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Medical Device Software Engineer Jobs in Wisconsin

As a Software Engineer, you will help establish the low-level software foundation that enables ... medical devices, including operating system configuration, board support packages, device drivers ...

Embedded Software Engineer

Wauwatosa, WI

$127K - $168K/yr

... medical device software Qualifications Requirements: Bachelor's Degree in Electrical Engineering, Computer Engineering, Computer Science or related computer degree 5 years' experience in embedded ...

Bachelor's degree in Computer Science, Software Engineering, Computer Engineering, or related ... Must have experience in a medical device field (or similar: pharma). Strong understanding of ...

Bachelor's degree in Computer Science, Software Engineering, Computer Engineering, or related ... Must have experience in a medical device field (or similar: pharma). Strong understanding of ...

Job Title: Medical Device Assembler Location: Madison, WI (Onsite) Pay Rate: $23-24/hr on W2 ... Engineering group as required. Working Conditions: Clean, temperature controlled environment.

Hi - My direct client is looking for a Software Engineer. If you're interested, please email me ... Experience in medical device or FDA‑regulated industries. * Knowledge of data integrity rules ...

Job Title: Medical Device Quality Engineer Location: Madison, WI Pay Rate : $40--45/hr on W2 ... Experience with statistical analysis software (e.g., Minitab preferred) Organizational Relationship ...

Medical Device Technician

Madison, WI · On-site

$38K - $48K/yr

Medical Device Technician Location: Madison, WI (Onsite) Scope of Work: Assemble and test medical ... Bachelor's degree in engineering or related scientific field. Associate's degree with 2+ years ...

The Software engineer collaborates in a complex environment integrating software with other ... software and hardware subsystems for an advanced medical device. Our work has a daily impact on ...

The Software engineer collaborates in a complex environment integrating software with other ... software and hardware subsystems for an advanced medical device. Our work has a daily impact on ...

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Showing results 1-20

Medical Device Software Engineer information

See Wisconsin salary details

$64.1K

$148.9K

$207.4K

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

As of Aug 5, 2026, the average yearly pay for medical device software engineer in Wisconsin is $148,903.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,100.00 and $174,600.00 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 Wisconsin? The most popular types of Medical Device Software Engineer jobs in Wisconsin are:
What are popular job titles related to Medical Device Software Engineer jobs in Wisconsin? For Medical Device Software Engineer jobs in Wisconsin, the most frequently searched job titles are:
Infographic showing various Medical Device Software Engineer job openings in Wisconsin as of July 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 82% In-person, and 18% Remote job distribution, with an average salary of $148,903 per year, or $71.6 per hour.

Leo Cancer Care: Senior Software Engineer - Interoperability

Leo Cancer Care

Middleton, WI • Hybrid

$125K - $165K/yr

Full-time

Posted 15 days ago


Job description

Position Title: Senior Software Engineer - Interoperability

Reports to: Senior Manager Global Software Engineering

FT/PT : Full-time

Location: US Office, Hybrid- Office 3 days a week

Position Summary: Join our dynamic engineering team to help develop our revolutionary radiotherapy products for upright therapy. This role sits at the intersection of medical device software engineering and clinical systems integration, with a primary focus on DICOM-RT interoperability between our treatment system and the broader clinical ecosystem - including Oncology Information Systems (OIS), PACS servers, and other networked medical devices.

The ideal candidate brings deep hands-on experience with DICOM-RT standards, network-level system integration, and medical device software development under IEC 62304. You will play a key technical leadership role in defining and implementing the interoperability architecture that connects our treatment delivery system to the clinical workflow, working closely with partners, clinical customers, and internal cross-functional teams.

The position requires flexibility in daily tasks with attention to detail and a self-motivated work ethic. The successful candidate will havedemonstratedexperience working in cross-functional and cross-disciplinary teams and providing technical leadership in the development of novel products.

