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6 дней назад

Intern (Disposables Engineering)

Формат работы
onsite
Тип работы
fulltime
Грейд
trainee
Английский
b2
Страна
US
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Описание вакансии

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TL;DR
Intern (Disposables Engineering) (Medical Devices): Supporting medical-device manufacturing processes, validation activities, engineering documentation, and continuous improvement with an accent on process troubleshooting, quality compliance, and production efficiency. Focus on analyzing production data, participating in root cause investigations, applying Lean and Six Sigma principles, and supporting IQ/OQ/PQ qualification activities.

Location: Allen, Texas, United States; onsite

Company

Nordson Medical designs, develops, and manufactures complex medical devices and component technologies for interventional, fluid management, and surgical applications.

What you will do

  • Support manufacturing process troubleshooting, documentation, and continuous improvement activities.
  • Assist with validation and qualification protocols, including IQ/OQ/PQ, for equipment, processes, and design changes.
  • Collaborate with engineers on process improvements targeting safety, quality, throughput, and waste reduction.
  • Participate in engineering change orders, testing, design reviews, and Design for Manufacturability activities.
  • Analyze production data, perform basic statistical analysis, and prepare technical reports and troubleshooting guides.
  • Observe and support root cause analyses and nonconformance investigations.

Requirements

  • Must be based at the Allen, Texas site.
  • Pursuing a bachelor's degree in mechanical, industrial, manufacturing, biomedical engineering, or a related field.
  • Basic understanding of root cause analysis, data analysis, and engineering documentation.
  • Strong organizational, communication, time management, and independent task-completion skills.
  • Familiarity with Microsoft Office; SolidWorks or CAD exposure is preferred.
  • Ability to learn and apply medical-device quality and regulatory standards, including FDA QSR and ISO 13485.

Nice to have

  • Previous internship, co-op, or project experience in regulated manufacturing or medical devices.
  • Exposure to SolidWorks or CAD.

Culture & Benefits

  • Full-time opportunity in a dynamic and collaborative engineering environment.
  • Supportive, inclusive, and diverse workplace.
  • Opportunities to develop skills in medical-device manufacturing, quality, and continuous improvement.
  • Career development and advancement support through investment in employee skill building.

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