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Medical Device Testing Jobs in Wisconsin (NOW HIRING)

Quality Engineer II

Kenosha, WI

$70K - $90K/yr

... testing activities to ensure continuous control over materials, facilities, and products. • ... Knowledge of the medical device manufacturing industry is highly preferred. * Experience with CNC ...

Product Design Engineer, IoT

Madison, WI · On-site

$130K - $156K/yr

... testing, and validation aligned with product and regulatory requirements to meet product ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Product Design Engineer, IoT

Madison, WI

$130K - $156K/yr

... testing, and validation aligned with product and regulatory requirements to meet product ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Product Design Engineer, IoT

Madison, WI · On-site

$130K - $156K/yr

... testing, and validation aligned with product and regulatory requirements to meet product ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Product Design Engineer, IoT

Madison, WI · On-site

$130K - $156K/yr

... testing, and validation aligned with product and regulatory requirements to meet product ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Software Project Lead

Waukesha, WI · Hybrid

$55 - $65/hr

Support a software organization consisting of developers and testers working on desktop software applications used within medical device products Required Qualifications * Experience as a Scrum ...

Software Project Lead

Waukesha, WI · Hybrid

$55 - $65/hr

Support a software organization consisting of developers and testers working on desktop software applications used within medical device products Required Qualifications * Experience as a Scrum ...

Software Project Lead

Waukesha, WI · Hybrid

$55 - $65/hr

Support a software organization consisting of developers and testers working on desktop software applications used within medical device products Required Qualifications * Experience as a Scrum ...

Quality Assurance Engineer II

Sturgeon Bay, WI · On-site

$69K - $89K/yr

... medical device regulations. Your role supports new product introduction by developing and implementing inspection, testing, and validation methods to ensure reliable manufacturing processes and ...

Quality Engineer II

Kenosha, WI · On-site

$70K - $90K/yr

... testing activities to ensure continuous control over materials, facilities, and products. • ... Knowledge of the medical device manufacturing industry is highly preferred. * Experience with CNC ...

The Software Engineer participates in requirements, design, development, integration, and testing ... Experience with Medical Device development or other regulated environments. * Experience with ...

Showing results 21-40

Medical Device Testing information

See Wisconsin salary details

$21

$37

$71

How much do medical device testing jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for medical device testing in Wisconsin is $37.07, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $46.35 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Medical Device Testing position, and why are they important?

To thrive in Medical Device Testing, you need a strong background in biomedical engineering, quality assurance, and regulatory compliance, often supported by a relevant degree. Hands-on experience with testing equipment, validation protocols, and familiarity with standards such as ISO 13485 and FDA guidelines are typically required. Attention to detail, analytical thinking, and clear documentation skills are essential soft skills for excelling in this field. These abilities ensure that devices meet safety and performance standards, protecting patient health and supporting company compliance.

What are some typical daily responsibilities for someone working in Medical Device Testing?

Professionals in Medical Device Testing typically spend their days conducting tests on new or existing medical devices to ensure they meet quality, safety, and regulatory standards. This often involves following strict protocols, documenting results accurately, and troubleshooting any performance or compliance issues that arise. Team members frequently collaborate with engineers, regulatory specialists, and manufacturing staff to ensure seamless product development and problem resolution. There may also be tasks related to preparing reports for regulatory submissions or participating in audits. This role offers the opportunity to make a real impact on patient safety while working in a collaborative, fast-paced environment.

What is a Medical Device Testing job?

A Medical Device Testing job involves evaluating medical devices to ensure they meet regulatory standards, safety guidelines, and performance requirements. Professionals in this role conduct tests, analyze data, and document results to verify compliance with industry regulations such as FDA, ISO, and IEC standards. They work with engineers and regulatory teams to identify design flaws, improve product safety, and ensure reliability before market release. This job is crucial for preventing defects that could impact patient health and safety.

Infographic showing various Medical Device Testing job openings in Wisconsin as of July 2026, with employment types broken down into 77% Full Time, 15% Part Time, and 8% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $77,099 per year, or $37.1 per hour.
Sr. Process Development Engineer

Sr. Process Development Engineer

Cirtec Medical Corp.

Sturtevant, WI

$115K - $135K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago


Cirtec Medical rating

6.6

Company rating: 6.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz


Job description

Description

About us:

For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems.

Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team!

Position Summary:

The Sr. Engineer, Process Development position is primarily responsible for working in a functional silicone process engineering group within the department, consisting of multiple engineering disciplines. Involved in the design, development, documentation, and validation and of new customer components, and modification of existing products including defining requirements, timelines, and deliverables with a focus on prototypes, process development, design verification, engineering builds, training production, and preparation for process validation and manufacturing transfer of products.

Key Responsibilities:

  • Attends and arranges project meetings to discuss current and future design and development initiatives
  • May serve as a primary contact with clients on projects of moderate complexity.
  • Assist with preparation of proposals and quotations for clients; interface as needed to resolve questions in a timely manner.
  • Assist in preparation and maintaining of project plans to satisfy milestones, deadlines, budgets, and medical device quality regulations with required actions. Track and communicate project status, plans, issues, timelines, action items, and budgets.
  • Serve as the subject matter expert(SME) for silicone extrusion within the Cirtec Plant network.
  • Provide guidance and direction to coworkers on areas of technical expertise.
  • Troubleshoot production processes as required.
  • Evaluate and select appropriate test methods for product requirements.
  • Proficient use of statistical data analysis and DOE in process problem solving and process/product improvement.
  • Collaborate with tooling engineers and tool build center for the design, delivery of effective extrusion tooling
  • Collaborate with material science team and customer on identifying ideal silicones for component design and process optimization.
  • Responsible for the following project inputs:
    • Feasibility builds, documentation, and testing
    • Equipment selection, process development and documentation
    • Device Verification samples and testing
    • Operator training
    • Process Failure Mode Effects Analysis
    • Clinical builds
    • Process Validation
  • Involvement in the full design, development, and validation requirements of projects, including:
    • Product component design and specification creation, including extrusions, molded assemblies, and packaging.
    • Materials sourcing and equipment prototyping.
    • Process verification and validation activities, including data for regulatory submission.
    • Manufacturing transfer and support of existing product lines as applicable.
  • Reliable, consistent, and punctual attendance is an essential function of the job.

Must Have:

  • A Bachelor’s degree in a STEM engineering discipline
  • 5 years of experience in process development engineering
  • Experience in an engineering environment with mechanical, tool design, and manufacturing processes (medical device preferred).
  • Must maintain high ethical standards
  • Must demonstrate good organizational skills.
  • Ability to train new engineering employees on project engineering activities and Cirtec policies and procedures.
  • Must be able to read, write and speak fluent English.
  • Strong computer skills, including the MS Office suite and MS Project.
  • Must be able to fully interpret technical drawings, blueprints, specifications, illustrations, and written documents.
  • Strong analytical skills
  • Must be able to obtain and evaluate secondary research information.
  • Ability to learn and apply new technology.
  • Knowledge of engineering principles, technical writing, material properties, good tooling practices, and statistics.
  • Willingness to travel as needed

Salary Range: $115,000 - $135,000 / Annual

Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.

We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec’s goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Our benefits include Training and career development, Healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs, Paid Time Off and 401(k) retirement savings with a company match.


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