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Biomaterials Engineer Jobs in Ohio (NOW HIRING)

Deep knowledge of biomechanics, biomaterials, bioinstrumentation, medical imaging, tissue engineering, physiological systems modeling, biostatistics, and regulatory affairs. Ability to explain signal ...

Deep knowledge of biomechanics, biomaterials, bioinstrumentation, medical imaging, tissue engineering, physiological systems modeling, biostatistics, and regulatory affairs. Ability to explain signal ...

Deep knowledge of biomechanics, biomaterials, bioinstrumentation, medical imaging, tissue engineering, physiological systems modeling, biostatistics, and regulatory affairs. Ability to explain signal ...

Deep knowledge of biomechanics, biomaterials, bioinstrumentation, medical imaging, tissue engineering, physiological systems modeling, biostatistics, and regulatory affairs. Ability to explain signal ...

Research Senior Technician

Columbus, OH · On-site

$17.50 - $24/hr

Specific Research Areas that the Research Lead Technician will be involved in will include working with graduate student and research engineers to fabricate and characterize biomaterials. They will ...

... Engineering, or related field. * 0-2 years of relevant work experience * Experience with synthesis, purification, and characterization of polymeric materials, biomaterials, and/or nanoparticles.

... Engineering, or related field. * 0-2 years of relevant work experience * Experience with synthesis, purification, and characterization of polymeric materials, biomaterials, and/or nanoparticles.

Biomaterials Engineer information

See Ohio salary details

$41.8K

$101.1K

$164.9K

How much do biomaterials engineer jobs pay per year?

As of Aug 17, 2026, the average yearly pay for biomaterials engineer in Ohio is $101,141.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,300.00 and $126,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a biomaterials engineer, and why are they important?

A successful Biomaterials Engineer typically holds a degree in biomedical engineering, materials science, or a related field, with expertise in material properties, biological interactions, and design principles. Familiarity with tools such as CAD software, laboratory instrumentation, and regulatory standards (like ISO 10993 or FDA guidelines) is crucial. Strong problem-solving skills, teamwork, and effective communication abilities help Biomaterials Engineers excel in collaborative and multidisciplinary environments. These competencies are vital to ensure the safe, effective, and innovative development of materials for use in medical devices or biomedical applications.

What are some typical projects or responsibilities I would handle as a biomaterials engineer?

As a Biomaterials Engineer, you'll often work on developing, testing, and improving materials for use in medical implants, tissue engineering, drug delivery systems, or diagnostic devices. Your daily responsibilities may include conducting laboratory experiments, analyzing biological and chemical data, and collaborating with clinicians, biologists, and product designers to optimize material performance. You may also participate in regulatory documentation and help ensure products meet safety and compliance standards. Projects often require cross-functional teamwork, creativity, and staying updated with advances in biomaterials science.

What does a biomaterials engineer do?

A Biomaterials Engineer designs, develops, and tests materials used in medical devices, implants, and tissue engineering applications. They work with biocompatible substances such as polymers, ceramics, and metals to ensure they interact safely with the human body. Their role involves conducting research, improving existing biomaterials, and collaborating with medical professionals to create innovative healthcare solutions. Biomaterials Engineers often work in medical device companies, research institutions, or pharmaceutical firms.

How much does a biomaterials engineer make?

The average salary for a biomaterials engineer typically ranges from $70,000 to $110,000 annually, depending on experience, education, and location. Professionals in this field often work in research labs, medical device companies, or biotech firms, and advanced skills or certifications can lead to higher compensation.

What are popular job titles related to Biomaterials Engineer jobs in Ohio?

For Biomaterials Engineer jobs in Ohio, the most frequently searched job titles are:

What cities in Ohio are hiring for Biomaterials Engineer jobs?

Cities in Ohio with the most Biomaterials Engineer job openings:

Infographic showing various Biomaterials Engineer job openings in Ohio as of August 2026, with employment types broken down into 90% Full Time, 2% Part Time, and 8% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $101,141 per year, or $48.6 per hour.

Head of Biosensor Development

Kilele Health Inc.

