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Medical Device Software Engineer Jobs in Massachusetts

Job Title Software Design Quality Engineer The Software Design Quality Engineer is responsible for ... Track and risk assess software Anomalies for pre- and post-market medical device software.

Job TitleSoftware Design Quality Engineer The Software Design Quality Engineer is responsible for ... Track and risk assess software Anomalies for pre- and post-market medical device software.

Job TitleSoftware Design Quality Engineer The Software Design Quality Engineer is responsible for ... Track and risk assess software Anomalies for pre- and post-market medical device software.

Senior Software Engineer

Andover, MA · On-site

$129 - $184/hr

... dollar medical device industry.We are currently seeking a talented and driven Senior Software ... The Senior Software Development Engineer will have the opportunity to contribute to the full life ...

Senior Software Engineer

Andover, MA · On-site

$129K - $183K/yr

The Senior Software Development Engineer will have the opportunity to contribute to the full life ... Medical device software development experience with compliance to IEC-62304 and FDA guidelines.

Senior Software Engineer

Andover, MA · On-site

$129K - $183K/yr

... dollar medical device industry. We are currently seeking a talented and driven Senior Software ... The Senior Software Development Engineer will have the opportunity to contribute to the full life ...

Sr. Software DevOps Engineer

Newton, MA · On-site

$142K - $183K/yr

They should also be well-versed in designing, implementing, and managing DevOps practices within the healthcare, medical device, or robotics software industry. This includes deep familiarity with AWS ...

Sr. Software DevOps Engineer

Newton, MA · On-site

$142K - $183K/yr

They should also be well-versed in designing, implementing, and managing DevOps practices within the healthcare, medical device, or robotics software industry. This includes deep familiarity with AWS ...

Senior Software Engineer

Danvers, MA · On-site

$178 - $188/hr

... CT and other medical device products. * Work closely with a team of electrical, mechanical, and software engineers, both on-site and remotely. * Perform all phases of software development ...

Showing results 41-60

Medical Device Software Engineer information

See Massachusetts salary details

$69.3K

$161.1K

$224.4K

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

As of Aug 22, 2026, the average yearly pay for medical device software engineer in Massachusetts is $161,114.00, according to ZipRecruiter salary data. Most workers in this role earn between $131,100.00 and $188,900.00 per year, depending on experience, location, and employer.

What is a medical device software engineer?

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 are the 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 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 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 are the most commonly searched types of Medical Device Software Engineer jobs in Massachusetts?

The most popular types of Medical Device Software Engineer jobs in Massachusetts are:

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

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

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

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

What cities in Massachusetts are hiring for Medical Device Software Engineer jobs?

Cities in Massachusetts with the most Medical Device Software Engineer job openings:

Infographic showing various Medical Device Software Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $161,114 per year, or $77.5 per hour.

Software Design Quality Engineer

Philips

Bedford, MA • On-site

$102K - $163K/yr

Full-time

Retirement, PTO

Re-posted 25 days ago


Philips rating

8.3

Company rating: 8.3 out of 10

Based on 83 frontline employees who took The Breakroom Quiz

36th of 159 rated electronics manufacturers


Job description

Job Title
Software Design Quality Engineer
Job Description
The Software Design Quality Engineer is responsible for developing, maintaining, and managing comprehensive software quality documentation, ensuring their accuracy and regulatory compliance throughout the software lifecycle.
Your role:
  • Leads the assessment of software designs by reviewing test and performance data to uphold quality, safety, and regulatory standards, and address any engineering deficiencies.
  • Lead in the effective application, compliance, and continuous improvement of policies, procedures, and practices related to software development and validation including- Software design/verification, Risk management, Systems validation, Traceability and Cyber security risk management.
  • Track and risk assess software Anomalies for pre- and post-market medical device software.
  • Conducts detailed root cause analyses for software quality issues and validating key design inputs like usability, reliability, and performance.
  • Assess products and systems to identify defects, abnormalities and design flaws by authoring and executing software test protocols and generating test reports.
  • Implements software quality plans and risk management activities, utilizes post-market analytics to monitor software performance, and initiates corrective actions as needed.
  • Ensure compliance across the product software lifecycle by overseeing regulatory planning and execution for new products and changes as well as managing filings and approvals by overseeing preparation and submission of documentation for global registrations to enable timely market access.
  • Drive regulatory excellence and continuous improvement by developing plans, assessing risks, implementing actions, and optimizing regulatory processes for efficiency while maintaining high compliance standards.

You're the right fit if:
  • You have a minimum of 5+ years' experience in FDA regulated, IEC 62304 medical device software environments, with a focus on Software Design Assurance/Control, detailed knowledge of Risk Management (ISO 14971), SDLC and strong Understanding of all aspects of the QMS related to Software Design Controls.
  • You have proven experience in Root Cause Analysis, Software V&V, identifying/ supporting processes and design quality tools for use in tracking/preventing software defects, design traceability, Design for Quality (DfQ), Agile, and SAFe.
  • Strong experience with complex medical systems containing software, hardware and disposables.
  • You're able to share knowledge, insights regarding software quality standards, and regulatory requirements.
  • You have excellent written and verbal communication skills, with the ability to communicate and present to all levels of management.
  • Ability to interpret software design and code (C/C++/C# or any other object-oriented language) to verify implementation of requirements.
  • You have a minimum of a Bachelor's Degree (Required), in Quality, Computer Science/Engineering or similar disciplines. ISTQB certification desired.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.

How we work together:
We believe that we are better together than a part. For our Office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time (5 days per week) presence in the company's facilities. Field roles are most effectively done outside of the company's main facilities, generally at the customers' or suppliers' locations. This is an ON-SITE role.
About Philips:
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality. healthcare that we all deserve. Do the work of your life to help improve the lives of others.
  • Learn more about our business.
  • Discover our rich and exciting history.
  • Learn more about our purpose.
  • Learn more about our culture.

Philips Transparency Details:
  • The pay range for this position in Bedford, MA is $102,480 to $163,968.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.
In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here.
Additional Information:
  • US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
  • Company relocation benefits WILL NOT be provided for this position. For this position, you must reside in or within commuting distance to Bedford, MA.
  • May require travel up to 10%.

#LI-PH1
This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.
Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.

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