RH

Rick Holbrook

Rick Holbrook is an experienced RF Engineer with a comprehensive background in the field, holding various positions since 2005. Current engagement includes working for multiple companies as an RF Engineer since 2019. Previous roles include RF Engineer at General Dynamics Mission Systems from 2018 to 2019, RF Systems Engineer and RF Applications/Reference Design Engineer at RFMD (now Qorvo, Inc.) from 2013 to 2018, and RF Engineer at Nest Labs from 2012 to 2013. Additional experience encompasses positions at RFMD, ON Semiconductor, SMSC, and Motorola, where Rick Holbrook developed a strong foundation in technical marketing, applications engineering, and design engineering. Rick Holbrook holds a BS and MS in Electrical Engineering from California State University, Fullerton, and has partial completion of a PhD in Electrical Engineering from Ohio University.

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Phoenix, United States

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Carlton National Resources

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Carlton National Resources is a national staffing firm focused on temporary, individual contract placement of senior level Hardware and Software Engineers and Life Science Professionals. We work across a broad range of industries. Our technical core competencies include Software Embedded Engineering, Software Applications Development, Firmware/DSP, Hardware, FPGA/ASIC Design and Verification, RF Design amongst others. At Carlton we also specialize in placing temporary, individual or team based consultants in the Medical Device and Pharmaceutical Industries. Quality management is a multidimensional issue covering more than just verification that a finished product meets certain expectations. As a component of regulatory standards, quality management requires a system for controlling, monitoring, and verifying any activity or process that could affect product conformance. Regulatory compliance requirements extend throughout the full product lifecycle from development through approval, manufacturing, launch, and required post market reporting. Whether manufacturing medical devices or launching new pharmaceuticals, meeting global compliance requirements starts from the first specification draft.


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51-200

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