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Intern - Device Engineering

Date: Nov 9, 2022

Location: Salt Lake City, US, 0000

Company: Teva Pharmaceuticals

Who are we?

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

 

Embark on a future with an international pharmaceuticals company, contributing your creative energy to high-impact projects from the moment you arrive through the course of this 14-week experience. You will take part in meaningful work and real-life projects that will help you grow both professionally and personally throughout the program. 

 

Location:  (Salt Lake City, Utah) 
Length: 14 weeks (5/8/23-8/11/23)
Schedule: You must be available to work a 40-hour work week for 14 weeks summer 2023
Pay:  ($23.00/hr) 

 

Tasks & responsibilities
As a Device Development Engineering Intern in Teva's SLC R&D Devices group, you will participate in the design, development, verification and validation of combination products  (drug + device) in support of Teva’s global R&D pipeline with special focus on transdermal pharmaceuticals.  You will gain knowledge of the regulations, directives, guidelines and standards relevant to the combination products on which you contribute. You will be exposed to a global team of combination products developers who are motivated by the opportunity to have a positive impact on patient’s lives.

 

Essential Duties & Responsibilities:

  • Lead the design and development of mechanical test fixtures
  • Develop and execute mechanical test methods to verify device performance on exhibit batches
  • Participate in range finding builds as needed, and execute testing
  • Create or modify SolidWorks models and drawings 
  • Perform statistical analysis on collected data
  • Author technical documents such as test protocols and final reports
  • Assist in product and process root cause analysis and problem solving

Qualifications

 

  • Currently enrolled in as a Junior level or above in a Bachelors Degree program majoring in Mechanical, Biomedical, or Chemical Engineering.  
  • Fundamental understanding and experience in Design Controls, Medical Devices, and Mechanical Testing for Design Verification
     

Function

Administration

Sub Function

Administrative Services

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.