Mahvash Suhail

I’m a detail-oriented M.Pharm graduate specializing in Pharmaceutical Analysis, with experience in analytical method development, regulatory documentation, and pharmacovigilance support. I focus on compliant, data-integrity-first work aligned with ICH and GLP guidelines.

As an Officer at Scott Edil Pharmacia, I conducted analytical method development and validation as per ICH guidelines. I also supported regulatory documentation and dossier preparation, maintained GLP compliance, and ensured data integrity in laboratory operations while supporting quality control testing and pharmaceutical analysis processes.

During my internship at Sun Pharmaceuticals Ltd, I gained exposure to pharmaceutical manufacturing, quality systems, and regulatory compliance. I assisted in adverse drug reaction (ADR) reporting and pharmacovigilance documentation, working with cross-functional teams to ensure SOP adherence and timely documentation.

I build strong regulatory-ready documentation and validated analytical methods—covering CTD/eCTD documentation, dossier preparation & submission support, and RP-HPLC method validation. I’m now seeking opportunities in Drug Regulatory Affairs, Pharmacovigilance, Quality Assurance, and Pharmaceutical Research.