Carlton National Resources
Steven Pelletier is an experienced Senior Technical Recruiter currently employed at Carlton National Resources since October 2022, specializing in the Life Sciences sector. Prior to this role, Steven served as a Recruiting Manager at Softworld, focusing on a wide range of consulting services within Life Sciences from October 2021 to October 2022. Between August 2017 and September 2021, Steven held the position of Recruiting Lead/Senior Technical Recruiter at Black Diamond Networks, concentrating on Clinical and Regulatory Affairs as well as various technical needs in the Pharmaceutical, Biotech, and Medical Device industries. Steven began a career in recruitment at Aerotek from June 2014 to August 2017 as an Account Recruiting Manager and Senior Technical Recruiter in Engineering. Steven holds a BS/BA degree in Marketing from Suffolk University's Sawyer Business School, obtained in May 2011.
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.