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Electrical Engineer Medical Device Jobs in Indiana

Flotec

Quality Engineer

Avon, IN · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Manufacturing Company Overview Flotec is an Indianapolis-based medical device manufacturer specializing in respiratory and oxygen delivery equipment. We manufacture ...

Hearst Health

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst Communications, Inc.

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

First Databank

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst Newspapers

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

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All JobsElectrical Engineer Medical Device JobsElectrical Engineer Medical Device Jobs in Indiana

Electrical Engineer Medical Device information

See Indiana salary details

$48.1K

$105.7K

$159.9K

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

As of Aug 6, 2026, the average yearly pay for electrical engineer medical device in Indiana is $105,710.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,000.00 and $125,600.00 per year, depending on experience, location, and employer.

Do electrical engineers work on medical devices?

Electrical engineers working in the medical device industry design and develop electronic components and systems used in medical equipment such as imaging devices, monitoring systems, and diagnostic tools. They often work with regulations, safety standards, and specialized tools like circuit simulation software to ensure device functionality and compliance.

What does an electrical engineer medical device do?

An Electrical Engineer in the medical device industry designs, develops, tests, and maintains electrical systems for medical equipment. They ensure compliance with regulatory standards, improve device performance, and collaborate with cross-functional teams to bring safe and effective products to market. Their work may involve circuit design, PCB layout, firmware development, and troubleshooting electrical components.

What are some typical challenges faced by electrical engineer medical device?

Electrical Engineers in the medical device field often encounter challenges such as ensuring regulatory compliance, managing strict quality standards, and designing for patient safety and reliability. Projects frequently involve interdisciplinary collaboration, requiring effective communication with mechanical engineers, software developers, and clinical experts to integrate complex systems. Additionally, engineers must stay up-to-date with evolving healthcare regulations and rapidly advancing medical technologies. Overcoming these challenges leads to rewarding work that directly impacts patient care and medical innovation.

What are the key skills and qualifications needed to thrive as an electrical engineer medical device?

To excel as an Electrical Engineer in the medical device industry, you typically need a degree in electrical engineering, solid experience in circuit design, and a working knowledge of medical device regulations. Familiarity with CAD tools, embedded systems, PCB design software, and certifications like ISO 13485 or experience with FDA compliance are often required. Strong problem-solving skills, collaborative teamwork, and effective communication make candidates stand out in this role. Mastering these areas is crucial for developing safe, innovative medical devices that comply with regulatory standards and improve patient outcomes.

What are the most commonly searched types of Electrical Engineer Medical Device jobs in Indiana? The most popular types of Electrical Engineer Medical Device jobs in Indiana are:
What are popular job titles related to Electrical Engineer Medical Device jobs in Indiana? For Electrical Engineer Medical Device jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Electrical Engineer Medical Device jobs in Indiana look for? The top searched job categories for Electrical Engineer Medical Device jobs in Indiana are:
Electrical Engineer Medical Device jobs near you
Infographic showing various Electrical Engineer Medical Device job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $105,710 per year, or $50.8 per hour.

Quality Engineer with Medical device

Kappium LLC

Warsaw, IN • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

 Start date: 24-Aug-2026  

Location: Warsaw, Indiana (hybrid role – 3 days onsite)

Duration: 9-12 months, extensions highly likely

Job:   Quality (software)  for Medical Device software 

Software Quality Engineer – Medical Device Software Development

Job Summary

The Software Quality Engineer will provide quality leadership on cross-functional product development teams responsible for developing regulated medical device software systems. This individual will serve as a subject matter expert in software quality, requirements management, software risk management, verification and validation strategy, design controls, and defect management throughout the software development lifecycle.

Key Responsibilities

  • Support the design, development, verification, and validation of regulated medical device software, including Software as a Medical Device (SaMD).
  • Provide technical leadership and guidance on software development processes, quality systems, and best practices.
  • Partner with engineering teams to refine software requirements and ensure architecture and design documentation is complete and compliant.
  • Facilitate documentation and tracking of software verification activities, including code review findings and testing results.
  • Review software test execution results, manage software defects, and support root cause investigations.
  • Lead software risk assessment activities and develop software risk management documentation.
  • Support regulatory submissions, product registrations, and compliance documentation.
  • Support internal and external quality audits and regulatory inspections related to software products and quality systems.
  • Manage nonconformances, CAPAs, and corrective actions associated with software development activities.
  • Provide technical support for software supplier and third-party software development audits.
  • Deliver training on software development processes, quality systems, and applicable regulatory requirements.
  • Mentor junior engineers and provide guidance on software quality engineering best practices.
  • Ensure compliance with applicable software and medical device standards, including:
    • IEC 62304
    • ISO 13485
    • ISO 14971
    • IEC 62366
    • FDA Software Guidance
    • FDA 21 CFR Part 11
    • EU MDR
    • ISO 27001
    • HIPAA
  • Ensure software products meet cybersecurity, privacy, electronic protected health information (ePHI), and personally identifiable information (PII) protection requirements.
  • Collaborate with cross-functional teams to ensure compliance with company quality systems, policies, and applicable regulatory requirements.
  • Communicate project risks, quality issues, and opportunities to leadership as appropriate.
  • Follow all health, safety, environmental, and quality procedures.
  • Perform additional responsibilities as assigned.

Education & Experience

  • Bachelor’s degree in Engineering, Computer Science, Information Systems, Biomedical Engineering, or a related technical discipline required.
  • Minimum of four years of experience in a regulated industry within software quality, quality engineering, new product development, or manufacturing engineering.
  • Experience supporting software development within a regulated medical device environment.
  • Demonstrated understanding of software quality systems, design controls, software verification and validation, and risk management.
  • Experience applying quality tools, processes, and methodologies to support product development.

Required Skills & Qualifications

  • Strong understanding of the medical device software development lifecycle.
  • Experience with Software as a Medical Device (SaMD) development preferred.
  • Knowledge of software risk management, design controls, software verification and validation, defect management, and CAPA processes.
  • Familiarity with FDA and international medical device regulations and standards.
  • Strong analytical, organizational, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work effectively on cross-functional engineering teams.
  • Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint.
  • ASQ Certified Software Quality Engineer (CSQE) or equivalent certification is preferred.

Apply