
Quality Control Professional with about 5 years of progressive experience in the pharmaceutical industry, specializing in HPLC analysis, data integrity (ALCOA) and cGMP compliance. Proficient in cGMP, GxP, and QMS practices with proven ability to manage OOS/OOT investigations, CAPA, and data integrity (ALCOA+) requirements. Demonstrated expertise in operating and calibrating instruments such as HPLC, UV, FTIR, and KF Auto-titrator to ensure precise analytical outcomes. Recognized for maintaining audit readiness, mentoring team members, and consistently driving improvements in product quality and laboratory efficiency.
Certificate in Pharmaceutical Quality Assurance & Drug Regulatory Affairs