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Medical Device Software Jobs in California (NOW HIRING)

Epia Neuro

Staff Software Engineer

Alameda, CA · On-site

The Role We're looking for a Staff Software Engineer to lead our clinician-facing and patient ... Experience with a medical-grade device-management platform. * Human factors / usability engineering ...

Kelly Services

Medical Device Technician

Irvine, CA

$30/hr

... system software upgrades on ULS sims, carto laptop sims & workstations systems - Maintain all ... Apply to be an Medical Device Technician today! #GRACE As part of our promise to talent, Kelly ...

Socket.dev

Software V&V Engineer

Milpitas, CA · On-site

$95 - $110/hr

Experience with medical device software, or Software as a Medical Device * Familiarity with ... applicable standards and regulations such as IEC 62304, ISO 13485, ISO 14971, FDA design controls ...

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Medical Device Software information

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$21

$49

$95

How much do medical device software jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for medical device software in California is $49.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $58.85 per hour, depending on experience, location, and employer.

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.

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 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 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.

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.

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

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

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

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

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

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

Medical Device Software jobs near you
Infographic showing various Medical Device Software job openings in California as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $102,304 per year, or $49.2 per hour.

Principal Software Engineer - Mobile Development

Boston Scientific

San Jose, CA • On-site

$150 - $190/hr

Other

Re-posted 13 hours ago

Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Location(s)

US-CA-Santa Clara; US-CA-San Jose; US-CA-Valencia

About the role

The Principal Software Engineer – Mobile Applications will serve as a technical leader and hands‑on developer responsible for designing, developing, and maintaining advanced Android and cross‑platform mobile applications. This role blends technical expertise with team leadership, ensuring delivery of secure, high‑quality, and compliant medical software solutions in accordance with FDA and ISO 13485 standards.

Responsibilities
  • Lead the architecture, design, and development of mobile applications for implantable medical devices using Kotlin Multiplatform and Core Java.
  • Ensure secure communication between devices and cloud systems via Bluetooth Low Energy (BLE) and AWS-based APIs.
  • Develop and maintain libraries and SDKs for cross‑platform mobile applications.
  • Integrate mobile applications with AWS cloud infrastructure (KMS, S3, DynamoDB, Cognito, API Gateway, EC2, CloudWatch).
  • Author and review key design documentation: architecture specs, DFMEA, cybersecurity reports, threat models, etc.
  • Conduct peer reviews and maintain code integrity, ensuring traceability and compliance per medical device process.
  • Lead Agile/Scrum ceremonies, mentoring distributed teams (U.S., Costa Rica, India, China, Ukraine) across time zones.
  • Estimate timelines, propose plans, review milestones and lead app development from concept through commercialization.
Required qualifications
  • Bachelor’s or Master’s degree in Computer science, Software Engineering, or related field.
  • 8+ years of experience in Android mobile app development, with at least 2+ years in medical device application.
  • Experience of architecting, designing and developing mobile applications.
  • Strong command of at least three of the following technologies and frameworks: Kotlin, Kotlin Multiplatform, Java, and Android Jetpack architectures, including MVVM, Rx, and XML data binding.
  • 3+ years’ experience with AWS services and secure communication protocols (BLE, Wi‑Fi, HTTPS, OAuth).
  • Good understanding of IEC 62304, ISO 13485, and FDA design controls for medical device software.
  • Excellent communication skills with the ability to collaborate across global teams, lead cross‑functional projects, and develop documentation supporting regulatory deliverables.
Preferred qualifications
  • Experience in Developing Mobile apps for Neuromodulation devices.
  • Experience with CI/CD (Jenkins, Git), SonarQube, and Atlassian Agile tools.
  • Prior experience on secure BLE communication, data encryption, and integration with AWS cloud services (S3, DynamoDB, Cognito, API Gateway).
  • Experience in cybersecurity techniques (sandboxing, code obfuscation, penetration testing).
  • Exposure to data science or machine learning frameworks (TensorFlow, Pandas, NumPy, R).
EEO Statement

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

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About Boston Scientific

Sourced by ZipRecruiter

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.

Industry

Medical equipment and supplies manufacturing, manufacturing and construction

Company size

10,000+ Employees

Headquarters location

Marlborough, MA, US

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