
I am enthusiastic pharmaceutical professional, passionate about Pharmacovigilance and Quality Assurance role with sound experience in pharmaceutical documentation, market complaint investigation, biomedical literature review, drug safety evaluation, and regulatory compliance. Good hand on analyzing adverse event data, ensure quality reporting, and support global pharmaceutical operations. Good knowledge about medical writing, ICH-GCP guidelines, and quality assurance systems. Seeking to contribute role in pharmaceutical company, pharmacovigilance, public health, or clinical research work.
Pharmacovigilance & Drug Safety
Adverse Event Reporting (SAE)
Biomedical Literature Review
Regulatory Compliance (ICH-GCP)
Quality Assurance
GMP Compliance
Documentation & Audit Readiness
Quality Control & Investigation
Technical Skills