Carlton National Resources
Jack Mcwhirter is an experienced professional with a diverse background in business development, quality assurance, and project management. Currently serving as a Business Development Manager at Carlton National Resources since June 2023, Jack specializes in hardware and software engineering, with competencies in software embedded engineering, firmware, and RF design. Prior to this role, Jack held various positions at ALKU, where responsibilities included managing life science contracts focused on pharmaceutical regulatory compliance from January 2022 to May 2023. Jack also gained valuable leadership experience as a Branch Manager for Young Entrepreneurs Across America and as a Project Manager for Student Painters, achieving significant revenue growth and effective project execution. Jack earned a Bachelor of Business Administration in Management and Marketing from the Manning School of Business, UMass Lowell, in 2022.
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.