Intern Product Support (Austin,TX)

Smith+NephewAustin, TX
15dOnsite

About The Position

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. The R&D intern program will consist of a robust induction plan followed by a 3-month internship across various facets of our Product Support organization within the Sports Medicine and ENT Franchises at S+N. The position will be based in Austin, Texas. What will you be doing? Perform a variety of tasks daily to sustain the current portfolio of medical devices. Write and maintain detailed bills of materials, material specifications, and device drawings for a medical device. Work with Regulatory and Quality departments to assist in the expansion of medical devices into new markets all over the world. Update existing CAD specifications (3D assemblies and 2D drawings) to implement design changes. Planned Start Date: May 2026 Program Length: 3 Months Location: Austin, TX

Requirements

  • Must be currently matriculated at an accredited university as an undergraduate majoring in Mechanical or equivalent applicable engineering. (Sophomore)
  • Must be in excellent academic standing, with a 3.0 preferred
  • Demonstrated ability to work effectively in a cross-functional team environment.
  • High learning agility
  • Strong written and verbal communication and technical writing skills
  • Analytical approach to problem solving.
  • Basic understanding and experience with process documentation for use in fabrication and assembly.
  • Experience with 3-D modeling software (Solidworks) and knowledge of drafting practices, GD&T, ASME/ANSI drawing standards a plus.

Nice To Haves

  • Previous applicable intern, co-op, part-time or apprenticeship experience is preferred
  • Experience with 3-D modeling software (Solidworks) and knowledge of drafting practices, GD&T, ASME/ANSI drawing standards a plus.

Responsibilities

  • Perform a variety of tasks daily to sustain the current portfolio of medical devices.
  • Write and maintain detailed bills of materials, material specifications, and device drawings for a medical device.
  • Work with Regulatory and Quality departments to assist in the expansion of medical devices into new markets all over the world.
  • Update existing CAD specifications (3D assemblies and 2D drawings) to implement design changes.
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