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Engineering Medical Device Jobs in Wisconsin (NOW HIRING)

Engineering Manager

Kenosha, WI ยท On-site

$110K - $130K/yr

The Engineering Manager will play a critical role in developing advanced machining strategies ... Knowledge of materials, tooling, and medical device manufacturing processes. * Strong understanding ...

Quality Engineering Technician

Hudson, WI ยท On-site

$21 - $30/hr

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 ...

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 ...

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 ...

Industry: Healthcare/Medical device Title: Engineering project manager Location: Madison, WI 53718 Qualifications Critical Needs: BS Mechanical Engineer is preferred, or any other engineering degree ...

Showing results 21-40

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.

Medical Device Quality Inspector

Kellton Tech

Madison, WI โ€ข On-site

$30/hr

Contractor

Re-posted 23 days ago


Job description

Job Title: Medical Device Quality Inspector
Location: Madison, WI (Onsite)
Pay Rate: $30/hr. on W2

Job Summary

The Medical Device Quality Inspector is responsible for ensuring that materials, processes, and activities involved in daily device manufacturing, processing, and packaging meet current Good Manufacturing Practices (GMP) and comply with ISO 13485 and applicable quality standards. This position plays a key role in maintaining the quality integrity of medical device products through precise inspection and documentation.

Key Responsibilities

  • Inspect parts according to engineering drawings and specifications.
  • Perform dimensional inspections using precision tools such as calipers, micrometers, gage pins, plug gages, and thread gages.
  • Record acceptance data in the SAP ERP system after inspection.
  • Enter failure data into nonconforming material reports (NCMRs) when applicable.
  • Support daily production activities and collaborate with the team to meet quality and output goals.
  • Follow all established procedures in compliance with FDA and ISO 13485:2008 standards.
  • Maintain documentation in accordance with GMP and company policies.
  • Adapt to various inspection assignments and assist team members as needed.
  • Work overtime when required based on production schedules and incoming part volumes.

Desired Experience

  • Experience with optical measurement machines or a Coordinate Measuring Machine (CMM).
  • Familiarity with ISO 13485 or ISO 9001 quality management systems.
  • Prior experience with material or component inspection in a regulated environment preferred.
  • Exposure to computer-based quality systemsSAP experience is a plus (training provided).

Qualifications

  • Education: High School Diploma or equivalent.
  • Language: Ability to read and write in English.
  • Mathematical Skills: Basic math proficiency required.
  • Technical Skills:
  • Ability to use precision measurement tools such as calipers, micrometers, and thread gages.
  • Proficiency with Microsoft Word and Excel.
  • Soft Skills:
  • Strong attention to detail and defect identification.
  • Ability to work efficiently in a fast-paced team environment with minimal supervision.
  • Flexibility to work overtime as required.

About the Role

This is a hands-on quality inspection position within a team-oriented environment that supports manufacturing operations. The ideal candidate is detail-orientedcomputer-proficient, and eager to learn inspection procedures under regulated (FDA and ISO 13485) conditions.