Key responsibilities:

  • Lead the design, specification, and implementation of DICOM-RT interoperability features, including RT Plan, RT Dose, RT Structure Set, RT Image, and RT Ion Plan objects.
  • Architect and develop network API interfaces enabling communication between the treatment delivery system, OIS (e.g.ARIA,Mosaiq), and PACS servers.
  • Define andmaintainthe system's DICOM Conformance Statement and related integration documentation.
  • Drive end-to-end integration testing with clinical systems, including HL7/FHIR messaging where applicable.
  • Perform as a technical lead on significant software development projects spanning interoperability and clinical connectivity.
  • Write specifications, requirements, design documents, and test protocols for software projectsin accordance withIEC 62304 and thecompanydesign control process.
  • Develop safety-critical software for imaging and treatment delivery systems.
  • Work with external partners and clinical customers to develop,validate, and support system interfaces and integrations.
  • Contribute to the design and development of service and validation tools for DICOM interoperability.
  • Provide engineering support to partners, customers, and field service teams.
  • Support regulatory submissions (e.g.510(k)) as they relate to interoperability and software.
  • Contribute to system architecture and software development process improvements.
  • Mentor less experienced engineers in interoperability standards and medical device software practices.
  • Manage contractors relating to softwarecomponentdevelopment where applicable.

Relevant Knowledge and Skill requirements:

DICOM-RT and Clinical Interoperability

  • Deep working knowledge of DICOM-RT standards: RT Plan, RT Dose, RT Structure Set, RT Image, RT Ion Plan, and related SOP classes.
  • Practical experience integrating radiotherapy treatment systems with Oncology Information Systems (OIS) such as Varian ARIA or ElektaMosaiq, and PACS servers.
  • Proficiencywith DICOM networking protocols: C-STORE, C-FIND, C-MOVE, C-GET, DICOM TLS, Storage Commitment, and Worklist services.
  • Experience developing ormaintaininga DICOM Conformance Statement.
  • Familiarity with HL7 v2 and/or FHIR messaging as used in oncology workflows isadvantageous.
  • Understanding of IHE Radiation Oncology profiles (e.g.RO-PIR, IHE-RO) is a plus.

Medical Device Software Engineering

  • Proven experience developing medical device software in compliance with IEC 62304, including software lifecycle planning, classification, architecture, unit testing, and maintenance.
  • Familiarity with associated standards and guidance: ISO 14971 (risk management), IEC 62443 (cybersecurity), and applicable FDA/CE regulatory requirements for software.
  • Experience supporting regulatory submissions (510(k), CE Technical File) for software-intensive medical devices.
  • Experience with design and specification of software systems using UML.

Networking and Software Engineering

  • Solid understanding of TCP/IP networking: routing, firewalls, VLANs, TLS/SSL, and network security as it applies to connected medical devices.
  • Experience with REST and/orgRPCAPI design and integration in a clinical or embedded systems context.
  • Strong programming skills in Python and at least one of C++, C#, or Java.
  • Experience with Linux, shell scripting, and systems-level debugging.
  • Proficiencywith version control (Git), CI/CD pipelines, and software testing frameworks.

Experience

  • Minimum 5 years of domain-specific experience in medical device software engineering within radiotherapy, radiation oncology, or a closely related imaging/treatment modality.
  • 10+ years of total software engineering experience, withdemonstratedseniority in at least one prior role, is strongly preferred.
  • Experience working in cross-functional teams including clinical physics, systems engineering, quality, and regulatory affairs.
  • Ability to mentor and provide technical leadership to less experienced engineers.

About Leo Cancer Care

Leo Cancer Care is helping make changes in Radiation Therapy by shifting to upright patient positioning, imaging and treatment. We do what we do to find a better way, a better way to treat cancer and create a paradigm shift in radiation therapy to benefit all. We will do this by improving the accessibility and medicine in cancer care globally, making cancer treatment a more human experience for all.

Working in radiotherapy not only will you be driving change for the greater good, but you'll be working on products that span a large field of different disciplines.

Ways of Working

Leo Cancer Care is dedicated to fostering a diverse and inclusive workplace environment. We embrace and celebrate the unique backgrounds, experiences, and perspectives of all individuals. We believe that diversity enriches our organization and strengthens our ability to innovate and excel. Discrimination or harassment of any kind will not be tolerated. We encourage all qualified candidates to apply and join us in our mission to create a respectful and equitable workplace for all.


Leo Cancer Care is an equal opportunity employer.