ZipRecruiter

Log In

1

Medical Device Cybersecurity Jobs in Wisconsin (NOW HIRING)

Standard Imaging Inc

IT Manager

Middleton, WI · Remote

$97K - $119K/yr

... small-mid-size medical device organization. This role is ideal for a technically strong ... Support cybersecurity initiatives including endpoint and identity protection * Administer tools ...

GE HealthCare

Senior Systems Engineer

Waukesha, WI · On-site

$104K - $143K/yr

... products throughout the medical device development lifecycle, from concept through ... cybersecurity, and safety requirements. * Lead cross-functional development teams across ...

Standard Imaging, Inc

IT Manager

Middleton, WI · On-site

$97K - $119K/yr

... small-mid-size medical device organization. This role is ideal for a technically strong ... Support cybersecurity initiatives including endpoint and identity protection * Administer tools ...

Gehc

Lead Systems Designer

Waukesha, WI

$110K - $144K/yr

Own all systems engineering tasks for your product throughout the medical device development phases ... Knowledge of software design principles, cybersecurity principles, cloud development, microservice ...

Gehc

Senior Systems Engineer

Waukesha, WI · Hybrid

$104K - $143K/yr

... products throughout the medical device development lifecycle, from concept through ... cybersecurity, and safety requirements. * Lead cross-functional development teams across ...

GE HealthCare

Lead Systems Engineer

Waukesha, WI · On-site

Own all systems engineering tasks for your product throughout the medical device development phases ... Knowledge of software design principles, cybersecurity principles, cloud development, microservice ...

Ellsworth

Chief Technology Officer

Germantown, WI · Hybrid

... medical device, space/aerospace, and electric vehicle industries!Click here to see our ... Provide executive oversight of cybersecurity posture, risk management, and resilience planning

Surgery Partners

Biomedical Engineer

Altoona, WI · On-site

Support cybersecurity initiatives for connected medical devices in collaboration with Information ... medical device technology * Working knowledge of applicable healthcare regulations and ...

GE HealthCare

Senior Program Manager - Cardiology

Waukesha, WI · On-site

$116K - $116K/yr

... cybersecurity, and regulatory compliance. Roles and Responsibilities The Senior Program Manager ... regulated medical device product development processes. * Ability to develop unique concepts ...

Gehc

Senior Program Manager - Cardiology

Waukesha, WI · Hybrid

$116K - $116K/yr

... cybersecurity, and regulatory compliance. Roles and Responsibilities The Senior Program Manager ... regulated medical device product development processes. * Ability to develop unique concepts ...

Flen Health Group S.A.

WI · On-site

$137.06 - $205.60/hr

... medical device technological domain. Flen Health has a range of products for wound and skin care ... Ensure data governance, cybersecurity, system reliability, and information integrity* Lead IT and ...

Flen Health

WI · On-site

$171.33 - $217.02/hr

... medical device technological domain. Flen Health has a range of products for wound and skin care ... Ensure data governance, cybersecurity, system reliability, and information integrity* Lead IT 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 ... virtual machines, cyber security, Linux operating system, and packaging technologies.

previous pagenext page

Showing results 21-40

All JobsMedical Device Cybersecurity JobsMedical Device Cybersecurity Jobs in Wisconsin

Medical Device Cybersecurity information

What are some common challenges faced by professionals in medical device cybersecurity, and how can they be addressed?

Professionals in medical device cybersecurity often encounter challenges such as integrating security measures into legacy devices, ensuring compliance with evolving regulations, and balancing usability with robust protection. Collaborative efforts with engineering, regulatory, and clinical teams are crucial to embedding security throughout the product lifecycle. Staying current with threat intelligence and participating in cross-functional risk assessments also help anticipate and address vulnerabilities proactively.

What is medical device cybersecurity?

