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Biomedical R&D Engineer Jobs in Ohio (NOW HIRING)

Midmark

Senior Quality Engineer

Versailles, OH

$82K - $111K/yr

Leads cross-functionally with R+D engineering, manufacturing, technical service, and supply chain to manage quality, compliance and cost of medical devices and components. Will act as the subject ...

Midmark Corporation

Senior Quality Engineer

Versailles, OH · On-site

$82K - $111K/yr

Leads cross-functionally with R+D engineering, manufacturing, technical service, and supply chain to manage quality, compliance and cost of medical devices and components. Will act as the subject ...

Ranpak

Paper Engineer

Concord Township, OH

Research sustainability trends and regulatory requirements and provide technical advice to R amp;D/Engineering, sales/marketing and manufacturing teams. * Support the Automation business with ...

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All JobsBiomedical R&D Engineer JobsBiomedical R&D Engineer Jobs in Ohio

Biomedical R D Engineer information

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$39K

$90.1K

$133.1K

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

As of Jun 9, 2026, the average yearly pay for biomedical r&d engineer in Ohio is $90,133.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,800.00 and $110,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Biomedical R&D Engineer position, and why are they important?

Biomedical R&D Engineers require a solid background in biomedical engineering or a related field, with expertise in designing and testing medical devices or technologies. Familiarity with CAD software, laboratory instrumentation, statistical analysis tools, and relevant regulatory standards such as ISO 13485 or FDA guidelines is essential. Exceptional problem-solving abilities, teamwork, and strong communication skills are highly valued in this multidisciplinary environment. These competencies are critical for innovating safe and effective healthcare solutions and ensuring regulatory compliance in a complex, collaborative setting.

What is a Biomedical R&D Engineer job?

A Biomedical R&D Engineer is responsible for researching, designing, and developing medical devices, equipment, and technologies to improve healthcare. They apply engineering principles to solve biological and medical problems, often working with clinicians and scientists to create innovative solutions. Their tasks may include prototyping, testing, regulatory compliance, and improving existing medical technologies. This role requires strong knowledge of biomedical engineering, materials science, and physiology to ensure that solutions are safe, effective, and practical.

What are some typical challenges a Biomedical R&D Engineer may face in this role?

Biomedical R&D Engineers often encounter challenges such as meeting strict regulatory requirements, balancing innovation with safety, and ensuring designs are both functional and manufacturable. They may need to troubleshoot unexpected results during prototyping or testing, requiring creative thinking and technical flexibility. Close collaboration with clinical partners, regulatory specialists, and manufacturing teams is common, and effectively communicating across disciplines is key to overcoming hurdles. These challenges provide valuable learning opportunities and contribute to professional growth within the dynamic medical technology industry.

What are popular job titles related to Biomedical R&D Engineer jobs in Ohio? For Biomedical R&D Engineer jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Biomedical R&D Engineer jobs in Ohio look for? The top searched job categories for Biomedical R&D Engineer jobs in Ohio are:
Biomedical R D Engineer jobs near you
Infographic showing various Biomedical R&D Engineer job openings in Ohio as of May 2026, with employment types broken down into 74% Full Time, 13% Part Time, and 13% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $90,133 per year, or $43.3 per hour.
Senior Quality Engineer

Senior Quality Engineer

Midmark

Versailles, OH

$82K - $111K/yr

Full-time

Posted 25 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:

Leads the efforts to identify, investigate, plan, and conduct activities to improve or ensure quality through design and manufacturing of medical devices and components. Leads cross-functionally with R+D engineering, manufacturing, technical service, and supply chain to manage quality, compliance and cost of medical devices and components. Will act as the subject matter expert (SME) on elements within the quality department.

ESSENTIAL/PRIMARY DUTIES:

  • Ensures that products and product changes comply with all specified regulatory agencies (FDA, ISO, UL, CSA, etc.).
  • Creates and assists in developing, maintaining, and improving the Quality Management System (QMS) to ensure compliance to all specified regulatory agencies.
  • Drives product quality improvements internally and externally by working with design, manufacturing, and supply chain.
  • Acts as a technical lead, manages significant systems, uses strategic planning, and mitigates risk.
  • Formulates solutions to complex and ambiguous problems that are not well defined. Incorporates feedback and solutions from others.
  • Communicates complex technical ideas through daily work, presentations, and workshops.
  • Fosters cross team communication and knowledge sharing. Collaborates with teams and management to make critical technical decisions that align with organizational goals.
  • Collaborates with leadership and other cross functional departments to align decisions with organizational goals.
  • Champions six sigma techniques and drives standardization through continuous process improvement.

SECONDARY DUTIES:

  • Identifies and manages Six Sigma projects internal and external to the quality department as well as suppliers.
  • Provides leadership, coaching, and/or mentoring to the co-op group and level I, II & III engineers.
  • Supports, leads, or manages front room and/or back room for internal and external QMS audits and/or investigations.
  • Teaches and provides guidance on engineering documentation such as engineering drawings, bill of materials, change orders, testing documents and DHF/DMR records.

EDUCATION and/or EXPERIENCE:

Bachelor's degree in engineering or related field and 6+ years of relevant experience, or equivalent combination of both. Certified Quality Engineer (CQE), Six Sigma Blackbelt and Certified Reliability Engineer (CRE) certifications are preferred.

COMPETENCY and/or SKILL: 

  • Experience in the medical device industry and understanding of medical device quality systems and applications is desired
  • Ability to effectively influence and negotiate with all levels of an organization and lead effective/successful change initiatives
  • Ability to establish and enforce quality standards that align with industry best practices and regulatory requirements
  • Expert problem solver in areas of expertise
  • Ability to lead the design of complex, interconnected systems or processes and shape the organization's technical direction

SUPERVISORY RESPONSIBILITIES:

  • Provides leadership, coaching, and/or mentoring to level I, II and level III engineers.
  • May have direct reports of technicians or level I & 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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