Cincinnati, OH • On-site

$180 - $280/hr

Other

Posted 12 days ago


Job description

Head of Biosensor DevelopmentMust Haves for this Position
  • Formal education in Biomedical Engineering, Materials Science, Chemical Engineering, Electrical Engineering, Mechanical Engineering, or a related field with a substantial combination of degree level (BS/MS/PhD) and relevant work experience
  • Demonstrated leadership developing Class II or higher electrochemical sensors from concept through manufacturing transfer, including direct expertise in one or more elements of electrochemical sensing (e.g. electrochemistry, sensor manufacturing processes, biomaterials, dried reagent chemistries, voltammetry/amperometry).

While we always appreciate interest in our Company, if you do not meet the above criteria, we urge you to spend your efforts on a role with a higher probability of success for you, thanks!

The Position

The Head of Biosensor Development leads the development of Kilele Health's wearable biosensor sensing element – the electrochemical microstrip with active reagent chemistry present. This role will work closing with the Head of Hardware/Software to create fully developed wearable biosensors based on regenerative aptamer chemistries.

The Head of Biosensor Developmentis responsible for the design, development, verification, validation, and manufacturing readiness of the microstrip sensing element subsystem, ensuring it meets performance, quality, reliability, and scalability objectives. Working closely with aptamer development, electronics, manufacturing, quality, regulatory, and clinical, this role translates innovative sensor concepts into robust, manufacturable products.

Leadership & Strategy
  • Define and execute the technical strategy and development roadmap for the sensor subsystem from plated electrodes through transmitter integration.
  • Build, lead, mentor, and develop a multidisciplinary sensor development team while fostering a culture of innovation, collaboration, accountability, and technical excellence.
  • Establish development priorities, resource plans, and departmental budgets aligned with product development objectives.
  • Manage technical risks, development timelines, and project execution to achieve key milestones on time and in budget.
  • Evaluate emerging materials, manufacturing methods, and technologies to improve sensor performance, manufacturability, and reliability.
Sensor Development
  • Lead the development and optimization of sensor manufacturing methods, test procedures, and assembly processes.
  • Develop process controls and strategies that improve consistency, yield, quality, and scalability.
  • Support sensor prototype builds as needed.
  • Partner with Manufacturing to ensure successful technology transfer and continuous process improvement.
  • Lead investigations into sensor performance issues and implement corrective actions that improve product robustness and manufacturability.
Verification, Validation & Manufacturing Readiness
  • Define and oversee verification and validation strategies for the sensor subsystem.
  • Develop quality control methods, reliability testing protocols, and performance characterization strategies.
  • Ensure development activities support design controls, quality system requirements, and regulatory submissions.
Cross-Functional Development
  • Collaborate with aptamer development, electronics, manufacturing, quality, regulatory, and clinical teams to deliver integrated product solutions.
  • Partner with systems and electronics engineers to optimize sensor performance through transmitter integration.
  • Analyze experimental, manufacturing, and clinical data to guide design decisions, process improvements, and product performance.
  • Communicate technical strategy, project status, risks, and resource needs to executive leadership to support strategic planning and decision-making.
Technical QualificationsRequired
  • Ph.D. in Biomedical Engineering, Materials Science, Chemical Engineering, Electrical Engineering, Mechanical Engineering, or a related field with 5+ years of relevant industry experience; or M.S. with 10+ years of experience. B.S. with exceptionally relevant work experience will be considered.
  • Demonstrated leadership developing Class II or higher electrochemical sensors from concept through manufacturing transfer, including direct expertise in one or more elements of electrochemical sensing (e.g. electrochemistry, sensor manufacturing processes, biomaterials, dried reagent chemistries, voltammetry/amperometry).
  • Experience developing products within a regulated medical device quality system.
  • Experience leading cross-functional product development teams in a fast-paced R&D environment.
  • Strong understanding of design controls, verification, validation, risk management, and manufacturing readiness.
  • Experience with project management, budget management, and personnel management.
Preferred
  • Experience developing continuous monitoring sensors (CGM or analogous electrochemical wearable sensors, e.g. wearable or implantable).
  • Experience with statistical analysis and Design of Experiments (DOE).
  • Experience supporting clinical studies and regulatory submissions.
  • Experience scaling manufacturing processes from prototype through commercial production.
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