Intern (Disposables Engineering)

Nordson Corporation•Allen, TX

About The Position

Nordson Medical, a global leader in Interventional Solutions, Fluid Components, and Surgical Solutions, is seeking an experienced and highly motivated individual to join our team. We are committed to creating a diverse and inclusive workplace, and we are looking for candidates who share that same commitment. As a member of our team, you will have the opportunity to work in a dynamic and collaborative environment, where your ideas and contributions will be valued and respected.

Requirements

  • Pursuing a Bachelor’s degree in Mechanical, Industrial, Manufacturing, Biomedical Engineering, or related field.
  • Strong organizational and time management skills with the ability to independently complete assigned tasks.
  • Strong interest in medical device manufacturing and continuous improvement.
  • Effective written and verbal communication skills.
  • Detail-oriented and self-motivated with the ability to follow directions and ask questions.
  • Familiarity with Microsoft Office (Word, Excel, PowerPoint); exposure to SolidWorks or CAD is preferred.
  • Basic understanding of root cause analysis, data analysis, and engineering documentation.

Nice To Haves

  • Previous internship, co-op, or project experience in regulated manufacturing or medical device environment is a plus.

Responsibilities

  • Assist in sustaining manufacturing processes by supporting troubleshooting, documentation, and continuous improvement activities.
  • Support execution of validation and qualification protocols (IQ/OQ/PQ) for equipment, processes, and design changes.
  • Collaborate with engineers to identify and implement process improvements that enhance safety, quality, and throughput.
  • Participate in engineering change order (ECO) documentation, test execution, and implementation activities.
  • Help analyze production data, perform basic statistical analysis, and summarize findings in reports.
  • Observe and participate in root cause analysis activities and nonconformance investigations.
  • Learn and apply Lean and Six Sigma principles to reduce waste and improve efficiency.
  • Participate in design reviews and contribute DFM (Design for Manufacturability) input under guidance.
  • Assist in drafting technical documents, validation plans, and troubleshooting guides.
  • Learn quality and regulatory standards applicable to medical devices, including FDA QSR and ISO 13485.
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