Gergana Krasteva

Gergana Krasteva is an experienced professional with 15 years of experience in the pharmaceutical, biotech, and medical devices industry. She has a strong background in validation, GMP, GLP, SOP, and Capa. Gergana has worked in various roles, including Senior Scientist and Project Manager at Roche in Switzerland and Senior QC Scientist and Supervisor at Genpharm Inc. in Canada. She is skilled in analytical method development, process characterization, and validation. Gergana is proficient in reviewing data, documentation, and preparing documents for FDA submission. She has international industry experience from Europe, Canada, and the USA.