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Biomedical Device Engineer Jobs in Wisconsin (NOW HIRING)

Smiths Machine

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 ...

ARCH Global Precision

Quality Engineer II

Kenosha, WI · On-site

$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 ...

Actalent

Design Engineer

Kenosha, WI

$38.46 - $48.07/hr

Ensure all designs align with medical device standards and internal quality expectations ... Bachelor's degree in mechanical engineering or biomedical engineering is preferred. * Equivalent ...

Medline

Validation Engineer

Hartland, WI

$73K - $110K/yr

Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering. * Six Sigma certification. * 3 years of validation experience in a cGMP Device ...

Medline

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering. * Six Sigma certification. * 3 years of validation experience in a cGMP Device ...

Medline

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering. * Six Sigma certification. * 3 years of validation experience in a cGMP Device ...

Danaher

Software Engineer Internships

Kenosha, WI

... medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering (with ...

Danaher

Software Engineer Internships

Madison, WI

... medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering (with ...

Danaher

Software Engineer Internships

Racine, WI

... medical device regulatory processes Who This Is For * Students graduating in 2025 or later with a Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering (with ...

Automated Systems, Inc.

Be Seen First

Process Engineer

Madison, WI · On-site

$65 - $85/hr

... Biomedical Engineering, Industrial Engineering, or a related technical discipline. * Engineering experience in a pharmaceutical, biotech, API, medical device, food, or similarly regulated ...

Merz North America

BioProcess Engineer II

Racine, WI · On-site

... medical device environment. This role manages process and equipment implementation projects ... S.) in Biomedical Engineering, Mechanical Engineering, Chemical Engineering, or Physical Science ...

Merz North America

BioProcess Engineer II

Racine, WI

... medical device environment. This role manages process and equipment implementation projects ... S.) in Biomedical Engineering, Mechanical Engineering, Chemical Engineering, or Physical Science ...

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Showing results 1-20

All JobsBiomedical Device Engineer JobsBiomedical Device Engineer Jobs in Wisconsin

Biomedical Device Engineer information

See Wisconsin salary details

$41.4K

$95.7K

$141.3K

How much do biomedical device engineer jobs pay per year?

As of Jun 14, 2026, the average yearly pay for biomedical device engineer in Wisconsin is $95,694.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,200.00 and $117,100.00 per year, depending on experience, location, and employer.

What are biomedical device engineers?

Biomedical device engineers are professionals who design, develop, test, and maintain medical devices and equipment used in healthcare. Their work bridges the fields of engineering, biology, and medicine to create technologies that improve patient care, such as prosthetics, imaging machines, and diagnostic tools. They collaborate with medical professionals to ensure devices are safe, effective, and meet regulatory standards. Biomedical device engineers may also be involved in research, product development, and troubleshooting equipment in clinical settings.

What is the difference between Biomedical Device Engineer vs Biomedical Equipment Technician?

AspectBiomedical Device EngineerBiomedical Equipment Technician
CredentialsBachelor's degree in biomedical engineering or related fieldAssociate's degree or certification in biomedical technology
Work EnvironmentDesign, develop, and test medical devices in labs or officesInstall, maintain, and repair medical equipment in hospitals or clinics
Industry UsageUsed by medical device companies, research institutions, and hospitalsPrimarily employed by healthcare facilities and service providers

Biomedical Device Engineers focus on designing and developing new medical devices, while Biomedical Equipment Technicians handle the installation, maintenance, and repair of existing equipment. Both roles require technical knowledge, but their daily tasks and work environments differ significantly.

What are the key skills and qualifications needed to thrive as a Biomedical Device Engineer, and why are they important?

To thrive as a Biomedical Device Engineer, you need a solid background in biomedical engineering, mechanical or electrical engineering, and a bachelor's or master's degree in a related field. Familiarity with CAD software, medical device regulations (such as FDA or ISO standards), and prototyping tools is crucial. Strong problem-solving abilities, attention to detail, and effective collaboration and communication skills help you innovate and work efficiently with multidisciplinary teams. These competencies ensure the safe, effective, and compliant development of medical devices that improve patient outcomes.

