Quality Assurance Intern

Marmon Holdings, Inc.Charlottesville, VA
Onsite

About The Position

MicroAire Surgical Instruments LLC, a part of the global industrial organization Marmon Holdings (backed by Berkshire Hathaway), is seeking a Quality Assurance Engineering Intern for Summer 2026. This internship offers the opportunity to assist the QA Department with various critical tasks within the medical device industry. The intern will gain experience in labeling changes and improvements, including new software implementation, change order processing, label first article inspections, and working with operations. They will also be involved in updating the European EUDAMED medical device database, improving documentation and change orders (including SolidWorks updates), and updating Endotine QMS. The role includes supporting design control documentation for New Product Development, updating legacy DHF documentation, and assisting with quality and process improvements, such as process validations and other manufacturing requirements. The intern will also understand and assist with Quality Assurance Engineering (QAE) activities like nonconformances, CAPAs, and complaints, as well as assist with verification activities for product changes. This internship is ideal for an Engineering student interested in quality assurance related to product design and manufacturing in the medical device sector.

Requirements

  • Currently pursuing an Engineering degree.
  • Interest in quality assurance related to product design and manufacturing within the medical device industry.

Nice To Haves

  • SolidWorks experience

Responsibilities

  • Assist with new labeling software implementation, including processing Change Orders, Label First Article Inspections, and working with Operations on planning/execution.
  • Update the European EUDAMED medical device database with 2026 requirements.
  • Support documentation improvements and change orders, including SolidWorks updates.
  • Assist with Endotine QMS updates.
  • Provide support for Design Control documentation for New Product Development.
  • Update legacy DHF documentation.
  • Assist with Process Validations and other manufacturing requirements associated with process improvements.
  • Understand and assist with QAE activities such as nonconformances, CAPAs, and complaints.
  • Assist with Verification activities associated with product change(s).

Benefits

  • Hourly rate compensation
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service