Talita Hernandez
About Talita Hernandez
Talita Hernandez is a Regulatory Affairs Analyst at Bristol Myers Squibb in São Paulo, Brazil, with extensive experience in regulatory affairs across multiple pharmaceutical companies.
Current Position at Bristol Myers Squibb
Talita Hernandez is currently working as a Regulatory Affairs Analyst at Bristol Myers Squibb in São Paulo, Brasil. Her role involves ensuring that the company complies with all the regulations and laws pertaining to the pharmaceutical industry. She is part of a team that helps to secure regulatory approval for new products and maintains compliance for existing products.
Previous Experience at Baxter International Inc.
From 2018 to 2021, Talita Hernandez worked at Baxter International Inc. as a Regulatory Affairs Analyst in São Paulo e Região, Brasil. During her three-year tenure, she was responsible for managing regulatory submissions, ensuring continuous compliance with regulatory standards, and supporting product registration and market expansion efforts.
Experience at Mundipharma
Between 2015 and 2018, Talita served as a Regulatory Affairs Analyst Latam at Mundipharma in São Paulo. Over three years, she handled regulatory affairs for the Latin American region, coordinating submissions and managing regulatory requirements across multiple jurisdictions.
Early Career and Education
Talita Hernandez began her career in 2007 at Ranbaxy Farmaceutica Ltda as a Representante/Propagandista, where she worked for two years. She then transitioned into regulatory roles with increasing responsibility, eventually moving into the position of Analista de Apoio Científico at Shire Pharmaceuticals from 2011 to 2014. She studied at Centro Universitário das Faculdades Metropolitanas, achieving her Graduação from 2007 to 2012. Later, she pursued further education at ECM - European College of Management and Faculdades Oswaldo Cruz, where she completed a Pós Graduação from 2014 to 2015.
Comprehensive Background in Regulatory Affairs
Talita Hernandez has amassed extensive experience in the field of regulatory affairs, holding roles in multiple respected pharmaceutical companies. Her work history includes positions at CooperVision, Cristália Produtos Químicos Farmacêuticos Ltda, and a significant role as an Analista de Apoio Científico at Shire Pharmaceuticals. She has developed a profound understanding of regulatory practices, supporting drug approvals and maintaining compliance across varied markets.