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Medical Device Software Jobs (NOW HIRING)

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 ...

Background in laboratory equipment, clinical diagnostics, or medical device development. Familiarity with the regulatory environment and standards for medical device software (e.g. IEC 62304, ISO ...

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 ...

Medical Device Assembler

Richardson, TX

$16.25 - $20/hr

We are seeking a Medical Device Assembler I to join our production team. In role, you will work in ... software is a plus Strong attention to detail and manual dexterity Ability to sit or stand for ...

Medical Device Assembler

Garland, TX

$15.75 - $19.50/hr

We are seeking a Medical Device Assembler I to join our production team. In role, you will work in ... software is a plus Strong attention to detail and manual dexterity Ability to sit or stand for ...

Medical Device Assembler

Dallas, TX

$17.50 - $21.50/hr

We are seeking a Medical Device Assembler I to join our production team. In role, you will work in ... software is a plus Strong attention to detail and manual dexterity Ability to sit or stand for ...

Medical Device Assembler

Allen, TX

$16.75 - $20.50/hr

We are seeking a Medical Device Assembler I to join our production team. In role, you will work in ... software is a plus Strong attention to detail and manual dexterity Ability to sit or stand for ...

Medical Device Assembler

Plano, TX

$16.75 - $20.50/hr

We are seeking a Medical Device Assembler I to join our production team. In role, you will work in ... software is a plus Strong attention to detail and manual dexterity Ability to sit or stand for ...

Medical Device Assembler

The Colony, TX

$16.75 - $20.50/hr

We are seeking a Medical Device Assembler I to join our production team. In role, you will work in ... software is a plus Strong attention to detail and manual dexterity Ability to sit or stand for ...

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Medical Device Software information

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$21

$49

$96

How much do medical device software jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for medical device software in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

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

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.

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.
More about Medical Device Software jobs
What cities are hiring for Medical Device Software jobs? Cities with the most Medical Device Software job openings:
What states have the most Medical Device Software jobs? States with the most job openings for Medical Device Software jobs include:
Infographic showing various Medical Device Software job openings in the United States as of June 2026, with employment types broken down into 5% As Needed, 54% Full Time, and 41% Part Time. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.
Principal Software Quality Assurance Engineer (Remote - United States)

Principal Software Quality Assurance Engineer (Remote - United States)

Healthcare

Eagan, MN

$137K - $184K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 6 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.

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