
I am a pharmaceutical professional with experience in GMP-regulated environments and a strong focus on patient safety. My work in aseptic manufacturing has developed my attention to detail, accuracy in documentation, and ability to follow strict regulatory standards. With academic exposure to clinical trials and ICH-GCP, I have a good understanding of drug safety principles. I am now looking to transition into pharmacovigilance, where I can apply my skills in data accuracy and regulatory compliance to support effective safety monitoring.