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Medical Device Software Jobs (NOW HIRING)

Cesna Recruitment

Senior Software Engineer

San Diego, CA

$130K - $171K/yr

[Position] Senior Software Engineer [About Our Client] Research & Development hub for artificial ... As medical device development is iterative and subject to regulatory, technical, and business ...

Intuvie

Senior SQA Engineer

Natick, MA · On-site

$120K - $130K/yr

Participate in verification, testing, and documentation of medical device software per governing SOPs * Document verification procedures, verification results and traceability matrices. * Develop ...

US Tech Solutions

Software Engineer III

Monroeville, PA

$57 - $76.50/hr

Analyzing and verifying medical device designs. * *Writing detailed automated and manual test procedures that evaluate medical device software and systems against documented requirements. * *Writing ...

Intuvie

Senior SQA Engineer

Natick, MA · On-site

$120K - $130K/yr

Participate in verification, testing, and documentation of medical device software per governing SOPs * Document verification procedures, verification results and traceability matrices. * Develop ...

AbbVie

Device Software Engineer

North Chicago, IL

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... software development background in a structured/regulated environment such as medical device ...

AbbVie

Device Software Engineer

Irvine, CA

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... software development background in a structured/regulated environment such as medical device ...

AbbVie

Device Software Engineer

North Chicago, IL · On-site

$109K/yr

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... software development background in a structured/regulated environment such as medical device ...

AbbVie

Device Software Engineer

Irvine, CA

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... software development background in a structured/regulated environment such as medical device ...

AbbVie

Device Software Engineer

Irvine, CA · On-site

$109K/yr

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... software development background in a structured/regulated environment such as medical device ...

US Tech Solutions

C#/Java Developer

Monroeville, PA

Conduct Manual and Automated Design V&V activities as an active member of scrum project teams designing and developing medical device software, intended for use by patients with sleep and respiratory ...

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Medical Device Software information

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How much do medical device software jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for medical device software in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Device Software Engineer, and why are they important?

To thrive as a Medical Device Software Engineer, you need strong programming abilities (often in C/C++ or Python), a solid understanding of software development life cycles, and familiarity with medical device regulations, typically backed by a degree in computer science, engineering, or a related field. Experience with development tools, embedded systems, and compliance standards like IEC 62304 or FDA requirements is highly valued. Attention to detail, problem-solving, and effective teamwork are essential soft skills in this role. These competencies ensure the creation of reliable, safe, and regulatory-compliant software critical for patient health and device performance.

What is the highest paying medical tech job?

In the field of medical device software, senior roles such as Medical Software Engineering Managers or Director of Medical Software typically have the highest salaries, often exceeding six figures. These positions require advanced technical skills, experience in regulatory compliance, and leadership abilities, reflecting their seniority and responsibility within medical technology companies.

What is the difference between Medical Device Software vs Medical Device Quality Assurance Specialist?

AspectMedical Device SoftwareMedical Device Quality Assurance Specialist
Required CredentialsSoftware development certifications, engineering degrees, FDA regulations knowledgeQuality assurance certifications (e.g., CQE), regulatory compliance training
Work EnvironmentSoftware development teams, R&D labs, regulatory agenciesManufacturing facilities, quality assurance labs, regulatory bodies
Employer & Industry UsageMedical device manufacturers, software firms in healthcareMedical device manufacturers, healthcare companies, regulatory agencies
Common Search & ComparisonFocuses on software development and complianceFocuses on quality processes and regulatory adherence

Medical Device Software professionals develop and maintain software used in medical devices, ensuring functionality and compliance. Medical Device Quality Assurance Specialists focus on testing, validation, and ensuring products meet quality standards. Both roles are essential in the medical device industry but differ in their core responsibilities and skill sets.

Can I make 200k a year as a software engineer?

Medical device software engineers can potentially earn $200,000 or more annually, especially with experience, specialized skills in embedded systems or regulatory compliance, and working in high-paying regions or companies. Salaries vary based on location, level of expertise, certifications, and the complexity of the projects involved.

What are some common challenges faced by professionals working in Medical Device Software development?

Professionals in Medical Device Software development often navigate complex regulatory requirements, such as FDA or ISO standards, which can impact project timelines and processes. Collaborating closely with cross-functional teams—including hardware engineers, clinicians, and quality assurance specialists—is essential to ensure safety and compliance. Additionally, balancing innovation with rigorous documentation and validation can be challenging, as even minor software changes may require extensive testing and approval. Staying updated with evolving cybersecurity standards is also a key part of the role.

Will AI replace medical device sales jobs?

