1

Medical Device Software Engineer Jobs in Texas (NOW HIRING)

Spectral AI, Inc. (Spectral) is seeking a software engineer to join our growing design and ... Experience in medical device software development * Familiarity with regulated software ...

Spectral AI, Inc. (Spectral) is seeking a software engineer to join our growing design and ... Experience in medical device software development * Familiarity with regulated software ...

The Cyber Security Engineer will support the design, development, and maintenance of secure medical device software systems, ensuring that cybersecurity controls are resilient and compliant with FDA ...

Familiarity with IEC 62304 (Medical Device Software Lifecycle Processes) * Familiarity with FDA ... Software Design Controls Engineer * Software Quality * Regulated software development Expected ...

... regulated medical device software. These systems will support the full software lifecycle, from ... Partner closely with software engineering teams to embed: * Compliance with CI/CD pipelines

Produce software validation packages for both medical and non-medical device software * Review and approve supplier documentation as needed * Review and approve specifications as needed * Create ...

... Engineer to follow up on features & defects • Ability to travel is required • Verify all software systems comply US FDA's 21 CFR Part 820 (QMSR) and IEC 62304 (Medical Device Software Lifecycle ...

Senior Embedded Software Engineer

Irving, TX

$119K - $156K/yr

Production medical device software with strict quality and traceability needs Your Impact * Design ... Engineering culture focused on disciplined design, testing, and quality * Direct impact on medical ...

Senior Embedded Software Engineer

Irving, TX · On-site

$119K - $156K/yr

Production medical device software with strict quality and traceability needs Your Impact * Design ... Engineering culture focused on disciplined design, testing, and quality * Direct impact on medical ...

Senior Embedded Software Engineer

Irving, TX · On-site

$119K - $156K/yr

Production medical device software with strict quality and traceability needs Your Impact * Design ... Engineering culture focused on disciplined design, testing, and quality * Direct impact on medical ...

... Engineer to follow up on features & defects Ability to travel is required * Verify all software systems comply US FDA's 21 CFR Part 820 (QMSR) and IEC 62304 (Medical Device Software Lifecycle ...

next page

Showing results 1-20

Medical Device Software Engineer information

See Texas salary details

$59.2K

$137.4K

$191.5K

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

As of Jun 16, 2026, the average yearly pay for medical device software engineer in Texas is $137,441.00, according to ZipRecruiter salary data. Most workers in this role earn between $111,800.00 and $161,200.00 per year, depending on experience, location, and employer.

Who is eligible for Medi-Cal?

Medi-Cal is California's Medicaid program, providing health coverage to low-income individuals and families, including pregnant women, seniors, persons with disabilities, and those meeting income and asset requirements. Eligibility depends on income level, household size, and specific circumstances, and applicants often need to provide proof of income and residency. Medical device software engineers should verify their eligibility if seeking coverage for health-related needs or benefits related to employment.

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 does medical mean?

In the context of a Medical Device Software Engineer, 'medical' refers to products, devices, or software used for healthcare purposes, such as diagnosis, treatment, or monitoring of patients. These products are regulated to ensure safety and effectiveness and often require compliance with standards like FDA or ISO. The role involves developing software that meets strict quality and safety requirements specific to healthcare environments.

Is Medi-Cal the same as Medicaid?

Medical Device Software Engineers should understand that Medi-Cal and Medicaid are related but not identical; Medi-Cal is California's Medicaid program, which provides health coverage to low-income residents, while Medicaid is a federal and state program serving similar purposes across the U.S. Differences may include specific benefits, eligibility criteria, and administration. Knowledge of healthcare policies can be important when developing compliant medical software for different regions.

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's the difference between Medicare and Medi-Cal?

