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Medical Device Software Engineer Jobs in California

Senior Quality Engineer

Redwood City, CA · On-site

$108K - $146K/yr

S. or higher preferred in Computer Science, Software Engineering, Informatics, Biomedical, or relevant engineering disciplines. • 5+ years experience in FDA regulated domain (e.g. medical device ...

As a Senior Quality Engineer , you will: * Lead verification, validation and maintenance of host ... Be involved in the medical device software design controls activities, in accordance with the FDA ...

Medical Device Engineer Support the development, validation, and optimization of electrochemical test methods used for next-generation medical monitoring technologies. Partner with engineers to ...

This person will monitor design controls that govern the development, verification, validation, use, and maintenance of medical device software. The Software Compliance Engineer will also coordinate ...

This person will monitor design controls that govern the development, verification, validation, use, and maintenance of medical device software. The Software Compliance Engineer will also coordinate ...

This person will monitor design controls that govern the development, verification, validation, use, and maintenance of medical device software. The Software Compliance Engineer will also coordinate ...

This person will monitor design controls that govern the development, verification, validation, use, and maintenance of medical device software. The Software Compliance Engineer will also coordinate ...

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Showing results 1-20

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 Jul 16, 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 are the key skills and qualifications needed to thrive in the Medical Device Software Engineer position, and why are they important?

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 is a Medical Device Software Engineer job?

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 some 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 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 cities in California are hiring for Medical Device Software Engineer jobs? Cities in California with the most Medical Device Software Engineer job openings:
Infographic showing various Medical Device Software Engineer job openings in California as of July 2026, with employment types broken down into 5% Internship, 60% Full Time, 5% Temporary, and 30% Contract. Highlights an 100% In-person job distribution, with an average salary of $145,592 per year, or $70 per hour.
Sr. Software Quality Engineer

Full-time

Re-posted 14 days ago


BD rating

7.3

Company rating: 7.3 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

265th of 430 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Job Summary
As a Sr. Software Quality Engineer at Becton, Dickinson and Company, you will play a critical role in ensuring the quality and reliability of our medical device software. You will be responsible for defining, implementing, and executing robust quality assurance processes throughout the entire software development lifecycle, contributing to the delivery of safe and effective products that positively impact patient care.

Job Responsibilities

  • Develop, implement, and maintain comprehensive software quality assurance strategies, plans, and procedures in accordance with industry best practices and regulatory requirements (e.g., FDA, ISO 13485, IEC 62304).

  • Experience in being lead SWQA for new product development projects.

  • Ability to understand software risks and develop risk management files for software and system level risk.

  • Lead defect management and CCB meetings to review and disposition project defects

  • Lead and participate in design reviews, code reviews, and other technical assessments to identify potential quality issues early in the development process.

  • Understanding of test plans, test cases, and test scripts for various levels of testing, including unit, integration, system, and regression testing.

  • Perform risk analysis and develop mitigation strategies for software defects and quality-related issues.

  • Understanding of complaints process and metrics

  • Collaborate closely with software development, project management, and regulatory affairs teams to ensure seamless integration of quality activities throughout the product lifecycle.

  • Investigate, analyze, and document software defects, working with development teams to ensure timely resolution and verification.

  • Contribute to the continuous improvement of software development processes and quality assurance methodologies.

  • Participate in external and internal audits, providing documentation and expertise related to software quality.

  • Stay current with emerging technologies, industry trends, and regulatory changes in medical device software quality.


Job Qualifications

  • Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or a related technical field. Master's degree preferred.

  • 5+ years of experience in software quality assurance, with at least 2 years in the medical device industry or another highly regulated environment.

  • Strong understanding of software development lifecycle (SDLC) methodologies (e.g., Agile, Waterfall) and their application in a regulated context.

  • In-depth knowledge of relevant medical device regulations and standards, including FDA 21 CFR Part 820 (QSR), ISO 13485, and IEC 62304.

  • Proven experience in designing, implementing, and executing various types of software testing.

  • Proficiency with test management tools (e.g., Polarion, Jira, Azure DevOps) and defect tracking systems. Polarion knowledge is a plus.

  • Experience with automated testing frameworks and tools (e.g., Selenium, Coded UI, Squish) is highly desirable.

  • Excellent analytical, problem-solving, and critical thinking skills.

  • Strong communication (written and verbal) and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.

  • Ability to work independently and as part of a team in a fast-paced, dynamic environment.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

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Primary Work LocationUSA CA - Irvine Laguna CanyonAdditional LocationsWork Shift

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

$105,500.00 - $168,800.00 USD Annual

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About BD

Sourced by ZipRecruiter

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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