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Manager Medical Device Software Engineer Jobs in Manchester, NH

Suntra MedTech Solutions

Software Architect

Bedford, NH · On-site

... for medical device software. * Risk Management & Cybersecurity: Integrate safety measures and ... Bachelor's degree in software engineering, Computer Science, Electrical Engineering, or a related ...

DEKA

Software Quality Assurance Engineer

Manchester, NH · On-site

Embed with engineering teams to understand existing documentation practices and automation tools ... Practical knowledge of ISO 14971 risk management methodology as applied to medical device software ...

Fresenius Kabi

Sr Engineer (Control Systems)

Andover, MA · On-site

$169K - $175K/yr

Job Summary The Sr Engineer (Control Systems) works on the design and development of the control ... medical device software applications with minimal supervision Performs configuration management ...

Globus Medical

Software Engineer

Methuen, MA · On-site

We are currently seeking a Software Engineer for our Methuen, MA office. This person will be ... Experience in Medical Device field a plus * Ability to work independently and as a key contributor ...

Globus Medical

Software Engineer

Methuen, MA · On-site

We are currently seeking a Software Engineer for our Methuen, MA office. This person will be ... Experience in Medical Device field a plus * Ability to work independently and as a key contributor ...

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All JobsMedical Device Software Engineer JobsManager Medical Device Software Engineer JobsManager Medical Device Software Engineer Jobs in Manchester, NH

Manager Medical Device Software Engineer information

See Manchester, NH salary details

$99.1K

$168.6K

$199.6K

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

As of Aug 5, 2026, the average yearly pay for manager medical device software engineer in Manchester, NH is $168,648.00, according to ZipRecruiter salary data. Most workers in this role earn between $172,300.00 and $172,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a manager medical device software engineer, and why are they important?

To thrive as a Manager Medical Device Software Engineer, you need expertise in software development, medical device regulations (such as FDA or ISO 13485), and a background in engineering or computer science, often supported by advanced degrees or certifications. Familiarity with tools like version control systems (e.g., Git), embedded systems platforms, and quality management software is essential, along with understanding regulatory documentation processes. Strong leadership, effective communication, and problem-solving abilities distinguish top performers in this role. These skills are crucial for ensuring safe, compliant, and innovative medical device software development while leading teams to deliver high-quality products.

How does a manager medical device software engineer typically collaborate with cross-functional teams during product development?

A Manager Medical Device Software Engineer frequently works alongside teams such as regulatory affairs, quality assurance, hardware engineering, clinical specialists, and marketing. They coordinate software development activities to ensure compliance with industry standards and regulatory requirements, while also aligning software features with clinical and business needs. These managers often lead design reviews, facilitate risk assessments, and ensure effective communication between software engineers and non-technical stakeholders. This collaborative environment is essential for delivering safe, effective, and user-friendly medical devices.

What does a manager medical device software engineer do?

A Manager Medical Device Software Engineer oversees teams that design, develop, and maintain software for medical devices. They ensure that the software complies with regulatory standards, works reliably, and meets the needs of healthcare professionals and patients. In addition to technical leadership, they coordinate with cross-functional teams, manage project timelines, and mentor engineers. Their role is critical in ensuring products are both safe and effective for use in medical settings.
What are popular job titles related to Manager Medical Device Software Engineer jobs in Manchester, NH? For Manager Medical Device Software Engineer jobs in Manchester, NH, the most frequently searched job titles are:
What job categories do people searching Manager Medical Device Software Engineer jobs in Manchester, NH look for? The top searched job categories for Manager Medical Device Software Engineer jobs in Manchester, NH are:
Manager Medical Device Software Engineer jobs near you

Software Architect

Suntra MedTech Solutions

Bedford, NH • On-site

Other

Re-posted 29 days ago

Job description

Description

Position Overview: Responsible for the high-level architecture and design of medical device software, ensuring alignment with system and software requirements. This "hands-on" role requires you to be in our Bedford, NH office (on a scheduled basis) to collaborate with project managers and software teams on multiple projects. The role includes reviewing detailed designs, the testing structure, and code, while also focusing on risk management and cybersecurity to ensure device safety for users and clinicians. It also offers the chance to lead technical initiatives, guide engineering teams, and make a significant impact on the development of medical devices.


Key Responsibilities:

  • Architecture & Design: Develop scalable, secure, and compliant software architecture based on system and software requirements.
  • Collaboration & Leadership: Work closely with project managers and software teams, providing architectural guidance and mentoring engineers.
  • Code Quality & Reviews: Conduct code reviews, enforce coding standards, and ensure high-quality, maintainable code.
  • Regulatory Compliance: Ensure adherence to regulatory standards (e.g., IEC 62304) for medical device software.
  • Risk Management & Cybersecurity: Integrate safety measures and conduct risk assessments to ensure device safety.
  • Continuous Improvement: Advocate for best practices, evaluate new technologies, and enhance development processes.

Requirements

Qualifications:

  • Required: Bachelor's degree in software engineering, Computer Science, Electrical Engineering, or a related field; 10+ years of industry experience; proficiency in programming languages (e.g., C, C#, C++, JavaScript); experience with embedded systems, and medical device development; familiarity with Agile/Scrum processes.
  • Beneficial: Master's degree; experience in Class B and C medical devices; Linux OS configuration; familiarity with test-driven development (TDD), CI/CD, and regulatory standards like IEC 62304.
  • Preferred: Experience using generative AI to aid in software development, developing machine learning-based products, knowledge of embedded Linux, real-time operating systems (RTOS), and cybersecurity hardening, as well as familiarity with Atlassian tools and software development best practices.

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