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Medical Device Embedded System Engineer Jobs in Cincinnati, OH

iTech US, Inc.

Senior Medical Device Engineer

Blue Ash, OH · On-site

$96K - $131K/yr

Senior Medical Device Engineer PLM / Lifecycle Management Location: Blue Ash, OH Duration: 6+ ... Knowledge of Quality Management Systems (QMS), ISO 13485, FDA 21 CFR Part 820/QMSR, and regulatory ...

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Medical Device Embedded System Engineer information

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$60K

$131.7K

$184.2K

How much do medical device embedded system engineer jobs pay per year?

As of Sep 3, 2026, the average yearly pay for medical device embedded system engineer in Cincinnati, OH is $131,711.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,000.00 and $156,900.00 per year, depending on experience, location, and employer.

What does a medical device embedded system engineer do?

A Medical Device Embedded System Engineer designs, develops, and maintains the embedded software and hardware used in medical devices such as pacemakers, infusion pumps, and diagnostic equipment. They ensure that the systems meet strict safety, reliability, and regulatory standards required in the healthcare industry. Their work involves programming microcontrollers, integrating sensors and communication modules, and collaborating with cross-functional teams to ensure the final product is safe, effective, and compliant with medical regulations.

How does a medical device embedded system engineer typically collaborate with cross-functional teams during product development?

As a Medical Device Embedded System Engineer, you’ll work closely with teams such as hardware engineers, software developers, quality assurance, regulatory affairs, and clinical experts. Collaboration is essential to ensure the embedded system meets safety, performance, and regulatory requirements. This often involves participating in design reviews, troubleshooting integration issues, and providing technical documentation. Effective communication and teamwork are key, as you’ll be translating clinical needs into technical solutions and ensuring compliance with medical standards.

What are the key skills and qualifications needed to thrive as a medical device embedded system engineer, and why are they important?

A Medical Device Embedded System Engineer typically needs a strong background in electrical or computer engineering, experience with embedded C/C++ programming, and a solid understanding of medical device regulations. Familiarity with microcontrollers, real-time operating systems (RTOS), and compliance standards like IEC 62304 is highly valuable, and certifications in embedded systems or medical device software can be advantageous. Strong problem-solving skills, attention to detail, and effective teamwork are essential soft skills for excelling in this position. These competencies ensure the development of safe, reliable, and regulatory-compliant medical devices that improve patient outcomes.

What is the difference between Medical Device Embedded System Engineer vs Medical Software Engineer?

AspectMedical Device Embedded System EngineerMedical Software Engineer
CredentialsBachelor's or higher in Electrical, Computer Engineering, or related; knowledge of embedded systemsBachelor's or higher in Computer Science, Software Engineering, or related; programming skills
Work EnvironmentDesigning and testing embedded hardware/software for medical devicesDeveloping medical software applications, often on PCs or servers
Industry UsageUsed in medical devices like pacemakers, imaging equipment, and monitorsUsed in healthcare software, EHR systems, and medical data analysis

The Medical Device Embedded System Engineer focuses on developing embedded hardware and firmware for medical devices, ensuring safety and compliance. In contrast, the Medical Software Engineer primarily develops software applications used in healthcare settings. Both roles require technical expertise but differ in their focus on hardware versus software development within the medical industry.

What are popular job titles related to Medical Device Embedded System Engineer jobs in Cincinnati, OH?

For Medical Device Embedded System Engineer jobs in Cincinnati, OH, the most frequently searched job titles are:

What job categories do people searching Medical Device Embedded System Engineer jobs in Cincinnati, OH look for?

The top searched job categories for Medical Device Embedded System Engineer jobs in Cincinnati, OH are:

What cities near Cincinnati, OH are hiring for Medical Device Embedded System Engineer jobs?

Cities near Cincinnati, OH with the most Medical Device Embedded System Engineer job openings:

Medical Device Embedded System Engineer jobs near you
Infographic showing various Medical Device Embedded System Engineer job openings in Cincinnati, OH as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $131,711 per year, or $63.3 per hour.

Medical Device Electrical Hardware Engineer (Sustaining Engineering)- Blue Ash, OH Onsite

Siri InfoSolutions Inc

Blue Ash, OH • On-site

Contractor

Re-posted 29 days ago

Key responsibilities

  • Lead electrical engineering activities for sustaining and legacy medical device products.

