ZipRecruiter

Log In

2

Entry Level Medical Device Engineer Jobs in Wisconsin

MGS Mfg. Group, Inc

Quality Engineer

Richfield, WI · On-site

$71K - $92K/yr

As a Quality Engineer at MGS, you will assist with the development of quality systems, procedures ... Approve Medical Device release for shipment, as required. * * Perform batch record reviews for ...

Kellton

Software Engineer Opportunity

Madison, WI · On-site

Hi - My direct client is looking for a Software Engineer. If you're interested, please email me ... Experience in medical device or FDA‑regulated industries. * Knowledge of data integrity rules ...

MGS Mfg. Group, Inc

Quality Engineer

Richfield, WI

$71K - $92K/yr

As a Quality Engineer at MGS, you will assist with the development of quality systems, procedures ... Approve Medical Device release for shipment, as required. * * Perform batch record reviews for ...

MPE-Inc

Manufacturing Engineer Fabrication

Sturtevant, WI · On-site

$85K - $95K/yr

As our Manufacturing Engineer, Fabrication, you'll design and optimize the metal fabrication ... medical device assemblies. This isn't a "shadow someone for a year" role: with 2+ years of process ...

SEEK Careers Staffing

Production Operator

Baldwin, WI · On-site

$19 - $21/hr

... Entry Level Join a Growing Leader in Medical Plastics Manufacturing! Are you seeking a company ... Previous experience in plastics or medical device manufacturing is a plus, but not required -- we ...

Actalent

Quality Engineer

Milwaukee, WI

$70K - $91K/yr

Quality Engineer The Quality Engineer evaluates and investigates product complaints and ... Exposure to medical device or GMP-related industries, with understanding of regulated quality ...

Actalent

Quality Engineer

Milwaukee, WI · On-site

$70K - $91K/yr

Quality Engineer The Quality Engineer evaluates and investigates product complaints and ... Exposure to medical device or GMP-related industries, with understanding of regulated quality ...

Accuray Incorporated

Software Engineer

Madison, WI · On-site

Contribute to sustaining engineering by troubleshooting, participating in root-cause analysis, and ... Experience with Medical Device development or other regulated environments. * Experience with ...

Accuray

Software Engineer

Madison, WI

Contribute to sustaining engineering by troubleshooting, participating in root-cause analysis, and ... Experience with Medical Device development or other regulated environments. * Experience with ...

ACCURAY

Software Engineer

Madison, WI · On-site

Contribute to sustaining engineering by troubleshooting, participating in root-cause analysis, and ... Experience with Medical Device development or other regulated environments. * Experience with ...

Superbeo

Supplier Quality Associate

Sturtevant, WI · On-site

Requirements: * BS/BA in Physical Science or Engineering or 2 + years in medical device/Pharmaceutical industry * Recent graduates encouraged to apply. * Experience in Quality Assurance and/or other ...

previous page

Showing results 41-60

All JobsMedical Device Engineer JobsEntry Level Medical Device Engineer JobsEntry Level Medical Device Engineer Jobs in Wisconsin

Entry Level Medical Device Engineer information

See Wisconsin salary details

$14

$31

$51

How much do entry level medical device engineer jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for entry level medical device engineer in Wisconsin is $31.61, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $34.95 per hour, depending on experience, location, and employer.

What does an entry level medical device engineer do?

An entry level medical device engineer assists in designing, developing, and testing medical devices such as implants, diagnostic equipment, or surgical tools. They often work as part of a team under the supervision of experienced engineers, ensuring products meet regulatory standards and function safely and effectively. Responsibilities may also include documenting results, conducting research, and supporting manufacturing or quality assurance processes. This role provides hands-on experience with engineering principles in the healthcare industry and often serves as a starting point for more specialized or senior positions.

What is the difference between Entry Level Medical Device Engineer vs Quality Assurance Technician?

AspectEntry Level Medical Device EngineerQuality Assurance Technician
Required CredentialsBachelor's in engineering, biomedical or related fieldBachelor's in science, engineering, or related field; certifications optional
Work EnvironmentDesign labs, manufacturing facilities, R&D teamsManufacturing plants, quality control labs
Employer & Industry UsageMedical device companies, biotech firmsManufacturers, healthcare device companies

Entry Level Medical Device Engineers focus on designing and developing medical devices, while Quality Assurance Technicians ensure products meet quality standards. Both roles are essential in the medical device industry and often work closely to ensure product safety and compliance.

What types of projects and responsibilities can an entry level medical device engineer expect during their first year on the job?

As an entry level medical device engineer, you can expect to work closely with cross-functional teams—including design, quality, and manufacturing—to support product development and improvements. Your responsibilities may include assisting in prototyping, conducting testing and data analysis, and maintaining detailed documentation to ensure regulatory compliance. You’ll likely gain hands-on experience troubleshooting devices, collaborating in design reviews, and participating in validation activities. This role provides an excellent foundation for learning industry standards and building technical and teamwork skills essential for career advancement.

What are the key skills and qualifications needed to thrive as an entry level medical device engineer, and why are they important?

To thrive as an Entry Level Medical Device Engineer, you need a bachelor's degree in biomedical, mechanical, or electrical engineering, along with a solid understanding of engineering principles and medical device regulations. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO standards is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help you stand out in this role. These competencies are critical for ensuring the safe design and development of innovative medical devices that meet regulatory standards and patient needs.
More about Entry Level Medical Device Engineer jobs

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

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

What are popular job titles related to Entry Level Medical Device Engineer jobs in Wisconsin?

For Entry Level Medical Device Engineer jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Entry Level Medical Device Engineer jobs in Wisconsin look for?

