Teva Device Engineer 

United States, Pennsylvania, East Bradford Township 

808210692

As a Development Engineer II you will work in the R&D organization and be responsible for managing the 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.

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

Minimum requirements:

• MS Mechanical Engineering or 1-3 years experience (Preferred)
• MS Biomedical Engineering or 1-3 years experience

Director Biopharmaceuticals Combination Products

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