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Engineering Medical Device Jobs in Wisconsin (NOW HIRING)

Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all ...

Senior Manufacturing Engineer

Hudson, WI · On-site

$78K - $124K/yr

Overview Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion ...

Senior Manufacturing Engineer

Hudson, WI · On-site

$78K - $124K/yr

Overview Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion ...

Bachelor's degree in Electrical Engineering or related field (advanced degree preferred); equivalent medical device experience may substitute * 5+ years of experience in complex medical device design ...

... Engineering, or equivalent experience. 2+ years Minimum in Medical Device or Pharmaceutical Industry or similar experience. 2+ years Minimum in a Quality Role. 2+ years Minimum in a Validation ...

... Engineering, or equivalent experience. 2+ years Minimum in Medical Device or Pharmaceutical Industry or similar experience. 2+ years Minimum in a Quality Role. 2+ years Minimum in a Validation ...

Quality Engineer II

Kenosha, WI

$70K - $90K/yr

Bachelor's degree in Quality Engineering, Mechanical Engineering, Biomedical Engineering, or a related field preferred or equivalent experience * five to seven years of experience in medical device ...

Prior experience in medical device or regulated industries . Education Requirement: Bachelor's degree in Mechanical Engineering or related field; 5-10 years of experience preferred Industry ...

Showing results 41-60

Engineering Medical Device information

See Wisconsin salary details

$21

$50

$97

How much do engineering medical device jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for engineering medical device 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 an engineering medical device professional?

Engineering medical device professionals are specialists who design, develop, test, and improve medical devices used in healthcare. They combine principles of engineering, biology, and medicine to create equipment such as pacemakers, imaging machines, and prosthetics that help diagnose, treat, or manage medical conditions. Their work ensures devices are safe, effective, and comply with regulatory standards. These professionals often work closely with doctors, patients, and regulatory agencies throughout the product development process.

What are the key skills and qualifications needed to thrive as a medical device engineer?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant degree and knowledge of FDA regulations. Familiarity with CAD software, prototyping tools, and quality management systems is typically required, along with certifications like Six Sigma or ISO 13485. Strong problem-solving abilities, teamwork, and effective communication are standout soft skills in this role. These competencies are crucial for designing safe, innovative devices that meet regulatory standards and improve patient outcomes.

What are some typical challenges faced by engineers working in the medical device industry?

Engineers in the medical device industry often face challenges related to strict regulatory compliance, such as meeting FDA or ISO standards. Additionally, they must ensure that devices are safe, effective, and user-friendly, requiring frequent collaboration with cross-functional teams like clinical, quality assurance, and manufacturing. Balancing innovation with patient safety while managing tight project timelines is also a common aspect of the role. Overcoming these challenges can be rewarding, as it directly contributes to improving patient outcomes.

What is the difference between Engineering Medical Device vs Biomedical Engineer?

AspectEngineering Medical DeviceBiomedical Engineer
Required CredentialsEngineering degree, possibly certifications in medical device designEngineering or biomedical degree, certifications in healthcare technology
Work EnvironmentDesign labs, manufacturing facilities, regulatory agenciesHospitals, research labs, healthcare companies
Employer & Industry UsageMedical device companies, biotech firms, regulatory bodiesHospitals, medical research institutions, healthcare technology firms

Engineering Medical Device professionals focus on designing, developing, and testing medical devices, often working in manufacturing or regulatory settings. Biomedical Engineers have a broader scope, integrating engineering principles with biological sciences to improve healthcare solutions, including medical devices. While both roles require engineering backgrounds, Engineering Medical Device specialists typically concentrate on product development, whereas Biomedical Engineers may work on research, clinical applications, or device integration.

What does an engineering medical device do?

An engineering medical device professional designs, develops, and tests medical equipment such as diagnostic tools, surgical instruments, and monitoring systems. They apply engineering principles, often using CAD software and regulatory standards, to ensure devices are safe, effective, and compliant with healthcare regulations.

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

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

Infographic showing various Engineering Medical Device job openings in Wisconsin as of August 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $104,631 per year, or $50.3 per hour.

Leo Cancer Care: Senior Software Engineer - Interoperability

Leo Cancer Care

Middleton, WI • Hybrid

$125K - $165K/yr

Full-time

Posted 25 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.