Vinicius Izidio Almeida
About Vinicius Izidio Almeida
Vinicius Izidio Almeida is a Senior Regulatory Analyst at Bristol Myers Squibb in São Paulo, Brazil, with extensive experience in regulatory affairs across several multinational pharmaceutical companies.
Professional Title and Current Role
Vinicius Izidio Almeida is a Senior Regulatory Analyst currently employed at Bristol Myers Squibb. Based in São Paulo, Brazil, he has been with the company since August 2020. His role leverages his extensive experience in regulatory affairs within the pharmaceutical industry.
Previous Work Experience
Vinicius Izidio Almeida has accrued a substantial amount of experience in regulatory affairs. Before his current role, he spent two years at AstraZeneca as a Regulatory Affairs Analyst (2018-2020) and two years as a Jr Regulatory Affairs Analyst (2016-2018) in Cotia, São Paulo. He also worked at Pfizer as a Jr Regulatory Affairs Analyst from 2015 to 2016 for 10 months and at AbbVie as a Regulatory Affairs Intern from 2014 to 2015. Additionally, Almeida has consulted for Farma Júnior Consultoria from 2008 to 2011.
Educational Background
Vinicius Izidio Almeida studied at the University of Manitoba, focusing on Health General Science and participating in the Science without Borders program for one year from 2012 to 2013. He also holds a Bachelor's degree in Pharmacy from USP, completed over seven years from 2008 to 2015.
Leadership and Management Roles
Apart from his regulatory roles, Vinicius Izidio Almeida has held leadership and project management positions. He was the Diretor Presidente at Núcleo USP Jr. - Núcleo das Empresas Juniores da USP for 11 months in 2011. He also interned in Project and Portfolio Management at Natura in 2012, where he gained experience in managing complex projects.
Diverse Professional Background
Vinicius Izidio Almeida's career showcases his versatility and adaptability, having worked in both multinational pharmaceutical companies and local consultancy firms. His diverse experience spans various facets of the pharmaceutical industry, particularly in regulatory affairs, project management, and consultancy.