AI is unlikely to fully replace medical device sales jobs, as these roles require relationship-building, technical knowledge, and understanding customer needs. AI can assist with data analysis, product information, and automating routine tasks, but human interaction remains essential for sales success in this field. Sales professionals may need to adapt by integrating AI tools into their workflows to enhance efficiency and customer engagement.

What engineer makes $500,000 a year?

In the field of medical device software, senior engineers with extensive experience, specialized skills, and leadership roles can earn salaries approaching or exceeding $500,000 annually, especially in high-cost regions or with bonuses and stock options. Such compensation typically requires advanced certifications, a strong track record, and often managerial responsibilities.

What is medical device software?

Medical device software is specialized software designed to be used for medical purposes, such as diagnosing, preventing, monitoring, or treating health conditions. It can be embedded within a medical device (like a pacemaker) or function as standalone software (such as mobile health apps). This software must comply with strict regulatory standards to ensure safety and effectiveness, as it directly impacts patient health and safety. Developers of medical device software must follow guidelines from authorities like the FDA or EU MDR, depending on the market. Regular updates, risk management, and comprehensive testing are also essential parts of its development process.
More about Medical Device Software jobs
What cities are hiring for Medical Device Software jobs? Cities with the most Medical Device Software job openings:
What states have the most Medical Device Software jobs? States with the most job openings for Medical Device Software jobs include:
What job categories do people searching Medical Device Software jobs look for? The top searched job categories for Medical Device Software jobs are:
Medical Device Software jobs near you
Infographic showing various Medical Device Software job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 88% Full Time, 2% Part Time, and 9% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Senior Software Engineer

Cesna Recruitment

San Diego, CA

$130K - $171K/yr

Full-time

Posted 17 days ago

Job description

[Position]

Senior Software Engineer

[About Our Client]

Research & Development hub for artificial intelligence and deep learning technologies and is also home to a dedicated medical device software team focused on the development of advanced, safety-critical healthcare solutions.

[Job Summary]

We are seeking a Senior Software Engineer to play a key role in maintaining, evolving, and selectively developing our Ez-X medical X-ray imaging system.

This role primarily focuses on maintaining and stabilizing the existing C++ software platform, supporting the C# GUI architecture, and implementing business logic at the platform level. In addition, the role includes re-implementing and adapting existing business logic using a newly developed internal software platform, ensuring functional equivalence, system stability, and seamless integration.

While new feature development is part of the role, a significant portion of the work involves long-term platform maintenance, system optimization, and system-level integration across imaging algorithms, control systems, and X-ray hardware.

As medical device development is iterative and subject to regulatory, technical, and business considerations, specific responsibilities, priorities, and technical focus areas may evolve over time, provided they remain aligned with the scope and seniority of this role.

You will act as a technical leader within the software team and collaborate closely with Vision, Control, Mechanica, Platform, and X-Ray hardware teams.

[Job Description]

The responsibilities listed below describe the primary functions of this role but are not intended to be an exhaustive list. Additional responsibilities may be assigned as needed, provided they are consistent with the employee's role, expertise, and professional experience.

- Design, implement, and maintain C++ software platform components and shared interface libraries

- Architect and develop C# GUI frameworks supporting end-to-end medical imaging and clinical workflows

- Act as a technical lead for a team, aligning system requirements, architecture, and development priorities in close collaboration with the software group leader

- Serve as the technical bridge across software, hardware, and research teams, leading design reviews and driving key architectural and technical decisions

- Support software verification, validation, and documentation activities for regulatory submissions, collaborating closely with QA and regulatory teams during FDA submissions and audits

- Mentor junior engineers, conduct code reviews, and promote best practices in software development

Requirements

Required Qualifications

- Bachelor's in Computer Science, Software Engineering, or equivalent

- 5+ years of professional software development experience

- Strong proficiency in modern C++

- Experience with C# GUI development

- Solid understanding of multi-threading, synchronization, and performance optimization

- Able to work in US without any Work Visa sponsor/transfer/Extension/ support, now and future

Preferred Qualifications

- Master's degree in Computer Science, Software Engineering, or equivalent

- Experience designing software architectures for complex systems

- Prior experience in medical device software development

- Knowledge of FDA regulations, IEC 62304, ISO 14971

- Experience with medical imaging, DRR, CT, or X-ray systems

- Experience with real-time or near-real-time systems

- Familiarity with software safety classification and risk management

- Experience supporting FDA submissions or audits

- Bilingual in English and Korea would be a plus

Benefits

[What's On Offer]

- Key technical role in next-generation medical X-ray systems

- Direct impact on FDA-regulated medical products

- Leadership opportunities in a growing US medical device team

- Competitive salary and benefits (US market)

- Long-term stability and global product exposure

Apply