Licensed Pharmacist with experience in pharmacovigilance, pharmaceutical quality assurance, and regulatory compliance. I currently work as a Pharmacovigilance Associate, where I process and review safety cases, ensure data quality, and support compliance with global pharmacovigilance regulations while consistently meeting strict deadlines.
Prior to this, I worked in pharmaceutical manufacturing as a Quality Assurance and Compliance Officer, managing SOPs, supporting FDA regulatory requirements, conducting document reviews, handling CAPAs and complaints, and participating in internal and external audits. These experiences strengthened my attention to detail, analytical thinking, and ability to work accurately in highly regulated environments.
I am proficient in documentation, data entry, Microsoft Office (Excel, Word, and PowerPoint), technical writing, research, and cross-functional collaboration. I am a fast learner, highly organized, dependable, and comfortable working independently in a remote environment.
I am seeking long-term remote opportunities where I can contribute my expertise in pharmacovigilance, regulatory affairs, medical and scientific writing, clinical research support, quality assurance, data management, or administrative operations. I am committed to delivering accurate, high-quality work while maintaining professionalism, confidentiality, and reliability.