Medicare is a federal health insurance program primarily for people aged 65 and older or with certain disabilities, while Medi-Cal is California's Medicaid program providing free or low-cost health coverage for low-income individuals. As a Medical Device Software Engineer, understanding these programs can be relevant when designing compliant healthcare software and ensuring accessibility for diverse patient populations.
What are the most commonly searched types of Medical Device Software Engineer jobs in Texas? The most popular types of Medical Device Software Engineer jobs in Texas are:
What are popular job titles related to Medical Device Software Engineer jobs in Texas? For Medical Device Software Engineer jobs in Texas, the most frequently searched job titles are:
What cities in Texas are hiring for Medical Device Software Engineer jobs? Cities in Texas with the most Medical Device Software Engineer job openings:
Principal Software Quality Assurance Engineer (Remote - United States)

Principal Software Quality Assurance Engineer (Remote - United States)

Healthcare

San Antonio, TX

$121K - $163K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 days ago


Job description

Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers' toughest challenges. While we continue updating the Solventum Careers Page and applicant materials, some documents may still reflect legacy branding. Please note that all listed roles are Solventum positions, and our Privacy Policy: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ applies to any personal information you submit. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Job Description:

Principal Software Quality Assurance Engineer

3M Health Care is now Solventum

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.

We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.

The Impact You'll Make in this Role

As a Principal Software Quality Assurance Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:

  • Leading software assurance activities throughout medical device software life cycle, including creating software quality assurance plan, determining software safety classification, software test readiness, software release readiness. Responsible for ensuring traceability upwards to system level requirements and safety/security risk controls as well as downwards to software design, implementation and testing.
  • Being an active member of the software team during the whole software life cycle, with responsibility for physical and functional configuration audits, reviewing and approving software requirements, software architectural and detailed design, test procedures, test logs, test results, and providing insight to management regarding software project status and software quality metrics.
  • Ensuring compliance with applicable regulatory requirements and industry standards; performing gap assessments; immediately elevating to management any major problem with device software that could affect patient safety, cyber security, customer usability or system adherence to process requirements
  • Acting as a quality champion in software product development and testing teams
  • Supporting other software related processes such as CAPA process, and other quality related processes regarding cybersecurity risk management and software quality assurance.

Your Skills and Expertise

To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:

  • Master's degree or higher in Computer Science, Software Engineering, Computer Engineering, Electrical Engineering, Cyber Security, or Information Science (completed and verified prior to start) and five (5) years of experience in software quality assurance in medical device, aerospace, or automotive industry

OR

  • Bachelor's degree in Computer Science, Software Engineering, Computer Engineering, Electrical Engineering, Cyber Security or Information Science (completed and verified prior to start) and seven (7) years of experience in software quality assurance in medical device, aerospace, or automotive industry

Additional qualifications that could help you succeed even further in this role include:

  • Working knowledge of premarket and postmarket medical device regulations (FDA, EU and other agencies), as well as medical device related standards, such as ISO 13485, ISO 14971, IEC 62304, IEC 81001-5 series amongst others.
  • Experience developing and testing software systems, SaMD, SiMD, and/or embedded software and creating appropriate documentation
  • Knowledge of Software Engineering best practices and working knowledge of C language preferred
  • Experience with embedded systems, IoT, Bluetooth, wi-fi and cellular technologies
  • Excellent verbal and written communication skills, strong problem-solving ability, and attention to detail
  • Ability to effectively manage multiple simultaneous tasks and priorities and perform under a dynamic environment with parallel product releases and multiple project teams
  • Ability to deal effectively with other employees and external business contacts while conveying a positive, service-oriented attitude.

Work location:

  • Remote in United States (preferred near Eagan, MN or San Antonio, TX area)

Travel: May include up to 5% domestic/international

Relocation Assistance: May be authorized

Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).

Supporting Your Well-being

Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.

Applicable to US Applicants Only:The expected compensation range for this position is $124,000 - $170,500, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: https://www.solventum.com/en-us/home/our-company/careers/#Total-RewardsResponsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.

Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.

Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain of @solventum.com. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.

Please note, Solventum does not expect candidates in this position to perform work in the unincorporated areas of Los Angeles County.Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.

Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.

Solventum Global Terms of Use and Privacy Statement


Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.

Please access the linked document by clicking here. Before submitting your application you will be asked to confirm your agreement with the
terms.