What are some common challenges Biomedical Device Engineers face when working on cross-functional teams?

Biomedical Device Engineers frequently collaborate with professionals from various disciplines, including clinicians, software developers, and regulatory experts. A common challenge is aligning the technical requirements of device design with clinical needs and strict regulatory standards. Effective communication and adaptability are essential, as team members may have differing priorities or levels of technical understanding. Overcoming these challenges often leads to innovative solutions and a more robust final product, making strong teamwork and problem-solving skills invaluable in this role.
What cities in Wisconsin are hiring for Biomedical Device Engineer jobs? Cities in Wisconsin with the most Biomedical Device Engineer job openings:
Biomedical Device Engineer jobs near you
Infographic showing various Biomedical Device Engineer job openings in Wisconsin as of June 2026, with employment types broken down into 79% Full Time, 14% Part Time, and 7% Contract. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $95,694 per year, or $46 per hour.

Quality Engineer II

Smiths Machine

Kenosha, WI

$70K - $90K/yr

Full-time

Posted 5 days ago

Job description

Primary Responsibilities

• Self-starter, working independently on assigned projects, leading the team and collaborating with other internal and external parties.
• Plans, coordinates, and directs quality control programs designed to ensure continuous production of products consistent with established FDA and ISO standards.
• Investigates and addresses customer complaints (CAPA) regarding quality.
• Assists with internal/external audits of the Quality Management System (QMS) to ensure compliance to procedural, customer, and regulatory requirements.
• Fully versed in Document Control processes and procedures.
• Assists in reviewing and revising processes within the QMS (Quality Management System).
• Provides inspection activity for products throughout the production cycle.
• Creates, implements, updates and maintains work instructions, partnering with the Engineering and other departments.
• Creates and directs process/equipment validations (IQ, OQ, PQ).
• Reviews customer contracts (purchase orders, regulatory requirements, blueprints).
• Creates PPAP documentation (GR&R, control plans, first article inspection, criteria, etc.).
• Directs workers engaged in inspection and testing activities to ensure continuous control over materials, facilities, and products.
• Trains quality and other departments to achieve quality standards (visual and dimensional).
• Works with suppliers to ensure quality of all purchased parts for company use.
• Helps reduce scrap/waste, cost, time; drives for continuous improvement.
• Reliable, timely, ethical and consistent attendance.
• Travels to another facility and/or customer/vendor sites based on company needs.
• Other duties as assigned.

Qualifications

  • 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 manufacturing industry and in the quality engineering role, and/or training,
  • or equivalent combination of education and experience.
  • Knowledge of the medical device manufacturing industry is highly preferred.
  •  Experience with CNC machining and mechanical inspection is preferred.
  • Knowledge of ISO 13485 Quality Management System & FDA 21CFR 820 Regulations.
  • Knowledge of Geometric Dimensioning and Tolerancing per ASME Y14.5M.
  • Familiarity with test methods and standards for the design, verification, and validation of medical device products.

Language Ability
Ability to read, analyze, and interpret common scientific and technical manuals, training materials, financial reports, and legal documents (specifically in English). Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community (specifically in English). Ability to communicate effectively with tact, respect and professionalism within all levels of the organization. Must work responsibly with or without supervision using effective communication skills; able to collaborate with various departments and all levels of team members.

Computer Skills
To perform this job successfully, an individual should have professional and working knowledge of Microsoft office and its applications (Word, Excel, Power Point, etc.), e-mail, communication platforms (Zoom, Teams). Knowledge of manufacturing software and ERP systems (EPICOR is strongly preferred).

Certificates and Licenses
No certifications required. Relevant certifications demonstrating applied understanding of medical device quality system requirements, such as AAMI Quality System, Certified ASQ or ISO Lead Auditor and Regulatory Affairs Professional Society (RAPS) preferred. GD&T certifications are highly preferred.

Managing Responsibilities
No direct reports.

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