Galia D.

Over 20 years of diverse experience in the biotech and pharmaceutical industry, including 18 years in analytical chemistry and over 5 years in QA leadership. Strong background working with regulatory compliancy authorities: FDA, MOH (GMP), and the ISRAC (GLP&GCLP). Expert in auditing validation protocols and validation reports. Specialized in writing SOPs, managing Deviation Reports, Change Controls, CAPAs, and Risk Assessments. Experienced in auditing sub-contractor laboratories to ensure