1

Medical Device Software Testing Jobs in California

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.75/hr

... Device Assembler, you will ... Perform assembly, repair, and testing of medical catheters under close supervision in a regulated ...

Your work in assembling, soldering, and testing these devices ensures high-quality, reliable medical solutions that help improve patient outcomes worldwide. Job Title: Medical Device Assembler Pay ...

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.67/hr

... Device Assembler, you will ... Perform assembly, repair, and testing of medical catheters under close supervision in a regulated ...

Be Seen First

... testing, verification, and troubleshooting activities • Maintain a clean and organized work area Qualifications: • Experience in medical device assembly, electronics assembly, cleanroom ...

Experience testing Software as a Medical Device (SaMD) or other regulated medical device software preferred; strong candidates from other regulated or quality-critical environments will also be ...

Showing results 41-60

Medical Device Software Testing information

See California salary details

$18

$42

$69

How much do medical device software testing jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for medical device software testing in California is $42.94, according to ZipRecruiter salary data. Most workers in this role earn between $32.98 and $51.73 per hour, depending on experience, location, and employer.

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

AspectMedical Device Software TestingMedical Device Quality Assurance
CertificationsISTQB, CSTE, or similar testing certificationsISO 13485, CAPA, or quality management certifications
Work EnvironmentTesting labs, development teams, regulated environmentsQuality management systems, compliance departments
Employer & Industry UsageMedical device companies, software developersManufacturers, regulatory agencies, compliance firms
Search & Comparison IntentUnderstanding testing roles, skills, and responsibilitiesUnderstanding quality assurance processes, compliance standards

Medical Device Software Testing focuses on verifying and validating software functionalities to ensure safety and compliance. Medical Device Quality Assurance encompasses broader quality management practices, including process audits and compliance to standards. Both roles are essential in the medical device industry but serve different purposes in ensuring product safety and regulatory adherence.

What is medical device software testing?

Medical device software testing is the process of verifying and validating the software used in medical devices to ensure it is safe, reliable, and compliant with regulatory standards. This involves various testing methods, such as functional, performance, and usability testing, to identify and fix potential issues before the device is released to the market. Proper software testing helps prevent device failures that could harm patients and ensures that the device operates as intended under all expected conditions.

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

To excel as a Medical Device Software Tester, you need a strong background in software testing methodologies, knowledge of regulatory standards like IEC 62304, and a degree in computer science or engineering. Familiarity with testing tools such as Selenium, Jira, and automated test frameworks, as well as experience with validation and verification documentation, is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills that help testers identify issues and collaborate with cross-functional teams. These skills and qualifications are vital to ensure the safety, reliability, and compliance of medical device software in a highly regulated industry.

What are some common challenges faced by professionals in medical device software testing, and how can they be addressed?

Professionals in medical device software testing often encounter challenges such as ensuring compliance with strict regulatory standards (like FDA or ISO 13485), managing complex documentation requirements, and keeping up with frequent software updates. Addressing these challenges requires a strong focus on detail, thorough understanding of relevant regulations, and effective communication with development and quality assurance teams. Collaborating closely with cross-functional teams and maintaining up-to-date knowledge of regulatory changes are key to successfully navigating these demands.
What job categories do people searching Medical Device Software Testing jobs in California look for? The top searched job categories for Medical Device Software Testing jobs in California are:
Infographic showing various Medical Device Software Testing job openings in California as of July 2026, with employment types broken down into 78% Full Time, 14% Part Time, and 8% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $89,305 per year, or $42.9 per hour.
Senior Software Quality Engineer, Product/Software Cybersecurity (Medical Device Software)

Senior Software Quality Engineer, Product/Software Cybersecurity (Medical Device Software)

Edwards Lifesciences Corporation

Irvine, CA

$108K - $153K/yr

Full-time

Posted 12 days ago


Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

68th of 535 rated manufacturers


Job description

Imagine how your ideas and expertise can change a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You'll bring your passion for problem solving and partner with various teams to influence decision-making for a product's entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.

The Senior Software Quality Engineer is a key member of the Software Quality organization, responsible for ensuring the cybersecurity of product software including Software as a Medical Device (SaMD), Software in a Medical Device (SiMD), software as an accessory to a medical device, and other Digital Health Technologies. This role is responsible for owning and advancing product cybersecurity processes established within our Quality Management System and ensure alignment with applicable regulatory standards and industry guidance. The position will work in close partnership with R&D, Product Security, Quality and other cross-functional team members to integrate cybersecurity requirements throughout the product software development lifecycle and support effective postmarket cybersecurity management.

We are seeking an ambitious, technically strong candidate with a solid foundation in quality and cybersecurity, excellent communication skills, and the ability to build trusted relationships across the organization. This role offers meaningful opportunities to grow within a dynamic and evolving Software Quality function.

How you will make an impact:

  • Own the establishment, implementation, and continuous improvement of cybersecurity related processes for product software established in our Quality Management System
  • Review and approve product cybersecurity related deliverables across the lifecycle, including planning, requirements, architecture/design, risk management, verification and validation, and problem resolution (dispositioning of cybersecurity vulnerabilities and defects).
  • Execute Cybersecurity risk analysis on our products.
  • Provide assurance that all requirements related to cybersecurity are followed when developing or making changes to product software.
  • Work in close partnership with Product Security, Quality and R&D to address and monitor cybersecurity risks throughout the Product Software Development Lifecycle.
  • Support regulatory submissions and responses regarding cybersecurity related requests.
  • Effectively manage multiple priorities, projects and ability to communicate at all levels of personnel.
  • Author, review and approve documents in our Application Lifecycle Management and Product Lifecycle Management systems.
  • Willingness to work in a fast-paced, dynamic environment to meet the needs of the business and deliver safe quality products to our patients.

What you will need (Required):

  • Bachelor's degree in Scientific, Engineering, or Computer Sciencefields plus four (4) years of relevant work experience; OR Master's degree Scientific, Engineering, or Computer Sciencefields plus two (2) years of relevant work experience; or equivalent work experience based on Edwards criteria .
  • Highly regulated industry experience
  • Experience with software development and/or software quality in regulated environments

What else we look for (Preferred):

  • Engineering or Computer Science degree
  • Medical device industry experience
  • Experience with cybersecurity risk assessments
  • Experience integrating cybersecurity into the SDLC / design controls
  • Familiarity with vulnerability management and post market cybersecurity processes
  • Familiarity withsoftware(IEC 62304) and cybersecurity (NIST)guidelines; includingunderstanding ofWaterfall and Agile conceptsin context with the SDLC process.
  • Knowledge and experience in Medical Device Risk Management (ISO 14971)
  • Excellent written and verbal communication skillsrequired.

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $108,000 to $153,000 in tool (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

COVID Vaccination Requirement

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.


What Edwards Lifesciences employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Edwards Lifesciences logo

About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958