Sina Akhavansalamat

Result-oriented Pharmaceutical Technical Manager with 10 years of experience in laboratory management, formulation development, and manufacturing operations. Proven expertise in establishing and auditing QA/QC systems in compliance with PIC/S, EU GMP, and ICH guidelines. Specialized in in-vitro dissolution studies, formulation optimization for solid dosage forms (tablets/capsules), and tech transfer. Adept at leading cross-functional teams of engineers to deliver high-quality analytical and production solutions.