Medical device cybersecurity refers to the protection of medical devices and the data they process from cyber threats and unauthorized access. As medical devices become increasingly connected to hospital networks and the internet, robust cybersecurity measures are essential to ensure patient safety and protect sensitive health information. This field involves identifying vulnerabilities, implementing safeguards, and complying with regulatory requirements to reduce the risk of cyberattacks on medical technology.

What is the difference between Medical Device Cybersecurity vs Medical Device Quality Assurance?

AspectMedical Device CybersecurityMedical Device Quality Assurance
Required CredentialsCertifications in cybersecurity, such as CISSP or CISA; knowledge of medical device regulationsCertifications in quality management, like CQE or ISO 13485 auditor
Work EnvironmentIT security teams, R&D, regulatory compliance in healthcare settingsManufacturing, clinical, and regulatory environments focused on product quality
Employer & Industry UsageMedical device manufacturers, healthcare providers, cybersecurity firmsMedical device companies, regulatory agencies, quality assurance firms

Medical Device Cybersecurity focuses on protecting medical devices from cyber threats, ensuring data integrity and security. Medical Device Quality Assurance emphasizes maintaining product quality, safety, and compliance throughout development and manufacturing. While both roles support patient safety, cybersecurity specialists address digital vulnerabilities, whereas quality assurance professionals ensure the device meets regulatory standards.

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

To thrive in Medical Device Cybersecurity, you need a solid background in cybersecurity principles, risk management, and biomedical engineering, often supported by a relevant degree and certifications like CISSP or CISM. Familiarity with regulatory standards (such as FDA cybersecurity guidelines), network security tools, and vulnerability assessment systems is essential. Strong analytical thinking, attention to detail, and effective communication skills help professionals collaborate with cross-functional teams and address complex security challenges. These skills are crucial to ensure medical devices remain secure from cyber threats, protecting patient safety and maintaining regulatory compliance.
What job categories do people searching Medical Device Cybersecurity jobs in Wisconsin look for? The top searched job categories for Medical Device Cybersecurity jobs in Wisconsin are:
What cities in Wisconsin are hiring for Medical Device Cybersecurity jobs? Cities in Wisconsin with the most Medical Device Cybersecurity job openings:
Medical Device Cybersecurity jobs near you
Infographic showing various Medical Device Cybersecurity job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

LabVIEW/Test Automation Engineer

HonorVet Technologies

Madison, WI • On-site

$46.25 - $61.25/hr

Other

Posted 17 days ago

Job description

HonorVet Technologies (SDVOSB) is a certified veteran-owned staffing and workforce solutions company recognized for its industry certifications, commitment to quality talent acquisition, and excellence in delivering IT, healthcare, federal, state, and SLED (State, Local, and Education) staffing services, helping organizations build reliable, compliant, and high-performing teams across mission-critical sectors.
 
Title: LabVIEW/Test Automation Engineer
Duration: 06 Months
Location: Madison, WI, 53718
Work model: Onsite
Interview Mode: 1st Round web and next onsite
 
Job Summary:
We are seeking an experienced Computer Engineer to support the Sustaining Engineering team responsible for maintaining and improving test systems, automated equipment, and supporting software used in the manufacture of FDA‐regulated medical devices for respiratory therapy. This role focuses on test and support systems not directly embedded in the therapeutic device, but which are essential for product verification, production workflows, and device commissioning.
The ideal candidate has strong software engineering skills, hands-on experience with automated test systems, and deep familiarity with regulated environments (FDA 21 CFR Part 820.72, GMP). They will ensure test system reliability, maintain compliance, support cybersecurity controls, and drive continuous improvement across manufacturing support technologies.
 
