Senior Mechanical Engineer, R&D

4 weeks ago


Los Angeles, United States Analog Group Inc Full time

The individual will contribute in the development of existing and new medical technologies and applications. Duties and Responsibilities:

· Define and guide development ofelegant mechanical designs that meet requirements for product performance,cost, reliability, and manufacturability. · Develop designs for all phasesof product development from proof-of-concept through manufacturing. · Drive design verification by testing design performance in the lab and design validation by developing fast-turn clinical prototypes for use in the research clinic. · Contribute regularly totechnical design reviews, project scheduling, and development of new productconcepts and applications. · Use FEA simulation tools tomodel mechanical assemblies and guide design development. · Other duties as assigned. Position Requirements:

· B.S. in Mechanical engineeringwith 5+ years related mechanical design experience for capital equipment,laser, or medical devices. Graduate degree a plus. · Experienced in design of opto-mechanicalassemblies. Experience designing mechanical actuation assemblies such as laserbeam scanning systems, translation and rotation stages is a plus. Knowledge ofstrain-free mounting techniques for optics using adhesives is a plus. · Strong understanding ofGD&T principles and ability to evaluate and apply them to precisionmechanical designs. · Proven 10+ years of CAD designexperience. SolidWorks preferred. · Extensive knowledge of leadingmanufacturing technologies including plastic injection molding, sheet metalmanufacturing, and high precision machining. · Proven communication skills andability to make design recommendations based on cross-functional inputs(Engineering, Clinical, Manufacturing, Quality, and Regulatory). · Ability to apply FEA simulationtools to develop designs by correlating simulation results with empirical testdata. · Basic working knowledge,electronics, optics, and numerical data analysis (Excel, Matlab, orequivalent). Data acquisition skills such as LabView is a plus. · Familiarity with FDA QualitySystems Regulations/Design Control requirements and their application toprojects from design inception to manufacturing release. · Knowledge and experience withIEC 60601 compliance standards and ISO14971 Risk Management requirements andtechniques.

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