Patrick Snowhill

Background

About Patrick Snowhill

Excellent R&D/Product Development scientist and lecturer. I have worked in both the academic and commercial setting. I have authored several papers, given podium presentations, and taught at the graduate and undergraduate level. I have developed several commercial products and assisted Regulatory Affairs in writing many FDA and OUS applications to support regulatory filings. I have also assisted manufacturing in trouble shooting process issues and developed both process and method validations. I am versed in GLP and GMP and have worked on several teams to develop and run IOQ/PQ validations as well as design verifications. I am used to working in a regulated industry under the auspices of 21 CFR Part 820 (QSR) and ISO 13485. I have also provided technical support and documentation for Clinical Affairs in complaint investigations. However, I am equally comfortable working in a purely research oriented facility. I am also experienced in working with and speaking to physicians. As a (principal) scientist in the medical device industry I have provided assistance to and/or taken the lead on Quality, Regulatory, Manufacturing, Marketing, Clinical, Project Management, as well as Product Development needs. I feel I am an excellent problem solver and have a broad area of expertise. Specialties: Medical device development, endovascular devices, GLP, GMP, QA, RA, DFSS, biocompatibility (ISO 10993), pre-clinical studies, histology, statistical analysis, ISO 14971, skilled analytical thinker, excellent practical laboratory skills, good at mastering analytical equipment operation and theory, excellent situational awareness, understand the big picture, good business sense.