1

Internship R&D Engineer Medical Device Jobs in Madison, WI

Manufacturing Engineer

Madison, WI ยท On-site

$73K - $94K/yr

Manufacturing Engineer Location: Onsite - Madison, WI Pay Rate: 48-54/hr. (W2) Job Summary The ... Prior experience in a medical device manufacturing or technical support role is highly desirable.

... Engineering, or related field. * 5+ years of relevant experience in consultative sales, marketing, or product management. * Experience in specialty chemicals, polymers, or medical device industries.

The Software engineer collaborates in a complex environment integrating software with other ... Experience with Medical Device development or other regulated environments. * Experience with ...

The Software engineer collaborates in a complex environment integrating software with other ... Experience with Medical Device development or other regulated environments. * Experience with ...

Product Design Engineer, IoT

Madison, WI ยท On-site

$130K - $156K/yr

... engineering documentation, including CAD models, wiring schematics, BOMs, build protocols, and ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Product Design Engineer, IoT

Madison, WI

$130K - $156K/yr

... engineering documentation, including CAD models, wiring schematics, BOMs, build protocols, and ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Product Design Engineer, IoT

Madison, WI ยท On-site

$130K - $156K/yr

... engineering documentation, including CAD models, wiring schematics, BOMs, build protocols, and ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Product Design Engineer, IoT

Madison, WI ยท On-site

$130K - $156K/yr

... engineering documentation, including CAD models, wiring schematics, BOMs, build protocols, and ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Set your own hours and tutor as much as you'd like. * Tutor remotely using our purpose-built Live ... Skilled at breaking down physiological system modeling, biomechanical analysis, and medical device ...

... regulated medical device environment. REPORTING TO/DEPARTMENT: Reports to the Director, Systems Engineering in the Systems Engineering & Applied Science department ESSENTIAL DUTIES AND ...

... probiotics R&D. IFF is a global leader in flavors, fragrances, food ingredients, and health ... engineering, process improvement, or technical project work (academic, coop, internship, or ...

... Engineer is preferred, or any other engineering degree Must have project management experience PMP is strongly desired Must have Medical Device background Must have regulatory experience Expert in ...

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

Software Development Engineer Give hope. Give health. Make your mark in the fight against cancer ... Experience with Medical Device development or other regulated environments. * Experience with ...

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

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

next page

Showing results 1-20

Internship R D Engineer Medical Device information

See Madison, WI salary details

$11

$19

$29

How much do internship r&d engineer medical device jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for internship r&d engineer medical device in Madison, WI is $19.46, according to ZipRecruiter salary data. Most workers in this role earn between $16.25 and $21.06 per hour, depending on experience, location, and employer.

What does an Internship R&D Engineer in Medical Device do?

An Internship R&D Engineer in Medical Device assists in the research and development of new medical technologies and products. Their responsibilities typically include supporting senior engineers in designing, testing, and improving medical devices, conducting experiments, collecting and analyzing data, and preparing technical documentation. Interns also learn about regulatory standards and industry best practices while working as part of a multidisciplinary team. This role is ideal for students or recent graduates looking to gain hands-on experience in medical device innovation.

What are the key skills and qualifications needed to thrive as an Internship R&D Engineer in Medical Devices, and why are they important?

To thrive as an Internship R&D Engineer in Medical Devices, you generally need a background in biomedical engineering or a related field, with strong analytical and problem-solving abilities. Familiarity with CAD software, lab equipment, and basic knowledge of regulatory standards like ISO 13485 is important, and prior internships or relevant coursework can be advantageous. Attention to detail, effective communication, and collaborative teamwork skills help you contribute meaningfully to projects and navigate cross-functional environments. These skills ensure you can support innovative product development while adhering to strict safety and quality standards in the medical device industry.

What is the difference between Internship R&D Engineer Medical Device vs R&D Engineer Medical Device?

AspectInternship R&D Engineer Medical DeviceR&D Engineer Medical Device
QualificationsEnrolled in or recent graduate of engineering/biomedical programsBachelor's or Master's in engineering/biomedical fields
Work EnvironmentInternship programs, entry-level projects, supervised tasksFull-time, independent project work, team collaboration
ResponsibilitiesAssisting in research, testing, and documentationDesign, develop, and improve medical device products
Industry UsageCommonly used for training and entry-level experienceCore role in product development and innovation

In summary, the Internship R&D Engineer Medical Device is an entry-level position designed for students or recent graduates gaining initial industry experience. The R&D Engineer Medical Device is a full-time professional role with greater responsibilities in product development and innovation within the medical device industry.

