• Maintained and updated MMR, Batch Records, document control system, product specifications and all other documents to ensure compliance with all regulations and internal standards. • Reviewed cGMP related policies and SOPs and conducted internal inspections to meet FDA requirements• Reviewed and released product batch records for raw materials, labels, packaging materials and finished products• Supported Quality Specialists to research structure and function claims for dietary supplement products• Conducted inspections and released raw materials, components, in process and finished materials after appropriate quality inspection is performed

• Served on a 5-person team of NYU Wagner Graduate Candidates to design a growth strategy plan for the Institute for Innovation in Medical Education at NYU to gain future funding• Evaluate current programs with the Executive Director & senior leadership and provide critical review for improvements and areas of growth• Conduct environmental scan, literature review, market research, staff interviews, and proposed implementation timeline

• Investigated USP, BP, CP and drug registration regulations for drug exportation. • Translated Quality Assurance and Quality Control documents to English for each registration drug• Completed and submitted all registration documentations to foreign drug authorities• Hosted GMP audits by foreign drug authorities for the targeted registrations

Participated in the research of the functional study of PTPA (PP2A Phosphatase Activator)

Coordinated in the research of creating synthetic materials capable of delivering multiple types of drugs within a single payload