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Principal Device Engineer, CPD

Date: Nov 17, 2021

Location: Kfar Saba, IL, 1111

Company: Teva Pharmaceuticals

Company Info

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

  • Generate/review Risk Management File documents including User FMEA, Design FMEA, Process FMEA and material selection rational for biocompatibility.
  • Execute/participate in/coordinate R&D development activities such as design of prototypes, design of experiments, design of test fixtures, perform testing activities, draft experimental protocols and reports. Perform product and process root cause analysis and problem solving.
  • Generate/review design output documentation such as component and assembly drawings, bill of materials generation.
  • Execute/review product commercialization activities such as design or assembly, part and cost reduction including interfacing with the device manufacturer, component suppliers, and assembly equipment vendors.
  • Generate, execute, and/or review Design Verification protocols as well as write technical reports
  • Implement transfer of design to manufacture of product. Generate/review manufacturing documentation such as assembly work instruction, validation protocols and reports, batch records, and IQ OQ PQ equipment qualifications.
  • Follows Teva Safety, Health, and Environmental policies and procedures.
  • Other projects and duties as required/assigned.

Qualifications

  • University Bachelor of Science in Mechanical/Biotechnology/Quality or Biomedical Engineering -  required
  • Pharmaceutical / Medical Device industry experience, with extensive experience in medical devices -2-5 years Required
  • Process validation and manufacturing experience
  • Polymer Science and/or Injection Molding 
  • Experience in Quality and regulation of medicinal product
  • Experience in leading Risk management process
  • Ability to work in a team and on your own
  • Speak fluent English
  • The position located in Kfar Saba

Function

Research & Development

Sub Function

Drug Development and Preclinical Studies

Reports To

Sr Mgr Combination Product and Device, Device R&D Ops

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.