Key Responsibilities:
Software Development & Test System Engineering
  • Develop, maintain, and optimize test and automation software using LabVIEW, NI TestStand, and Python.
  • Write efficient and scalable code in Python for backend testing, data processing, and hardware/software integration.
  • Design and implement software solutions that interface with sensors, industrial PCs, DAQ modules, and automated machinery.
  • Assist in developing test frameworks, scripts, and utilities used for software/system validation.
  • Debug complex code and system behavior across Windows 11, industrial PCs, and embedded device interfaces.
 Systems Support & Troubleshooting
  • Diagnosing and resolving issues in complex test and measurement systems, including hardware/software interactions and system-level faults.
  • Support enterprise IT systems used for device commissioning, access control, configuration management, and backup/recovery processes.
  • Perform root cause analysis (RCA) on system failures and implement corrective and preventive actions (CAPA).
 Cross-Disciplinary Engineering Support
  • Partner with Electrical and Mechanical Engineering teams to investigate complex system behaviors involving hardware–software integration.
  • Analyze ambiguous or intermittent production test issues where failures are present in subtle, non-obvious ways to users or operators.
  • Develop software tools, instrumentation scripts, and diagnostic routines to capture hidden failure modes that traditional hardware diagnostics may not detect.
  • Contributes to the creation of advanced test strategies that correlate data across mechanical, electrical, and software subsystems.
 Regulatory & Compliance Responsibilities
  • Work within FDA 21 CFR Part 820.72 and applicable GMP quality system requirements.
  • Ensure data integrity, cybersecurity protections, audit trails, and access controls are properly implemented in test systems.
  • Maintain clear, compliant documentation of code, workflows, and validation processes.
  • Participate in risk analysis and support validation/verification activities for test equipment and software tools.
 Collaboration & Technical Leadership
  • Collaborate with cross-functional teams including Manufacturing Engineering, Quality, IT Security, and R&D.
  • Translate production and engineering needs into technical requirements for software and test systems.
  • Train users and provide engineering support for manufacturing personnel and test technicians.
 Required Qualifications:
  • Bachelor’s degree in Computer Engineering, Software Engineering, Electrical Engineering, or related field.
 Strong proficiency in:
  • LabVIEW
  • Python
  • High-level languages (C++, Java) and associated development environments
  • Scripting languages for automation/test development
 Experience working with:
  • Windows 11 OS and PC hardware architectures
  • Industrial PCs and automated test hardware
  • GitHub, source control, debuggers, build systems
  • TestStand or similar automated test frameworks
  • Hands-on experience debugging complex embedded or computerized systems.
  • Understanding of the software development lifecycle (SDLC).
  • Experience with root cause analysis, fault isolation, and system troubleshooting.
 Familiarity with cybersecurity fundamentals related to:
  • Access control
  • Data protection
  • System administration
  • Networked test systems
 Preferred Qualifications:
  • Prior experience in a medical device or other FDA-regulated industry.
  • Knowledge of data integrity requirements, ALCOA/ALCOA+ principles, and digital recordkeeping compliance.
  • Experience validating software or equipment under GxP frameworks.
  • Background in test equipment calibration, test method validation, or automated manufacturing tools
 Soft Skills:
  • Strong communication and documentation abilities.
  • Detail-oriented with a disciplined approach to working within regulated processes.
  • Ability to manage multiple tasks, prioritize effectively, and collaborate across diverse teams.
  • Problem-solving mindset with a focus on system reliability and continuous improvement.
  • Domestic and international travel of up to 20% may be required to support manufacturing sites, suppliers, and field issue investigations.
HonorVet Technologies logo

About HonorVet Technologies

Sourced by ZipRecruiter

HonorVet Technologies, located in Fairfield, NJ, US, is a technology-driven company with a unique dimension - enhancing veteran engagement in the workforce. Founded with the goal of supporting and preserving professional veterans while satisfying the IT and professional needs of businesses, HonorVet Technologies brings a particular focus to diversity and veteran hiring, making it a standout player in the IT and Staffing industries. Functioning as a veteran-driven community entity, the firm offers IT staffing, bespoke development, and consulting services, with the aim of connecting talents with IT-related job opportunities.

Industry

Recruiting and staffing services

Company size

201 - 500 Employees

Headquarters location

Fairfield , NJ, US

Year founded

2015

View All HonorVet Technologies Jobs

Apply