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Medical Device Software Engineer Jobs in California

Cesna Recruitment

Senior Software Engineer

San Diego, CA · On-site

$130K - $171K/yr

As medical device development is iterative and subject to regulatory, technical, and business ... Software Engineering, or equivalent - 5+ years of professional software development experience ...

Diality

Director, Software Engineering

Irvine, CA · Hybrid

$223K - $260K/yr

... software engineer contractors. * Familiarity with cloud-connected medical device systems, mobile applications, interoperability, healthcare data platforms, and device-to-cloud communication ...

Diality Inc

Director, Software Engineering

Irvine, CA · On-site

$223K - $260K/yr

... software engineer contractors. * Familiarity with cloud-connected medical device systems, mobile applications, interoperability, healthcare data platforms, and device-to-cloud communication ...

Diality

Director, Software Engineering (Irvine)

Irvine, CA · On-site

$270K/yr

The Director of Software Engineering is responsible for establishing software engineering strategy ... engineer contractors. * Familiarity with cloud‑connected medical device systems, mobile ...

IT America Inc

Staff Software Engineer

Hercules, CA · On-site

Staff Software Engineer Location: Hercules, California Duration: Long term contract As a Staff ... Background in laboratory equipment, clinical diagnostics, or medical device development.

Rangam Consultants

Software Engineer

San Diego, CA · On-site

Support compliance considerations related to regulated medical device software development practices. * Document findings and recommendations to facilitate efficient handoff to permanent engineering ...

Alcon

Principal, Software Engineer

Lake Forest, CA · On-site

$143K - $192K/yr

The Principal Software Engineer, Medical Device Systems is responsible for maintaining, enhancing, and supporting software for Alcon's on-market ophthalmic medical devices and imaging platforms. This ...

Abbott

Software Quality Engineer

Alameda, CA · On-site

$80 - $85/hr

Review quality system documentation products as they apply to the development, verification, validation, use, and maintenance of medical device software. Coordinate activities with other engineering ...

Cesna Group

Senior Software Engineer

San Diego, CA · On-site

$100K - $200K/yr

We are seeking a Senior Software Engineer to play a key role in maintaining, evolving, and ... As medical device development is iterative and subject to regulatory, technical, and business ...

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All JobsMedical Device Software Engineer JobsMedical Device Software Engineer Jobs in California

Medical Device Software Engineer information

See California salary details

$62.7K

$145.6K

$202.8K

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

As of Aug 22, 2026, the average yearly pay for medical device software engineer in California is $145,592.00, according to ZipRecruiter salary data. Most workers in this role earn between $118,400.00 and $170,700.00 per year, depending on experience, location, and employer.

What is a medical device software engineer?

A Medical Device Software Engineer is responsible for designing, developing, testing, and maintaining software used in medical devices. They ensure compliance with regulatory standards like FDA and IEC 62304 while working on embedded systems, user interfaces, or cloud-based healthcare applications. Their role involves collaborating with cross-functional teams, including hardware engineers and regulatory specialists, to ensure patient safety and product effectiveness.

What are the typical daily responsibilities of a medical device software engineer?

Medical Device Software Engineers typically spend their days designing, coding, and testing software for medical devices in compliance with health regulations. They collaborate closely with hardware engineers, quality assurance teams, and regulatory specialists to ensure that the software integrates seamlessly with device hardware and meets performance and safety standards. Documenting development processes, participating in code reviews, and addressing feedback from cross-functional teams are also common aspects of the role. This position often requires troubleshooting issues in both simulated and real clinical environments to ensure the reliability and safety of the device.

What are the key skills and qualifications needed to thrive as a medical device software engineer?

To thrive as a Medical Device Software Engineer, you need a solid background in software development, embedded systems, and biomedical engineering, often supported by a degree in computer science, electrical engineering, or a related field. Experience with programming languages like C/C++, knowledge of real-time operating systems, and familiarity with medical device regulatory standards such as IEC 62304 are typically required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for this position. These skills ensure high-quality, compliant software that contributes to safe and reliable medical devices, which are critical for patient health.

What are the most commonly searched types of Medical Device Software Engineer jobs in California?

The most popular types of Medical Device Software Engineer jobs in California are:

What are popular job titles related to Medical Device Software Engineer jobs in California?

For Medical Device Software Engineer jobs in California, the most frequently searched job titles are:

What job categories do people searching Medical Device Software Engineer jobs in California look for?

The top searched job categories for Medical Device Software Engineer jobs in California are:

What cities in California are hiring for Medical Device Software Engineer jobs?

Cities in California with the most Medical Device Software Engineer job openings:

Medical Device Software Engineer jobs near you
Infographic showing various Medical Device Software Engineer job openings in California as of August 2026, with employment types broken down into 77% Full Time, 3% Temporary, and 20% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $145,592 per year, or $70 per hour.

Software Design Control Engineer

Jobtailor

San Francisco, CA • On-site

$130 - $190/hr

Other

Posted 4 days ago

Job description

  • Work alongside software engineers to author, review, and maintain comprehensive design control documentation, including Software Requirements Specifications, Architecture & Design Documents, and Traceability Matrices.
  • Ensure software development processes align with IEC 62304 (Medical Device Software Lifecycle), ISO 13485, and FDA 21 CFR Part 820 regulations.
  • Author and maintain software risk management files, including Software FMEAs per ISO 14971.
  • Produce software verification and validation (V&V) protocols and reports in coordination with the engineering and test teams to ensure full traceability.
  • Compile and organize necessary software technical documentation for regulatory submissions.
  • Maintain and update software documentation for post-market surveillance, CAPAs, and software updates.
Requirements
  • 5+ years of experience in the medical device industry, specifically working with software‑driven or connected medical devices (Class II or Class III).
  • A Bachelor’s degree in Computer Science, Biomedical Engineering, Software Engineering, or a related field, or equivalent practical engineering experience.
  • Demonstrated experience writing, reviewing, and managing formal medical device software documentation (Design History Files, Traceability Matrices).
  • Proven track record of taking a medical device software product through a successful FDA clearance/approval process and subsequent launch.
  • Deep familiarity with IEC 62304, ISO 14971, and FDA Software Validation Guidelines.
  • Experience with modern software development workflows (e.g. Git, Jira) and quality system tools (e.g. Greenlight Guru, Arena, Matrix Requirements, or Jama).
Core Competencies

Expertise in authoring and managing medical device software documentation, including compliance with IEC 62304, ISO 14971, and FDA regulations. Proven ability to navigate the FDA clearance process for software‑driven medical devices.

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