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Process Engineer Medical Device Jobs in Ohio (NOW HIRING)

ConfigUSA

Medical Device Support

Blue Ash, OH · On-site

... processes| and software-driven system Essential Skills: Ethicon Project Support Desirable Skills: Keyword: Skills: EIS : Medical Device & Regulations~EIS : Manufacturing Engineering Support

Axogen

Sr. Engineer, Manufacturing/Processing

Vandalia, OH

$97K - $126K/yr

Medical device, biologic or HCTP experience * A minimum of 5 years experience in Manufacturing Engineering, Process Design Engineering, Process Optimization, or Process Development preferably with a ...

Centor

Process Engineer

Millersburg, OH

$80K - $90K/yr

... and medical devices as well as solutions for the health industry. The product range includes ... Process Engineer Reports To: Operations Manager Location: Berlin, Ohio Industry: Packaging ...

Cleveland-Cliffs, Inc.

Process Engineer

Middletown, OH · On-site

The Process Engineer is responsible for providing daily processing information to the Department ... If, because of a medical condition or disability, you need a reasonable accommodation for any part ...

fi

Process Engineer

Columbus, OH · On-site

... Process Engineer. This position is responsible for the optimization of existing processes and the ... Medical/dental/vision insurance * Life insurance * On-site fitness center staffed by trainers

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All JobsProcess Engineer Medical Device JobsProcess Engineer Medical Device Jobs in Ohio

Process Engineer Medical Device information

See Ohio salary details

$47.1K

$87.5K

$135.5K

How much do process engineer medical device jobs pay per year?

As of Jun 14, 2026, the average yearly pay for process engineer medical device in Ohio is $87,481.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,800.00 and $97,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Process Engineer Medical Device position, and why are they important?

A Process Engineer in Medical Devices typically requires a degree in engineering (such as chemical, biomedical, or mechanical engineering) and experience with manufacturing processes, quality systems, and regulatory compliance. Familiarity with tools like CAD software, statistical analysis programs, lean manufacturing techniques, and knowledge of standards such as ISO 13485 are common requirements. Strong problem-solving abilities, project management skills, and excellent communication facilitate successful interactions with cross-functional teams. These skills ensure efficient, high-quality, and compliant manufacturing processes critical to patient safety and company success.

What are some common projects or responsibilities I might take on as a Process Engineer in the medical device industry?

As a Process Engineer in the medical device industry, you'll commonly work on projects such as optimizing manufacturing processes, implementing new technologies, and ensuring compliance with strict quality and regulatory standards. Your daily tasks may include designing and validating production methods, troubleshooting process issues, and collaborating closely with quality assurance, R&D, and production teams. You may also be involved in documentation, process scale-up for new products, and continuous improvement initiatives. The role is highly collaborative, requiring you to coordinate with both technical and non-technical staff to meet quality, efficiency, and regulatory goals.

What is a Process Engineer Medical Device job?

A Process Engineer in the medical device industry is responsible for designing, implementing, and optimizing manufacturing processes to ensure efficiency, quality, and compliance with regulatory standards. They work to improve production procedures, troubleshoot issues, and develop new process technologies. Their role involves collaborating with cross-functional teams, such as design, quality, and regulatory, to ensure medical devices meet industry requirements. Additionally, they analyze data, validate processes, and support continuous improvement initiatives to enhance product reliability and manufacturing scalability.

What are popular job titles related to Process Engineer Medical Device jobs in Ohio? For Process Engineer Medical Device jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Process Engineer Medical Device jobs in Ohio look for? The top searched job categories for Process Engineer Medical Device jobs in Ohio are:
Process Engineer Medical Device jobs near you

Process /Manufacturing Engineer - US Citizen / Green Card Holder

Techtrueup

Cincinnati, OH • On-site

Contractor

Posted 28 days ago

Job description

Company Description
Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE-certified Healthcare Staffing and Engineering Services provider supporting industries including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food & Beverage, and Automotive. We proudly partner with 120+ clients such as Johnson & Johnson, Haemonetics, Delta, Caterpillar, Artisan Chef, Baxter, and many more. Our wide network of consultants and contract-to-hire engineers brings deep expertise across Engineering, Technical, Administrative, Healthcare, Life Sciences, Blue Collar, Skilled Trades, IT, Software Development, Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software's enabling us to source and screen top talent within hours. This ensures rapid response times, high-quality matches, and virtually zero attrition.
Job Description
Job Title : Process Engineer - Medical Device Industry
Location : Cincinnati, OH (Onsite)
Duration : 12 Months
Need US Citizens for this opportunity
Travel to Mexico / Ireland / Singapore
Overview
Seeking a Contract Process Engineer to support the design, development, optimization, and scale-up of
manufacturing processes for medical device and drug-delivery components. The contractor will work
with cross-functional teams and suppliers to deliver robust, manufacturable solutions.
Key Responsibilities
  • Develop, optimize, and validate component and assembly manufacturing processes.
  • Support DFM/A activities and translate product requirements into process outputs.
  • Conduct process characterization, capability studies, and statistical analyses.
  • Partner with R&D, Quality, Regulatory, Supplier Engineering, and Operations throughout development.
  • Support equipment debug, characterization, FAT, and qualification activities.
  • Troubleshoot manufacturing and compliance issues and support process transfer to production sites.

Preferred Background
  • 6+ years in process development within a regulated industry.
  • Strong understanding of component fabrication and assembly processes.
  • Experience with DFMA, FMEA, and applied statistics (MSA, process capability).
  • Experience with equipment commissioning (debug, characterization, FAT, validation).
  • Familiarity with Lean, Six Sigma, or similar methodologies.
  • Experience supporting commercialization or working with global teams/suppliers.
  • Prior J&J or MedTech experience is strongly preferred.

Qualifications
Additional Information
All your information will be kept confidential according to EEO guidelines.

Apply