Medical Device and Regulation: Irvine CA at Irvine, Kentucky, USA |
Email: [email protected] |
From: Chandra N, Siri Info [email protected] Reply to: [email protected] Role name:EngineerRole Description:Project Planning and Execution, CAD, DMAIC, Change ManagementCompetencies:EIS : Medical Device & RegulationsExperience (Years):4-6Essential Skills:Bachelors degree in engineering or science (Biomedical, Mechanical, Electrical, Biology, etc)3+ years of medical device industry experience in design control and/or project engineeringDesirable Skills: Experience in New Product Development (NPD) with CAD software such as AutoCad or Solidworks is required. Strong knowledge on GD&T (Geometric Dimensioning &Tolerancing) Knowledge and experience in product development processes and design control is preferred. Experience with statistical analysis and design of experiments (DOE) preferred. In-depth knowledge of design of medical devices (neurovascular) preferred. Ability to quickly build connections with internal and external partners Ability to manage multiple projects and tasks simultaneously. Ability to read engineering drawings, GD&T, terminology, schematics Knowledge and experience in product development processes and design control is preferred. In-depth knowledge of design of medical devices preferred. Excellent verbal and written communication skills, including but not limited to, the ability to relate technical requirements, listen effectively, influence decision-makers by data and be able to receive constructive input from others. Ability to solve complex problemsCountry:United StatesBranch | City | Location:TCS - Los Angeles IRVINE Irvine, CA Keywords: California Medical Device and Regulation: Irvine CA [email protected] |
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Mon Jul 22 20:44:00 UTC 2024 |