R&D Engineering Intern (Medical Devices)

CordisIrvine, CA
3h$23Onsite

About The Position

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs. We are seeking a highly motivated R&D Engineering Intern to support the research, design, and development of innovative medical devices. This role offers hands-on experience in early-stage product development, prototyping, and testing within a regulated medical device environment. The intern will work closely with cross-functional teams to help translate user needs and design concepts into functional prototypes and validated designs that improve patient outcomes.

Requirements

  • Currently pursuing a Bachelor’s or Master’s degree in Engineering (Biomedical, Mechanical, Electrical, or related field)
  • Strong interest in product development and medical device innovation
  • Solid problem-solving and analytical skills
  • Ability to communicate technical concepts clearly, both written and verbal
  • Comfortable working in a lab environment and handling physical prototypes
  • Proficiency with Microsoft Office tools

Nice To Haves

  • Experience or coursework in medical device design, biomechanics, or product development
  • Familiarity with CAD software (e.g., SolidWorks, Creo)
  • Exposure to prototyping methods such as 3D printing, machining, or electronics assembly
  • Basic understanding of FDA design controls or ISO 13485
  • Experience with data analysis tools (MATLAB, Minitab, Excel)

Responsibilities

  • Assist with the design and development of medical device concepts, components, and subsystems
  • Support prototype fabrication, assembly, and iteration using lab and shop equipment
  • Conduct bench testing, experiments, and data collection to evaluate design performance
  • Analyze test data and document results in technical reports and presentations
  • Assist in creating and maintaining R&D documentation, including design inputs, design outputs, and verification test protocols
  • Collaborate with Quality, Regulatory, and Manufacturing teams to ensure designs meet requirements and are manufacturable
  • Support troubleshooting and root cause analysis of design or test failures
  • Follow design control processes, quality system procedures, and laboratory safety practices

Benefits

  • Hands-on experience in R&D for regulated medical device products
  • Exposure to the full design lifecycle—from concept through verification
  • Mentorship from experienced R&D engineers and technical leaders
  • Experience working with cross-functional teams in a real-world product development setting
  • The opportunity to contribute to products that improve patient health and quality of life
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