Shirel Méndez
About Shirel Méndez
Shirel Méndez is a Regulatory Affairs Specialist at Bristol Myers Squibb with experience in regulatory roles at Eurofarma and a background in Biological Pharmaceutical Chemistry from Universidad Nacional Autónoma de México.
Title
Shirel Méndez is currently serving as a Regulatory Affairs Specialist at Bristol Myers Squibb.
Professional Experience at Bristol Myers Squibb
Shirel Méndez has accumulated extensive experience at Bristol Myers Squibb, serving in various regulatory roles. She is currently a Regulatory Affairs Specialist. Prior to this, she worked as a Regulatory Affairs Analyst from 2020 to 2021 for 5 months. She also held the position of Regulatory Affairs Intern from 2019 to 2020 for 1 year.
Experience at Eurofarma
Shirel Méndez held the position of Regulatory Affairs Analyst at Eurofarma from 2021 to 2022 for 9 months. During this time, she contributed to regulatory matters within the company.
Educational Background
Shirel Méndez studied at Universidad Nacional Autónoma de México (UNAM), where she pursued a degree in Biological Pharmaceutical Chemistry. She completed her thesis and is in the process of obtaining her professional degree. Her educational tenure spanned from 2015 to 2019.
Research and Development Experience
In addition to her regulatory roles, Shirel Méndez gained practical experience during her Professional Practices and Thesis Project at the Instituto de Investigaciones Biomédicas, UNAM from 2019 to 2020 for 1 year. She has hands-on experience in the development and evaluation of a DNA vaccine.