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Manager Medical Device Software Engineer Jobs in Wisconsin

Accuray

Software Engineer

Madison, WI · On-site

Experience with Medical Device development or other regulated environments. * Experience with ... configuration management such as Perforce/Git; CI/CD build, deployment, and test tooling)

Accuray Incorporated

Software Engineer

Madison, WI · On-site

Experience with Medical Device development or other regulated environments. * Experience with ... configuration management such as Perforce/Git; CI/CD build, deployment, and test tooling)

ACCURAY

Software Engineer

Madison, WI · On-site

Experience with Medical Device development or other regulated environments. * Experience with ... configuration management such as Perforce/Git; CI/CD build, deployment, and test tooling)

Kellton Tech

Medical Device Quality Inspector

Madison, WI · On-site

$30/hr

Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $30/hr (W2) Job Summary ... Reports to the Quality Control Manager. * Interfaces primarily with manufacturing, engineering, and ...

GE HealthCare

Senior Software Engineer

Waukesha, WI · On-site

$122K - $161K/yr

GE HealthCare is a leading global medical technology and digital solutions innovator. As a Senior ... management tools such as Git. Preferred : • Master's degree in Computer Science, Computer ...

GE Healthcare

Senior Software Engineer

Waukesha, WI · On-site

$122K - $161K/yr

GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose ... Proficiency in configuration management tools such as Git. Desired Characteristics * Master ...

GE HealthCare

Senior Software Engineer

Waukesha, WI · On-site

$122K - $161K/yr

GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose ... Proficiency in configuration management tools such as Git. Desired Characteristics * Master ...

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Manager Medical Device Software Engineer information

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

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

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

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

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

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

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

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

Manager Medical Device Software Engineer jobs near you

Software Engineer

Accuray

Madison, WI • On-site

Full-time

Re-posted 9 days ago

Job description

Give hope. Give health. Make your mark in the fight against cancer.

At Accuray, we make a direct and powerful impact on the lives of cancer patients every day - helping them live longer, better lives. But our commitment to innovation offers a truly unique opportunity: the chance to change the fight against cancer - helping to develop, introduce and support new treatment delivery systems and software that will give new hope and new health to cancer patients and cancer survivors around the world.

Accuray develops, manufactures and sells radiotherapy systems for alternative cancer treatments. Our radiation therapy for cancer makestreatment shorter, safer, personalized and more effective, ultimately enabling patients to live longer, better lives.

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES

Software Development (Build, Extend, Maintain)

  • Develop and maintain software that supports thelifecycleof a complex radiation therapy medical device.

  • Write high-quality, reliable code that fulfills product and subsystem requirements in a complex clinical domain.

  • Implement automated tests (unit/integration as appropriate) to validate functionality and reduce regressions.

  • Contribute to sustaining engineering by troubleshooting, participating in root-cause analysis, and resolving issues found in new or existing functionality.

Software Design & Architecture (Make the System Better)

  • Directoyimpactthe development and architecture of software that creates, stores, optimizesand deliverspatient treatments.

  • Drive critical design and implementation decisions and participate in design discussions for complex systems.

  • Present concise designs through written and oral reviews; contribute to clear documentation of designs, decisions, and outcomes.

  • Contribute to subsystem requirements and verification approaches for new features.

Performance & Computational Solutions (Accuracy + Responsiveness)

  • Participate in decisions affecting high-performance computation solutions to provide responsive and accurate results that meet clinical expectations.

  • Collaborate on technology choices (e.g., languages/libraries, compute approaches) to support performance, maintainability, and testability.

Quality, Compliance, and Ways of Working

  • Work closely with team members to implement quality applications that meet or exceed rigorous testing expectations.

  • Operate effectively in a regulated industry with strict process requirements; document work and follow the defined development processes.

  • Support continuous improvement efforts (e.g., coding standards, code reviews, test coverage, build/test automation) to increase engineering efficiency without sacrificing quality.

Collaboration & Technical Contribution

  • Collaborate across disciplines (software, systems, test, product, clinical/field stakeholders as needed) to deliver integrated solutions.

  • Cross-pollinate the team with theory and practice of software development, object-oriented design, and computer languages.

  • Proactively share information and communicate technical status, risks, and decisions to the rightaudiencesat the right level of detail.

Travel

  • Some travel (<10%) may be required.

QUALIFICATIONS

Required

  • BS in Computer Science, Computer Engineering, or an equivalent combination of education and experience.

  • Proficiency in C++ (object-oriented development), C# orrelatedlanguage.

  • Experience with automated unit testing frameworks and building/maintaining testable code.

  • Experience with object-oriented analysis & design, including correct use of design patterns and awareness of anti-patterns. Experience with client/server architecture. Strong written and verbal communication skills; able to present and defend designs in reviews.

  • Must be able to work effectively in a team environment

Preferred

  • Strong mathematics and/or physics background.

  • Experience with Medical Device development or other regulated environments.

  • Experience with modern software practices and toolchains (e.g., configuration management such as Perforce/Git; CI/CD build, deployment, and test tooling).

  • Experience with Python or related languages.

  • Experiencewith client / server architecture.

  • Experience developing software in multi-threaded / multi-core environments.

WORKING CONDITIONS

Office:

  • Indoor Environment: The position takes place indoors, providing a comfortable and climate-controlled workspace.

  • Sedentary Work: This role involves extended periods of sitting and working at a desk, requiring good ergonomicpractices.

  • Computer Usage: Proficiency with computers, including software applications and communication tools, is essential for tasks and collaboration.

  • Minimal Physical Strain: While physical demands are generally low, occasional light lifting and moving of objects might be required.

  • Structured Schedule: This position usually follows regular business hours, promoting a consistent and predictable work routine.

To qualify for this position, candidates must be able to furnish proof that they are authorized to work in the country they are applying on a permanent basis without sponsorship.

EEO Statement

At Accuray, our commitment to patient-first outcomes drives an inclusive and collaborative work environment where the best ideas rise to the top - and everyone works to push them further. We value diversity in both the professional and personal backgrounds of our employees, as this variety adds rich energy to every team, every project and every work day. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or national origin - including individuals with disabilities and veterans.

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