Carlton National Resources
Ryan Prifti has a strong background in technical recruitment, starting with their role as an Account Manager at Oxford International in 2004. From 2008 to 2009, they worked as a Senior Technical Recruiter at Experts Technical Staffing. Ryan then moved on to Black Diamond Networks, where they served as a Senior Technical Recruiter from 2010 to 2014. At IntePros Consulting, they took on the role of Branch Manager from 2014 to 2018, overseeing the Quality/Regulatory Compliance group. Currently, they are working at Carlton National Resources as the Managing Director, starting in August 2022.
Ryan Prifti obtained a Bachelor of Arts degree in Criminal Justice from Curry College. Ryan also attended Archbishop Williams from 1992 to 1996, but there is no information regarding any degrees or fields of study during this time. Additionally, Ryan Prifti attended Manomet Elementary, but no details regarding degrees or fields of study at this institution are provided.
This person is not in any offices
Carlton National Resources
2 followers
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.