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Medical Device Software Engineer Jobs in Massachusetts

The Software Engineer Manager will also help bring biotechnology software development capabilities ... Manage software development activities throughout the complete medical device product lifecycle ...

New

The Software Engineer Manager will also help bring biotechnology software development capabilities ... Manage software development activities throughout the complete medical device product lifecycle ...

The Software Engineer Manager will also help bring biotechnology software development capabilities ... Manage software development activities throughout the complete medical device product lifecycle ...

New

Software Engineer Manager

Norwood, MA · On-site

$160 - $185/hr

The Software Engineer Manager will also help bring biotechnology software development capabilities ... Manage software development activities throughout the complete medical device product lifecycle ...

New

Software Architect - Medical Device Software Architect Salary Range: $200,000 - $220,000 + full ... Lead and align technical team leads and engineers with the product architecture vision. * Execution ...

Staff Quality Engineer Product Quality

Raynham, MA · On-site

$74K - $96K/yr

Support the design, development and testing of Medical Device Software, including Software as a ... Train and mentor new engineers and lower-level quality engineers. * Provide expertise in applicable ...

Staff Quality Engineer Product Quality

Boston, MA · On-site

$78K - $101K/yr

Support the design, development and testing of Medical Device Software, including Software as a ... Train and mentor new engineers and lower-level quality engineers. * Provide expertise in applicable ...

Experience in developing regulated medical device software (SaMD) under standards like IEC 62304 ... Engineering Practices, Software Quality Assurance (SQA), Systems Development Lifecycle (SDLC ...

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Showing results 1-20

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 4, 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.

How do you become a medical device software engineer?

To become a medical device software engineer, individuals typically need a bachelor's degree in software engineering, computer science, or a related field. Experience with embedded systems, programming languages like C or C++, and knowledge of medical device regulations such as FDA standards are important. Certifications in quality management or regulatory compliance can also enhance job prospects.

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 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 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 July 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 81% In-person, and 19% Remote job distribution, with an average salary of $161,114 per year, or $77.5 per hour.

Software Engineer Manager

Nova Biomedical

Norwood, MA

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New


Job description

Nova Biomedical: One Global Brand. One Vision. Together under one name.

Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets.

Job Summary:

Nova Biomedical is seeking a Software Engineer Manager to lead a local software development team supporting new product development for Nova’s osmometer platforms. This role will provide on-site leadership in Norwood for the completion of the OsmoPRO Next project and the development of the OsmoPrime and OsmoTECH XT Multi instruments. The Software Engineer Manager will also help bring biotechnology software development capabilities in-house and support the execution of Nova’s software strategy across additional product platforms.

The ideal candidate is a strong software developer and early-career manager with experience leading medical device software through the complete product lifecycle, from development and commercial release through ongoing field support. This position is expected to manage approximately four employees and may oversee both Software Engineering and Software Quality Assurance functions.

Responsibilities:

  • Lead and develop a local team of software engineers supporting osmometer new product development.
  • Provide technical and managerial leadership for the completion of the OsmoPRO Next project and the development of the OsmoPrime and OsmoTECH XT Multi instruments.
  • Manage software development activities throughout the complete medical device product lifecycle, including design, development, verification, validation, commercial release, and post-market support.
  • Ensure software development activities comply with ISO 13485 requirements and applicable medical device quality system procedures.
  • Guide the design, development, testing, integration, and maintenance of embedded and application software.
  • Provide technical direction across embedded Linux, C#/.NET, SQL, C++, and Qt-based software environments.
  • Partner with Systems Engineering, Electrical Engineering, Software Quality Assurance, Quality, Regulatory, Manufacturing, and project leadership to deliver safe, reliable, and compliant products.
  • Establish clear project priorities, resource plans, development schedules, and team objectives.
  • Monitor project execution, identify technical and scheduling risks, and drive timely resolution of issues.
  • Lead software design reviews, code reviews, troubleshooting activities, and root-cause investigations.
  • Ensure software requirements, architecture, design documentation, test records, and traceability are complete and maintained throughout the product lifecycle.
  • Support the continued development of an in-house biotechnology software platform and the integration of software capabilities associated with planned business growth and acquisition activity.
  • Recruit, coach, mentor, and evaluate software engineering team members while promoting accountability, collaboration, and technical excellence.
  • Support the management and coordination of Software Engineering and Software Quality Assurance resources.
  • Promote consistent development practices, continuous improvement, and effective knowledge sharing across the software organization.

Experience Requirements:

  • Bachelor’s degree in Software Engineering, Computer Science, Computer Engineering, Electrical Engineering, or a related technical field.
  • Experience developing software for regulated medical devices in an ISO 13485 environment.
  • Demonstrated experience supporting software through the complete medical device product lifecycle, including commercial release and field support.
  • Software development experience with embedded Linux, C#/.NET, SQL, C++, and Qt.
  • Strong understanding of software architecture, design, implementation, integration, testing, and maintenance.
  • Experience leading or managing software engineers required.
  • Experience managing or collaborating closely with Software Quality Assurance preferred.
  • Ability to balance hands-on technical leadership with team management, project planning, and employee development.
  • Knowledge of medical device software development processes, design controls, risk management, requirements traceability, verification, and validation.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent written and verbal communication skills with the ability to collaborate across technical and nontechnical teams.
  • Ability to manage multiple priorities and drive execution within a regulated product development environment.

Physical Requirements and Working Conditions:

  • Ability to work at a computer for extended periods.
  • Ability to lift and carry up to [25–50] pounds as required
  • Ability to communicate effectively via phone, video, and written communication.
  • Ability to occasionally move about the office to access meetings or resources.

Why Work for Nova Biomedical

  • Flexible Medical, Dental, & Vision Coverage
  • Competitive 401k company match
  • Bonus Program, Generous PTO and paid holidays
  • Generous Tuition reimbursement
  • Hybrid and flexible work arrangements
  • Professional development, engagement and events
  • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices
  • Company subsidized cafeteria in our Waltham, MA office

Work Location: Onsite in Norwood, MA office - 4 days/week on-site, 1 day/week remote after initial onboarding period

Targeted Salary Range: $160k-$185k

Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education.
About the Company

At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care.

Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.

With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.

Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health.

Explore what’s next with us at novabiomedical.com

EEO Statement:

Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

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