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Process Engineer Medical Device Jobs in Ohio (NOW HIRING)

As the Process Engineer, you are a part of Best People. You will utilize our Best Systems to gather ... Medical, Dental, Vision, and Life Insurance Coverage begin on the first day of full-time employment

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 ...

... 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

Process Engineer

Columbus, OH · On-site

$85K - $130K/yr

... 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

The Process Engineer manages project and works closely with the department in the development and ... If, because of a medical condition or disability, you need a reasonable accommodation for any part ...

The Process Engineer manages project and works closely with the department in the development and ... If, because of a medical condition or disability, you need a reasonable accommodation for any part ...

Process Engineer - Forging Location: Canton, Ohio Company: Canton Drop Forge, Inc. Canton Drop ... Canton Drop Forge offers a comprehensive and competitive benefit package including medical, dental ...

Process Engineer - Forging Location: Canton, Ohio Company: Canton Drop Forge, Inc. Canton Drop ... Canton Drop Forge offers a comprehensive and competitive benefit package including medical, dental ...

The Process Engineer will develop and improve plating and chemical processes for the production of ... Benefit options include medical, dental, vision, 401K, Flexible Spending Account, Health Savings ...

The Process Engineer will develop and improve plating and chemical processes for the production of ... Benefit options include medical, dental, vision, 401K, Flexible Spending Account, Health Savings ...

The Process Engineer is an integral part of the autonomous work teams that make up the production ... If, because of a medical condition or disability, you need a reasonable accommodation for any part ...

Cenovus is seeking a Process Engineer to provide technical leadership for the South Complex Area ... Medical & dental coverage * Life insurance * Disability benefits * Employee assistance program

New

You are a Manufacturing Process Engineer that can lead the development, deployment, and continuous ... Health Insurance including Medical, Dental and Vision * 401k * Paid Time off * Parental and ...

Showing results 21-40

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 Aug 8, 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 skills and qualifications are needed to thrive as a process engineer medical device?

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 does a process engineer medical device do?

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?

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.

Infographic showing various Process Engineer Medical Device job openings in Ohio as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $87,481 per year, or $42.1 per hour.

Medical Device Quality Engineer at Blue Ash, OH

Volto USA

Blue Ash, OH • On-site

$66K - $85K/yr

Contractor

Posted 8 days ago


Job description

Role: Medical Device Quality Engineer 
Location: Blue Ash, OH
Duration: 6 months
Role Descriptions:
· 7+ years of engineering experience in medical device or other regulated industries. · Experience leading cross-functional technical projects. ·
Experience with component development, supplier qualification, design verification, and manufacturing validation. · Strong understanding of design controls, change management, risk management, process validation, and quality system compliance.
Must Have Technical/Functional Skills
· Strong expertise in Medical Device Product Lifecycle Management (PLM), Design Controls, and Engineering Change Management (ECO/ECN/ECR).
· Hands-on experience with Design Verification & Validation (V&V), test methods, protocol development, and technical documentation.
· Deep understanding of Risk Management methodologies, including ISO 14971, DFMEA, PFMEA, and hazard analysis.
· Knowledge of Quality Management Systems (QMS), ISO 13485, FDA 21 CFR Part 820/QMSR, and regulatory compliance requirements.
· Experience in Supplier Quality Engineering, component qualification, supplier development, and Design for Manufacturability (DFM). · Proficiency in Process Validation activities including IQ/OQ/PQ, pilot builds, validation builds, and manufacturing transfer. · Ability to interpret engineering drawings, GD&T, tolerance stack-ups, specifications, and acceptance criteria. · Strong root cause analysis and problem-solving skills utilizing 8D, CAPA, 5 Why, Fishbone, and corrective action processes. · Excellent project management skills, including planning, scheduling, risk management, stakeholder management, and cross-functional coordination. · Effective leadership, communication, and influencing skills, with the ability to drive decisions and deliver results without direct authority.
Roles & Responsibilities
· Lead multiple high-priority lifecycle change projects from concept through implementation.
· Drive project plans, timelines, risk mitigation strategies, and implementation readiness.
· Coordinate cross-functional teams across Engineering, Quality, Regulatory, Manufacturing, Supply Chain, Procurement, Operations, and external suppliers.
· Serve as the technical interface with suppliers for component development, DFM reviews, tooling readiness, process capability, and component qualification.
· Support design verification and validation activities, including test planning, execution, data review, and  technical documentation.
· Partner with manufacturing sites on process validation activities, including IQ/OQ/PQ, pilot builds, validation builds, and production launch readiness.
· Apply strong knowledge of design controls, engineering change management, risk management, quality system requirements, and regulatory expectations.
· Review engineering drawings, specifications, GD&T requirements, tolerance analyses, and component acceptance criteria.
· Drive root cause analysis, technical problem solving, and timely closure of project issues.
· Communicate project status, risks, decisions, and recommendations clearly to stakeholders and senior leadership.
· Demonstrate strong ownership, urgency, accountability, and ability to influence without direct authority.
Generic Managerial Skills, If any
· Strong communication skills, with proficiency in reading, writing, and speaking English.
· Ability to multitask, understand customer requirements, and respond promptly and accurately.
· Capability to prioritize and manage multiple tasks in a fast‑paced environment.
· Ability to understand and follow complex written procedures.
· Ability to work effectively in a team environment and contribute to team goals.
· Strong decision‑making and problem‑solving abilities with sound situational judgment.
Essential Skills: EIS : MDD Risk Management
Desirable Skills: