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!

As a Development Engineer II you will work in the R&D organization and be responsible for design, development, implementation, and analysis of medical devices and combination products predominantly in the injectable space. You will perform engineering design evaluations and may develop a range of products including prefilled syringes, auto injectors and large volume injector systems identifying functional problems and suggest solutions. You have a working knowledge of commonly-used concepts, practices, and procedures within the medical device field relying on instructions and pre-established guidelines but is also proactive in performing the functions of the job. A development engineer will work under moderate supervision.

Responsibilities

• Present information and data to technical and management teams
• Perform Use Related Risk Analysis including but not limited to Use Failure Mode and Effects Analyses and Use Task Analyses.
• Create and maintain documentation and design history according with Teva design and quality control system, ensuring compliance to relevant standards and regulations.
• Understanding of solid mechanics and fluid dynamics principles.
• Develop and execute feasibility testing in support of product development.
• Create technical drawings, reports, data and other documents.
• Perform risk analysis, FMEA etc.
• Collect, calculate and interpret data from experiments
• Review, observe, and document Human Factors testing activities including but not limited to Formative and Summative testing
• Ensure that every product is robust in design; perform engineering analysis and routinely provide evidence of robustness, reliability and efficacy.
• Perform product and process root cause analysis and problem solving
• Fundamental understanding of statistics
• Design, development, verification and validation of combination products in support of Teva’s global R&D pipeline with special focus on delivery of biologics
• Occasional travel to locations where activity is current

Qualifications

Required:

M.S. Mechanical or Biomedical Engineering

Function

Sub Function

Reports To

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