Carlton National Resources
Justin G. is a seasoned professional with a diverse background in technical recruitment and program operations management. Currently serving as a Technical Recruiter at Carlton National Resources since February 2022, Justin previously held the role of Assistant Program Operations Manager at People Incorporated from December 2020 to August 2021. Prior experience includes a significant tenure as a Senior Direct Care Provider at Cooperative Productions, which lasted from September 2011 to January 2020. Justin's foundational skills were developed in the United States Air Force, where responsibilities as an Aircraft Avionics Specialist from July 2001 to June 2007 included installing, maintaining, and troubleshooting avionics systems in military aircraft. Academically, Justin holds a Bachelor’s Degree from Bridgewater State University, graduating Cum Laude with a 3.5 GPA, and was active in the Economics Club as well as Accounting and Finance.
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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.