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Medical Device Design Jobs in Wisconsin (NOW HIRING)

Viant

Molding Process Engineer

Elkhorn, WI · On-site

Viantis a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. With nearly 6,000 ...

Verily Life Sciences LLC

WI · On-site

$150 - $200/hr

... design and development, CAPA, risk management processes per ISO 14971 and medical device software lifecycle processes per IEC 62304.* Experience supporting or managing quality across SaMD and/or AI ...

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How much do medical device design jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for medical device design in Wisconsin is $50.30, according to ZipRecruiter salary data. Most workers in this role earn between $35.43 and $60.19 per hour, depending on experience, location, and employer.

What is a medical device design?

A Medical Device Design job involves creating, developing, and improving medical devices to ensure they are safe, effective, and user-friendly. Professionals in this field work with engineers, regulatory specialists, and healthcare professionals to meet industry standards and patient needs. They use computer-aided design (CAD) software, prototyping, and testing methodologies to refine devices before production. The role requires knowledge of biomechanics, materials science, and regulatory guidelines such as FDA and ISO standards.

What are some typical challenges faced in a medical device design role?

Medical Device Design professionals often encounter challenges such as balancing innovative design with stringent regulatory requirements and ensuring devices are both effective and safe for patient use. Navigating complex approval processes, collaborating with clinicians for feedback, and keeping up with rapidly evolving technologies can also be demanding. However, these challenges make the role dynamic and rewarding, as designers play a direct role in improving patient outcomes. Team-based problem solving and ongoing learning are key parts of the job, and successfully overcoming challenges can lead to career growth and leadership opportunities within the medical device industry.

What are the key skills and qualifications needed to thrive in medical device design, and why are they important?

Success in Medical Device Design requires a solid understanding of biomedical engineering, materials science, and human anatomy, often supported by a relevant engineering degree and experience in product development. Familiarity with CAD software, rapid prototyping tools, and regulatory standards such as FDA or ISO 13485 certification is common in the field. Strong problem-solving abilities, teamwork, and effective communication help professionals excel in multidisciplinary design teams. These competencies are crucial for creating safe, innovative medical devices that meet strict quality and regulatory requirements.

What are the most commonly searched types of Medical Device Design jobs in Wisconsin?

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

What are popular job titles related to Medical Device Design jobs in Wisconsin?

For Medical Device Design jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Medical Device Design jobs in Wisconsin look for?

The top searched job categories for Medical Device Design jobs in Wisconsin are:

Medical Device Design jobs near you
Infographic showing various Medical Device Design job openings in Wisconsin as of September 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 1% Temporary, and 5% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $104,631 per year, or $50.3 per hour.

Leo Cancer Care: Senior Software Engineer - Interoperability

Middleton, WI • On-site

Centaur Health Holdings
See more jobs at Centaur Health Holdingsexternal

$125K - $165K/yr

Other

Re-posted 18 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 have demonstrated experience 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 and maintain the 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 projects in accordance with IEC 62304 and the company design 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 software component development 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 Elekta Mosaiq, and PACS servers. 
  • Proficiency with DICOM networking protocols: C-STORE, C-FIND, C-MOVE, C-GET, DICOM TLS, Storage Commitment, and Worklist services. 
  • Experience developing or maintaining a DICOM Conformance Statement. 
  • Familiarity with HL7 v2 and/or FHIR messaging as used in oncology workflows is advantageous. 
  • 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/or gRPC API 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. 
  • Proficiency with 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, with demonstrated seniority 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.