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Paul Wood

Validation /quality Engineer at Carlton National Resources

Paul Wood is an experienced engineering professional with a focus on validation and quality assurance. Currently serving as a Validation/Quality Engineer at Carlton National Resources since November 2020, Paul is involved in validations, remediation of quality documents, and project management for the EUMDR project. Previous roles include Validation Engineer at Cloud Staffing Professionals, Project Engineer at Clarke Solutions, and Sr. Validation Engineer at CoorsTek Medical LLC. Paul has also held engineering positions at Thermo Fisher Scientific, Allegiant International, Cooper Standard Automotive, and DePuy Orthopaedics, where responsibilities spanned project management, process improvements, and equipment validations. Paul holds a Bachelor of Science degree from Purdue University, obtained between 1982 and 1986.

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Fairborn, 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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