
Analytical Chemistry professional with over 6.5 years of experience in pharmaceutical Quality Control, method validation, stability studies, and R&D support. Skilled in HPLC, GC, UV-Vis, and a wide range of analytical techniques. Adept at maintaining regulatory compliance (ICH, WHO, ALCOA+), managing data integrity, and producing clear scientific documentation. Proven ability to work in cGMP environments with cross-functional teams and resolve analytical challenges efficiently.