.
  • Leads the creation and maintenance of the products Usability Engineering Files, provides misuse cases involving use error and assesses the impact.
  • Assists with the creation of the reliability predictions for projects with recommended testing profiles and analyzes test results.

EDUCATION and/or EXPERIENCE:

Bachelor's degree in engineering or related field and 4+ years of relevant experience, or equivalent combination of both. Certified Quality Engineer (CQE), Six Sigma Blackbelt (DMAIC, DMADV), and Certified Reliability Engineer (CRE) certifications preferred.

COMPETENCY and/or SKILL:

  • Experience in the medical device industry and understanding of medical device quality systems and applications is desired.
  • Mastery of software programs - Microsoft Word, PowerPoint, Excel, Project, Minitab
  • Strong written and verbal communication skills
  • Ability to apply advanced analytical tools and methods to solve complex problems
  • Ability to lead the design of complex systems and identify new technological opportunities

SUPERVISORY RESPONSIBILITIES:

  • Provides leadership, coaching, and/or mentoring to level I and level II engineers.

Founded in 1915, Midmark Corporation is the only company transforming healthcare experiences through innovative design within the medical, dental and animal health environments. With more than 2,200 teammates worldwide, Midmark focuses on harmonizing space, technology and workflows, creating a better experience for caregivers and patients at the point of care. The Midmark headquarters and innovation hub are located in Versailles, Ohio, which is also home to the Midmark Experience Center, Design Center, Technology Center and our largest manufacturing facility. Midmark maintains eleven additional locations in the United States, including four innovation hubs, and has subsidiaries in India and Italy.

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