Intern - Manufacturing Engineer

OrthofixLewisville, TX
12h

About The Position

Why Orthofix? Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the unrivaled partner in Med Tech. Our global team of over 1,600 employees brings to market highly innovative, cost-effective, and user-friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people’s lives? Look no further. JOB PURPOSE The primary objective of this Internship is to support the Manufacturing Engineering team at Orthofix Biologics, Irvine site by assisting with day-to-day production support tasks, performing manufacturing line assessments, taking ownership of assigned tasks within long-term projects, and implementing continuous improvements through collaboration with Engineering, Operations and Quality Engineering departments. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES The following are the essential functions of this position. This position may be responsible for performing additional duties and tasks as needed and assigned.

Requirements

  • HS Diploma or equivalent required
  • Enrollment in Bachelor’s or Master’s degree program in Mechanical Engineering and/or Biomedical Engineering
  • Junior, Senior, or Graduate student level
  • 3.0 GPA
  • Foundational experience with CAD software
  • Mechanical Design Experience
  • Strong problem-solving skills

Nice To Haves

  • Machine shop experience
  • Controlled documents system experience
  • Functional experience with CAD Software, preferably SolidWorks

Responsibilities

  • Lead, support, and facilitate communication and problem-solving between Engineering, Operations and Quality Engineering.
  • Collaborate on process improvement initiatives and provide support through validation activities as needed.
  • Maintain meticulous documentation to ensure adherence to site and regulatory standards.
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