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Intern, R&D - Vascular Access in Marlborough, MA at Angiodynamics, Inc.

Date Posted: 3/9/2018

Job Snapshot

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Job Description

AngioDynamics provides benefits to patients by being the leader in design, development, manufacturing and marketing of innovative, proprietary, therapeutic devices used by interventionalists and surgeons for the minimally invasive treatment of peripheral vascular disease, tumor therapy and other, non-vascular diseases. Our 6-month internship will give interns a project based learning experience that will strive to build your understanding of how a medical device business operates, enhance your skillset and grow your network. This internship will provide practical, professional experience for the college student while contributing to the overall goals of the Vascular Access (VA) Research & Development (R&D) Engineering team.

Work with the Vascular Access R&D engineering team on daily task on high priority projects. These tasks include but are not limited to hands-on testing of medical devices, develop test methods, test fixtures, product specifications, and technical reports. The candidate will attend project meetings and work with cross functional teams to gain experience in the development process of medical devices. The intern will assume a primary role in projects working either independently or as part of a team, as well as perform other activities that will support the over all objectives of the area they are assigned to.
  • Technical and analytical writing.
  • Creative thinking regarding problem solving and rationale writing.
  • Work on projects that will help develop analytical, audit, research, testing and validation skills.
  • Attend and participate in department meetings.
  • Develop and maintain documentation and forms.
  • Use Excel, Word, Project Management, or Visio to create correspondence, spreadsheets, forms, graphs, flowcharts, basic skills in Solidworks etc.
  • Provide customer service to the department’s internal and external customers.
  • Ensure compliance with all relevant quality and regulatory/legal requirements.
  • Other duties as assigned by the supervisor.