Bibi Ayesha Shariff

I’m a results-driven Pharmacist with experience across Quality Assurance, Regulatory Affairs, Clinical Research, Hospital Pharmacy, and Community Pharmacy environments. I focus on batch release and ensuring GMP/GxP compliance by reviewing Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and analytical documentation before release.

In my QA and QA/RA roles, I’ve supported deviation, CAPA, change control, incident reporting, internal audits, stability programs, and product complaint investigations—always strengthening QMS documentation and regulatory submissions. I also bring clinical research support under GCP guidelines, investigational product management support, and pharmacovigilance expertise to help protect patient safety and maintain high pharmaceutical quality standards.