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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 ...

PrideStaff

Assembly Tech - Medical Device

San Clemente, CA · On-site

$21 - $22/hr

Use basic computer software during production processes Qualifications * High school diploma or equivalent * Manufacturing, production, assembly, electronics assembly, or medical device experience ...

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Medical Device Software information

See California salary details

$21

$49

$95

How much do medical device software jobs pay per hour?

As of Aug 16, 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 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 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.

Is medical device software a good career?

Medical device software is a growing field that involves developing and maintaining software for medical equipment, requiring knowledge of regulatory standards like FDA and ISO. It offers opportunities in healthcare technology, often requiring skills in programming, testing, and compliance, with a stable job outlook due to increasing healthcare needs. Professionals in this area can work in multidisciplinary teams and may need certifications such as ISO 13485 or IEC 62304.

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 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 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, 77% Full Time, 15% Part Time, 2% Temporary, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $102,304 per year, or $49.2 per hour.

W2 Software Project Lead

Kanak Elite Services Inc

California Hot Springs, CA • On-site

Contractor

Posted 10 days ago

Job description

Our Client is hiring for Software Project Lead for a 12 months contract role on renewable basis. Its a Hybrid role in Valencia, CA. 

Need Local- Visa Independent Candidate

Software Project Lead
About the role:
This role serves as the primary owner for software activities, aligning technical execution with business objectives, regulatory expectations, and product roadmaps.
As a key member of the Software group and is critical to accelerating innovation through acquisition while maintaining patient safety, regulatory compliance, and software quality. The Software Project Lead ensures that acquired software technologies are seamlessly and responsibly integrated into the medical device portfolio—turning strategic investments into safe, effective products for patients.
Work Mode -  We value collaboration and synergy. This role follows a hybrid work model, requiring employees to be in our local office at least three days per week.
Responsibilities:
• Leading the planning and execution of complex software development and integration software.
• Partnering closely with R&D, Quality, Regulatory, IT, Cybersecurity, Clinical, Operations and other cross-functional teams to develop software solution into the company’s medical device portfolio while ensuring compliance with global regulatory standards and internal quality systems.
• Develop and maintain plans covering software development, verification/validation, cybersecurity, and regulatory deliverables.
• Manage program schedules, budgets, resources, risks, and interdependencies across multiple cross functional teams.
• Provide clear, data driven program status, risks, and decision points to R&D leadership.
• Drive alignment between legacy and acquired development processes, tools, architectures, and documentation.
• Work closely with software engineering teams to ensure development and integration activities comply with applicable standards.
• Ensure proper integration of software lifecycle artifacts, including requirements, architecture, risk management, verification, validation, and cybersecurity documentation.
• Support design reviews, phase gate reviews, and regulatory submissions related to integrated software products.
• Facilitate alignment on system architectures, interfaces, data flows, and platform strategies across organizations.
• Drive issue resolution and decision making across organizational boundaries.
• Track software project progress and provide transparent communication and interfaces with all areas affected by the project including cross-functional stakeholders, business sponsors, and senior management.
• Conduct retrospectives, and lessons learned, and implement process improvement initiatives to drive future success.
• Additional duties, as assigned.
Key Competencies and Capabilities
• Ability to plan and execute software projects in the medical device industry, with preferred experience in medical device software, including new product development and sustaining software.
• Working knowledge of the software development lifecycle (SDLC) in a regulated environment, with exposure to agile or hybrid delivery models.
• Proficiency with project management and software delivery tools (e.g., MS Project, JIRA), including development of WBS, schedules, and dependency tracking.
• Working understanding of software day to day challenges and system level integration, sufficient to support cross functional execution.
• Strong verbal and written communication skills, with the ability to collaborate across Software, Systems, Quality, and Regulatory teams and drive on time delivery.
• Demonstrated organizational and problem solving skills, with the ability to manage assigned scope and operate effectively within a regulated, quality driven environment.
Required Qualifications:
• Bachelor’s degree in engineering, Computer Science, or related technical discipline.
• Software Development experience 5 years minimum C#, WPF Minimum 5 yrs.. hands on development experience
• Web technology Experience 2 yrs preferred
• 10-15 years of experience in software project management within software driven medical devices or other regulated industries.
• Demonstrated experience leading cross functional software development programs.
• Strong understanding of regulated software development lifecycles and quality systems.
• Proven ability to manage complex, ambiguous programs with multiple stakeholders.
Preferred Qualifications:
• Familiarity with FDA, EU MDR, and global regulatory expectations for software enabled medical devices.
• Experience with cybersecurity, cloud connected devices.
• PMP, PgMP, Agile, or SAFe certification.
• Master’s degree in Engineering, Management, or related field.


Thanks & Regards,

Recruitment Manager

Ravi Pratap

Email : Recruiters@kanakits.com

Kanak IT Services LLC.|| Hamilton Square, NJ 08690

Website : www.kanakits.com