Joana Rosado
About Joana Rosado
Joana Rosado is a Senior Quality Manager and Technical Director at Bristol Myers Squibb in Portugal, with over a decade of experience in regulatory affairs and pharmacovigilance.
Current Role at Bristol Myers Squibb
Joana Rosado is currently serving as the Senior Quality Manager and Technical Director at Bristol Myers Squibb in Portugal. Her role focuses on ensuring the highest standards of quality management within the organization. She employs her extensive experience in regulatory affairs and quality assurance to oversee various technical operations and compliance protocols.
Previous Experience at Celgene
Prior to her current role, Joana Rosado worked at Celgene from 2018 to 2020 as the Regulatory Affairs and Quality Manager, Technical Director in Lisbon, Portugal. During her tenure, she played a significant role in regulatory compliance and quality management just before the acquisition of Celgene by Bristol Myers Squibb.
Tenure at Amgen
From 2015 to 2018, Joana Rosado was employed at Amgen as Technical Director, Regulatory Affairs Manager, and Local Qualified Person for Pharmacovigilance in the Lisbon area, Portugal. Her responsibilities included ensuring regulatory compliance and overseeing pharmacovigilance activities, further solidifying her expertise in these domains.
Academic Background
Joana Rosado has a robust academic background in pharmaceutical sciences and health economics. She achieved an Integrated Master in Pharmaceutical Sciences from the Universidade de Coimbra, from 2002 to 2008. Additionally, she studied Applied Health Economics at the Escola Nacional de Saúde Pública, Universidade Nova de Lisboa. Furthermore, she obtained expertise in Integrated Systems: Quality, Environment, Safety, and Social Responsibility from SGS Portugal, from 2010 to 2012.
Experience at Jaba Recordati and Earlier Roles
Joana Rosado's early career includes significant roles at Jaba Recordati, where she served as Regulatory Affairs Manager and Local Back-up of QPPV for Pharmacovigilance from 2011 to 2015 in Porto Salvo. She also gained valuable experience at Ortho Clinical Diagnostics and Pharsolution, taking on various roles related to quality assurance, regulatory affairs, and pharmacovigilance. Her diverse background spans multinational pharmaceutical companies and specialized consulting firms.