  • Investigate and resolve electrical component obsolescence, supplier changes, and field issues.

  • Support design changes, verification/validation, and documentation updates in compliance with standards.

Job description

Greetings,
 
I hope this email finds you well. My name is Vinod. I came across your profile in our internal database/job boards, and based on your experience, I believe you could be an excellent fit for the following position with one of our clients, through an implementation partner.
 
Position: Medical Device Electrical Hardware Engineer (Sustaining Engineering)
Locations: Blue Ash, OH (Onsite from Day 1)
Duration: Long Term Contract
 
Role Descriptions: · Bachelor’s or master’s degree in electrical engineering or related field. · Minimum 6–8 years of experience in electrical engineering, with at least 3 years in a medical device or regulated industry. · Strong knowledge of analog/digital circuit design, Schematics, PCB layout, and troubleshooting. · Hands on experience on working with Sensors, Drivers, Microcontroller and different communication methodologies (On Board, Wired, Wireless etc.) · Experience with medical device standards (IEC 60601, ISO 13485, FDA QSR).
 
Must Have Technical/Functional Skills
 
Technical Skills
· Analog & Digital Circuit Design – Strong design and troubleshooting skills.
· Schematics and PCB Design Layout – Proficient in tools like Altium, OrCAD; knowledge of DFM/DFT.
· Component Engineering – Obsolescence management, alternate sourcing.
· Medical Standards Compliance – IEC 60601, ISO 13485, FDA 21 CFR Part 820.
· Failure Analysis – Root cause analysis (FMEA, 5 Whys, Fishbone). · Verification & Validation – Test planning, execution, and documentation. · Embedded Systems (Preferred) – Basic understanding of firmware/hardware integration. · Documentation & PLM Tools – BOMs, ECOs, DHF; tools like Agile, Windchill. Functional Skills · Sustaining Engineering – Support for legacy products and design updates. · Cross-Functional Collaboration – Work with QA, RA, Manufacturing, and Supply Chain. · Regulatory Knowledge – Understanding of global compliance requirements. · Project Management – Multitasking, prioritization, and milestone tracking. · Continuous Improvement – Lean/Six Sigma knowledge preferred.
 
Roles & Responsibilities
· Lead electrical engineering activities for sustaining and legacy medical device products.
· Investigate and resolve electrical component obsolescence, supplier changes, and field issues.
· Perform root cause analysis and implement corrective and preventive actions (CAPA).
· Support design changes, verification/validation, and documentation updates in compliance with FDA, ISO 13485, and IEC
60601 standards.
· Collaborate with cross-functional teams to ensure timely resolution of product issues and implementation of design
improvements.
· Participate in risk assessments (FMEA), design reviews, and change control processes.
· Provide technical support for manufacturing, test engineering, and quality assurance teams.
· Maintain and update technical documentation including schematics, BOMs, test protocols, and reports.
· Ensure compliance with regulatory requirements and internal quality systems.
Generic Managerial Skills, If any
· Strong communication skills. Candidates must be highly proficient in reading, writing, and speaking English language.
· Ability to multitask, including ability to understand customer requirements, retrieve relevant information, and provide
responses satisfactorily and with immediacy is required.
· Candidate must be able to effectively prioritize and manage multiple activities and responsibilities.
· Ability to understand and follow complex written procedures is required.
· Ability to function in a team environment and deliver on team objectives is required.
· Ability to make decisions and solve problems while exhibiting situational judgement.
Desirable Skills:
Keyword:
Skills: ISO 13485~EIS : Medical Device & Regulations~EIS : Embedded Digital Hardware Design and Development
Experience Required: 6-8
 
Please submit your resume with these details.
 
Candidate Full Name
 
Contact#:
 
Current Location:
 
Email id:
 
Work authorization:
 
Rate:
 
Timeslots for interview:
 
Availability to join:
 
 

Regards,

Thanks & Have a Blessed Day.

Vinod| Sr. IT Recruiter| Phone : 848-900-5968
Siri Infosolutions logo

About Siri Infosolutions

Sourced by ZipRecruiter

Our team of experts first gather each and every requirement of yours. Our research and development team then sit around those requirements and come up with a plan. Our implementation team then executes that plan for optimal results. After that our support team remains in constant touch with you during and after the entire process.

Industry

It services

Company size

201 - 500 Employees

Headquarters location

Edison, NJ, US

Year founded

2005

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