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.
Your experience and qualifications
MS Mechanical Engineering or 5-7 years experience (Preferred)
BS Mechanical Engineering or 7-10 years experience
MS Biomedical Engineering or 5-7 years experience
BS Biomedical Engineering or 7-10 years experience
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