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Intern - Design Assurance Engineer (Summer 2027)

Plexus Corp
Raleigh, USA
Full-time
Intern
Onsite
Discovered 2 weeks ago

Full Job Posting

RESPONSIBILITIES

  • Ensure that the planned project activities are compliant with Plexus' Standard Operating Procedures, ISO (i.e. 13485) quality systems, FDA Quality System Regulations (QSR), REACH and RoHS directives, and medical device standards (i.e. IEC 60601) as applicable for each unique product.
  • Direct the development and assembly of prototypes by authoring and reviewing product documentation in accordance with quality and change management procedures and guidelines. Provide documentation and technical assistance to design engineering staff and material procurement team to ensure high quality prototypes are built in a timely manner.
  • Participate in the Plexus quality system development and maintenance.
  • Demonstrate proficiency using lab equipment and debug techniques to ensure electro-mechanical products meet design requirements.
  • Determine appropriate specifications to comply with regulatory and compliance requirements of intended markets, and facilitate documentation of such specifications.
  • Lead the development of the product Risk Management Plan, Design Failure Modes and Effects Analyses, and Fault Tree Analyses as necessary to comply with ISO 14971 requirements.
  • Participate in all Design Verification test activities, including generation of the Verification Plan, Procedures, Traceability Matrix, and Report documents, as well as prototype test execution.
  • Evaluate a product’s Bill of Materials to determine any lifecycle or environmental compliance concerns and investigate alternative solutions to meet the project needs.

MINIMUM QUALIFICATIONS

  • Student working toward a Bachelor’s degree in Computer Engineering, Electrical Engineering, Biomedical Engineering, or Software Engineering for entire duration of internship.

PREFERRED QUALIFICATIONS

  • Sophomore or Junior level status
  • GPA: 3.0 or higher is preferred
  • Working knowledge of medical device and similar safety standards (i.e. IEC 60601-1, IEC 61010-1)
  • Understanding of regulatory requirements
  • This document does not represent a contract of employment and is not intended to capture every possible assignment the incumbent could be asked to perform.
  • We are pleased to provide reasonable accommodations to individuals with disabilities or special requirements. If you need an application accommodation, please contact us by email at [email protected]. Please include your contact information and clearly describe how we can help you. This email is for accommodation requests only and cannot be used to inquire about the status of applications.
  • We are an Equal Opportunity Employer (EOE) and do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
  • Some offers of employment are contingent upon successfully passing a drug screen and/or background check.

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