The top searched job categories for Entry Level Medical Device Engineer jobs in Wisconsin are:

What cities in Wisconsin are hiring for Entry Level Medical Device Engineer jobs?

Cities in Wisconsin with the most Entry Level Medical Device Engineer job openings:

Entry Level Medical Device Engineer jobs near you
Infographic showing various Entry Level Medical Device Engineer 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, with an average salary of $65,739 per year, or $31.6 per hour.

Quality Engineer

MGS Mfg. Group, Inc

Richfield, WI • On-site

$71K - $92K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Job description


MGS has an exciting opportunity for a Quality Engineer to join our MGS Richfield Manufacturing team.
As a Quality Engineer at MGS, you will assist with the development of quality systems, procedures and controls to ensure that all medical products consistently meet performance and quality specifications in the Germantown Manufacturing facility. The Quality Engineer is a leader and strong technical resource who quickly and effectively resolves quality problems with internal and external customers and suppliers.
Below are additional duties and responsibilities:
  • Generates, communicates, and implements ideas and solutions.
  • Demonstrates accuracy and thoroughness in completing tasks timely.
  • Looks for ways to improve and promote quality.
  • Monitor Corrective Action System (i.e. Customer Complaints, Supplier, Internal)
    • Initiate and investigate Customer Complaints according to MGS internal procedure and standards.
    • Record essential information on internal and/or customer-specific documentation, including updating customer portals.
    • Perform investigations using Lean, Six Sigma, and statistical methods to support root cause analysis and corrective actions.
    • Identify gaps and/or trends in systems or processes.
    • Initiate and facilitate the Corrective/Preventative Action process using the appropriate quality tools and input from subject matter experts (SME) to implement sustainable solutions.
    • Update Quality documents according to MGS Change Control procedures, as required.
    • Verify corrective action effectiveness.
  • Drive Non-Conformance Process
    • Evaluate and investigate suspect non-conforming product identified by manufacturing and/or the Quality Lab.
    • Initiate containment activities, as necessary, with Customer Service and Shipping Department.
    • Recommend disposition of product based on thorough investigation and data-driven feedback.
    • Initiate and assist Customer Service with Return Material Authorization (RMA) process.
    • Develop re-inspection, sort, and/or rework instructions for Manufacturing Operators, as required.
    • Collaborate with customer on issuing waiver or deviation documentation and obtain customer approval, as required.
  • Maintain the Quality Management System (QMS).
    • Understand ISO 13485 Quality management systems requirements.
    • Ensure continuing compliance to both internal MGS processes as well as requirements imposed upon MGS by certification bodies, regulatory agencies, and specific customer requirements.
    • Assist in internal, 2nd party, and 3rd party audits.
    • Assist with responses and corrective actions for audit findings.
  • Support Product Realization process
    • Participate in design review, process planning, and failure mode analysis
    • Provide input on evaluation of Key Product Characteristics.
    • Provide input on gaging methods and equipment.
    • Interpret customer requirements including complex blueprints and GD&T call-outs.
  • Review and approve Engineering Change Notifications and Verifications
    • Evaluate for feasibility and implement updates to customer requirements into associated product control plans, pFMEA, Inspection documentation and other related documents.
      • Incorporate industry standard best practices.
      • Incorporate MGS lessons learned.
    • Evaluate, submit and track Supplier Change Notices to customers and/or suppliers.
    • Any other duties as assigned.
    • Manufacturing point of contact for the review and disposition of product quality related questions.
  • Approve Medical Device release for shipment, as required.
    • Perform batch record reviews for medical device prior to release for shipment.
    • Generate Certificate of Analysis, as required.
    • Release product in ERP system based on customer and MGS process requirements.
  • Support Manufacturing process
    • Train Manufacturing and Quality Control personnel on customer requirements, inspection techniques, lessons learned, and rework instructions.
    • Manage product inspection and testing activities.
    • Obtain customer approvals for all required changes based on Quality Agreements.
    • Compile supporting measurement and process performance data, as necessary
    • Assemble supporting documentation package and review for completeness and accuracy
    • Review and approve production documentation updates according to MGS Engineering Change Order process.

About MGS
As a global provider of healthcare manufacturing solutions, MGS provides the right balance to drive vital innovations: robust end-to-end solutions combined with the strong customer focus and seamless collaboration of an agile partner. That's why we're the engineering and manufacturing partner of choice for today's leading Pharma, Diagnostic and MedTech innovators. Serving customers from 12 strategically located facilities around the world, we transform our customers' most pressing challenges into innovations that improve lives. To learn more about MGS, please visit www.mgsmfg.com.
Experience and Skills
A qualified Quality Engineer candidate would fulfill these requirements:
  • BS in Engineering, Quality, or related technical field is preferred.
  • Experience in a quality engineering role within a regulated manufacturing environment (medical device a plus).
  • Understanding of quality standards and regulatory requirements: ISO 9001, ISO 13485, 21 CFR Part 820.
  • Understanding of best practices for cleanroom gowning and cleanliness requirements for manufacturing within a cleanroom.
  • Experience with Microsoft Office products - Excel, Word, PowerPoint
  • Greenbelt Certification is a plus.
  • Demonstrated experience in driving continuous improvement projects and using quality tools (e.g., DMAIC, 8D, PFMEA, SPC, MSA, DOE).
  • Excellent interpersonal, communication, and presentation skills.
  • GD&T experience is a plus.

Job Benefits
We offer an excellent benefits package including medical, dental, vision, 401K, disability, life, FSA, vacation, and holidays.

Apply