Linnea Gustén

Linnea Gustén

Senior Regulatory Manager Nordics And Distributor Markets @ Bristol Myers Squibb

About Linnea Gustén

Linnea Gustén is the Senior Regulatory Manager Nordics and Distributor Markets at Bristol Myers Squibb, with over a decade of experience in pharmacovigilance and regulatory affairs.

Current Role at Bristol Myers Squibb

Linnea Gustén is currently serving as the Senior Regulatory Manager Nordics and Distributor Markets at Bristol Myers Squibb. In this role, she oversees regulatory activities and ensures compliance with regional and local regulations for the Nordic countries and distributor markets. She brings extensive experience in regulatory affairs and pharmacovigilance to this position.

Career Path at Bristol Myers Squibb

Linnea Gustén has been with Bristol Myers Squibb for over four years, during which she has held multiple positions. She began as a Senior Pharmacovigilance Associate in 2017, where she worked for three years in Solna, Stockholms län. In 2019, she transitioned to the role of Regulatory Manager, a position she held for one year. She has since advanced to her current role as Senior Regulatory Manager Nordics and Distributor Markets.

Previous Positions in Pharmacovigilance and Drug Safety

Before joining Bristol Myers Squibb, Linnea Gustén gained substantial experience in pharmacovigilance and drug safety. She worked as a Pharmacovigilance Manager at Meda from 2015 to 2017 and as a Drug Safety Associate at McNeil Consumer Healthcare from 2012 to 2015. Earlier in her career, she served as an Assistant at the Medical Products Agency in Uppsala and as a Data Entry specialist for her Master thesis project at Smerud Medical Research.

Educational Background in Biomedicine

Linnea Gustén pursued her education at Uppsala University, where she completed a Master's degree in Biomedicine from 2006 to 2011. Prior to this, she attended Stockholms musikgymnasium, completing a three-year program in Naturvetenskap, which laid the foundation for her scientific and regulatory career.

Extensive Experience in Regulatory Affairs and Pharmacovigilance

With over a decade of experience in the pharmaceutical industry, Linnea Gustén has amassed significant expertise in both regulatory affairs and pharmacovigilance. Her career spans various roles, from Data Entry and Assistant positions to senior managerial responsibilities in regulatory and pharmacovigilance capacities. She has worked in both the public and private sectors, including at the Medical Products Agency and multiple pharmaceutical companies.

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