Boston, Massachusetts, United States
I’m currently pursuing my Master’s degree with a focus on regulatory affairs. I’m fascinated by the intersection of science, policy, and how strong regulatory systems make innovation possible. As I begin my graduate journey, I’m building a solid foundation in regulatory frameworks, quality systems, and healthcare oversight. I’m especially interested in how emerging technologies can move from research to real world impact in a way that is both ethical and compliant. Always open to learning, connecting, and exploring opportunities within regulatory and healthcare innovation.
• Reviewed regulatory dossiers for compliance with national guidelines and global standards in medical devices and biopharmaceuticals. • Submitted dossiers to the Pharmaceutical and Poisons Board (PPB) and coordinated responses to regulatory queries. • Managed product sample cataloging for laboratory analysis and drafted official correspondence to support submissions.
Read and understood all SOPs and Bench Aids. Carried out Quality Control Tests daily to ensure all machines and reagents work properly. Tested patient samples within their microbiology, hematology, chemistry department, and RT-PCR tests in the Molecular Biology department. Conducted various tests in the pathology department using Sysmex XN- 330, Cobas Integra 400 plus, Cobas e411, Bio-Rad D-10 and Mini Vidas.
Read and understood all SOPs and Bench Aids. Carried out Quality Control Tests daily to ensure all machines and reagents work properly. Collaborated with the microbiology, hematology, and special chemistry department. Conducted various tests in the pathology department using Sysmex XN- 330, Cobas Integra 400 plus, Cobas e411, Bio-Rad D-10 and Mini Vidas.