Medical Devices OPT Jobs in Ohio
Ohio is a growing hub for medical devices F-1 OPT sponsorship jobs, with employers like Steris, Cardinal Health, and Philips Healthcare operating across Columbus, Cleveland, and Dayton. International students with OPT authorization in biomedical engineering, quality assurance, or regulatory affairs will find active hiring across both large manufacturers and specialized device companies throughout the state.
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Get Access To All JobsJOB 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.
EO/AA Employer Minorities/Females/Protected Veterans/Disabled
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.
EO/AA Employer Minorities/Females/Protected Veterans/Disabled
OPT Medical Devices Job Roles in Ohio
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Search Medical Devices Jobs in OhioMedical Devices OPT Sponsorship Jobs in Ohio: Frequently Asked Questions
Which medical devices companies sponsor F-1 OPT visas in Ohio?
Several established medical devices companies in Ohio have a track record of hiring F-1 OPT workers, including Steris in Mentor, Cardinal Health in Dublin, and Philips Healthcare in Highland Heights. Smaller contract manufacturers and device startups in the Columbus and Cleveland metro areas also hire OPT candidates, particularly for engineering, quality, and regulatory roles where specialized technical degrees are directly applicable.
Which cities in Ohio have the most medical devices F-1 OPT sponsorship jobs?
Columbus and Cleveland account for the largest share of medical devices OPT sponsorship jobs in Ohio. Columbus benefits from Cardinal Health's headquarters and a growing life sciences corridor, while Cleveland's proximity to the Cleveland Clinic has attracted numerous device and diagnostics companies. Dayton and Cincinnati also have active medical devices hiring, particularly in manufacturing and process engineering roles.
What types of medical devices roles typically qualify for F-1 OPT sponsorship?
Roles that align directly with a STEM degree field are the strongest fit for F-1 OPT authorization in medical devices. These include biomedical engineer, quality assurance engineer, regulatory affairs specialist, manufacturing engineer, and R&D scientist positions. Ohio employers filing under STEM OPT extension typically require candidates to hold degrees in biomedical engineering, mechanical engineering, electrical engineering, or life sciences from a STEM-designated program.
How do I find medical devices F-1 OPT sponsorship jobs in Ohio?
Migrate Mate is a job board built specifically for international students and visa holders, filtering listings by visa type and industry so you can search medical devices F-1 OPT sponsorship jobs in Ohio without sorting through roles that won't consider your status. Searching by the Medical Devices category and filtering to Ohio surfaces employers actively open to OPT candidates, saving significant time compared to general job searches.
Are there any Ohio-specific or industry-specific considerations for F-1 OPT sponsorship in medical devices?
Ohio's medical devices sector is heavily regulated, meaning many roles touch FDA-regulated products and require familiarity with quality management systems like ISO 13485 or 21 CFR Part 820. For STEM OPT extensions, students must confirm their degree program appears on the DHS STEM Designated Degree Program List and that their employer meets the formal training plan requirements under the I-983 form. Engaging your university's Designated School Official early is important for staying on track with filing deadlines.