Renee McNeil Porter has extensive experience in quality assurance and compliance within the biotechnology and pharmaceutical sectors. Currently serving as a QA Contractor/Consultant at Meridian BioGroup since October 2008, Renee previously held the position of Director of Quality Assurance at NantOmics, LLC from November 2015 to May 2018, leading the establishment of a quality department for a diagnostic company focused on personalized cancer treatment. Other notable roles include Director of Quality at KPL, Senior Compliance Specialist at Phoenix Imperative, QA/QC Manager at Johns Hopkins University, and various positions in quality assurance and technical specialties at Cambrex BioScience, Osiris Therapeutics, Cel-Sci Corp, and SITEK Research Labs. Renee holds a B.S. in Marine Science/Biology from the University of Miami, completed in 1994.
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