Adriana Gutierrez is an experienced regulatory affairs professional with over 30 years of expertise in the pharmaceutical and healthcare sectors. Currently serving as Regulatory Affairs Manager at Key Pharmaceuticals since June 2019, Adriana is responsible for understanding and assessing the impact of regulatory changes, managing product registrations, ensuring compliance, and providing support to overseas companies. Prior to this role, Adriana worked at Pfizer as a Regulatory Manager from November 2001 to April 2019, where responsibilities included developing registration strategies, maintaining compliance for existing products, and improving regulatory systems. Earlier experience includes positions at Faulding Pharmaceuticals, Cenovis, and a role as a Quality Analyst, where Adriana gained extensive knowledge in product registration and regulatory compliance across various international markets. Adriana holds a Bachelor's degree in Biochemistry from the University of Buenos Aires.
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