Hilaria Amuzu
About Hilaria Amuzu
Hilaria Amuzu is a Regulatory Affairs Specialist at Bristol Myers Squibb in Australia, with a background in global regulatory submissions and compliance for pharmaceutical products.
Title
Hilaria Amuzu is currently working at Bristol Myers Squibb as a Regulatory Affairs Specialist in Australia. She has extensive experience in regulatory affairs within the pharmaceutical industry.
Education and Expertise
Hilaria Amuzu has a comprehensive educational background in both biological sciences and regulatory affairs. She earned her Bachelor’s Degree in Animal Biology/Zoology from the University of Ghana from 2000 to 2004. She followed this with a Master’s Degree in Medical Entomology from the same institution between 2006 and 2008. She then completed her Doctor of Philosophy (Ph.D.) in Biological Sciences at Monash University from 2012 to 2016. Additionally, she has a Regulatory Affairs Certificate: Pharmaceuticals from the Regulatory Affairs Professionals Society (RAPS) University, achieved in 2020 over an 11-month period.
Professional Background
Hilaria's career encompasses various roles in research and regulatory affairs. From 2004 to 2010, she worked as a Principal Research Assistant at the Noguchi Memorial Institute for Medical Research (NMIMR) in Ghana. In 2017, she briefly served as a Research Officer at Monash University in Clayton, Victoria, Australia. From 2017 to 2021, Hilaria was a Global Pathogen Safety Scientist at CSL Behring in Broadmeadows, Victoria, Australia. Her current role is as a Regulatory Affairs Specialist with Bristol Myers Squibb in Australia.
Achievements in Regulatory Affairs
At Bristol Myers Squibb, Hilaria has contributed to the development of regulatory strategies for new pharmaceutical products. She has demonstrated expertise in global regulatory submissions and compliance, and has participated in cross-functional teams to ensure regulatory requirements are met for product launches. She has also conducted regulatory risk assessments and provided strategic guidance to project teams. Additionally, Hilaria has experience liaising with regulatory authorities to facilitate product approvals and maintain compliance.