What types of projects or tasks can an Internship R&D Engineer expect to work on in the medical device industry?

As an Internship R&D Engineer in the medical device industry, you can expect to be involved in a variety of projects such as prototyping new device concepts, conducting laboratory experiments, performing data analysis, and supporting design verification and validation activities. Interns often collaborate closely with multidisciplinary teams, including senior engineers, regulatory specialists, and clinicians, to help solve real-world problems and improve patient outcomes. This hands-on experience provides valuable insight into the product development lifecycle and offers opportunities to contribute to meaningful projects that can enhance your technical and professional skills.
What cities near Madison, WI are hiring for Internship R&D Engineer Medical Device jobs? Cities near Madison, WI with the most Internship R&D Engineer Medical Device job openings:

Manufacturing Engineer

Kellton Tech

Madison, WI โ€ข On-site

$73K - $94K/yr

Contractor

Posted 17 days ago


Job description

Job Title: Manufacturing Engineer
Location: Onsite โ€“ Madison, WI
Pay Rate: 48-54/hr. (W2)

Job Summary

The Manufacturing Engineer is responsible for providing technical guidance and support for manufacturing methods, tooling, test systems, process documentation, and equipment to ensure efficient and compliant medical device manufacturing. This role promotes continuous improvement and ensures all operations conform to internal quality systems, ISO 13485, and regulatory standards. This position involves cross-functional collaboration and direct support to production, engineering, quality, and materials teams. The ideal candidate is an experienced problem-solver with strong technical skills, project management experience, and the ability to work independently in a fast-paced, regulated environment.

Key Responsibilities

  • Own and support manufacturing processes, test systems, tooling, and documentation to ensure compliance with quality and regulatory requirements.
  • Provide process expertise and act as SME for production and process controls.
  • Train and guide production associates on new and existing processes, equipment, and documentation.
  • Troubleshoot production issues and collaborate across teams to implement cost-effective solutions.
  • Develop and revise SOPs, Work Instructions, Process Flow Diagrams, Device History Records, and validation documentation.
  • Participate in continuous improvement efforts to enhance yield, manufacturability, and efficiency.
  • Serve on the Material Review Board (MRB); investigate nonconforming devices and components.
  • Define and execute verification and validation (V&V) plans.
  • Provide inputs on manufacturing strategies, capital planning, and facility maintenance.
  • Assist with cost estimation for new products.
  • Support equipment troubleshooting and participate in supplier development initiatives.
  • Use statistical analysis and lean tools for root cause investigations and process optimization.
  • Perform other duties as needed to support operational and business objectives.

Required Qualifications

  • Education:
  • Associateโ€™s degree in Electrical or Mechanical Engineering (equivalent combination of experience, education, and training accepted).
  • Experience:
  • Experience as a Manufacturing Engineer or Engineering Technician preferred.
  • Prior experience in a medical device manufacturing or technical support role is highly desirable.
  • Technical Skills:
  • Working knowledge of ISO 13485, FDA 21 CFR regulations.
  • Proficient in MS Office (Word, Excel, etc.); SAP and LabView experience a plus.
  • Familiarity with Lean Six Sigma (Green Belt certification preferred).

Key Competencies

  • Leadership and ability to train/guide manufacturing teams.
  • Strong organizational and time management skills.
  • Effective communicator with strong interpersonal and cross-functional collaboration skills.
  • Skilled in root cause analysis, process improvements, and project execution.
  • Ability to manage multiple projects and priorities in a regulated environment.

Organizational Relationship & Scope

  • Reports to the Manufacturing Engineering/Facilities Manager.
  • Works cross-functionally with Sustaining Engineering, Global Device Engineering, QA, Regulatory, and Technical Operations.
  • Responsible for new product introduction, process optimization, and production support.

Working Conditions

  • Mix of hands-on manufacturing line support, computer-based work, and cross-functional meetings.
  • May require extended hours, weekends, or holidays with manager approval.