Tamika Cathey

Tamika Cathey is a seasoned professional in the regulatory and quality compliance sector, currently serving as Principal Program Lead Pharma Biotech at NSF since August 2023, where responsibilities include developing proposals for large projects and managing project delivery. With extensive experience as a Senior Regulatory Scientific Advisor at TDC & Associates Consulting from April 2012 to September 2023, Tamika provided consulting across pharmaceutical and biotechnology sectors, focusing on quality system design and remediation plans for FDA enforcement. Additional roles include Managing Quality and Regulatory Consultant at Oriel STAT A MATRIX and Independent Consultant at EAS Consulting Group, LLC, where engagements involved executing mock FDA audits and delivering regulatory compliance training. Education includes a Bachelor's degree in Biology from Greensboro College, earned in 1999.