Adriana Calinescu is an experienced regulatory affairs professional with over two decades in the field. Currently serving as a Senior Regulatory Affairs Specialist at Zentiva since September 2018, Adriana has previously held similar roles at Sanofi from September 2009 to August 2018 and at Zentiva, Sicomed S.A. from March 2005 to September 2009. Adriana began the career as a Junior Regulatory Affairs Specialist at EUROPHARM – GlaxoSmithKline S.R.L. from November 1998 to March 2005. Adriana holds a Diploma of Chemical Engineer with a Biochemistry Licence, completed at Lucian Blaga University in Sibiu between October 1991 and June 1996.
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Zentiva
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Zentiva is a Pan-European Platform developing, manufacturing and providing high-quality and affordable medicines to more than 100 million people in Europe. Zentiva has 4 wholly owned manufacturing sites and a broad network of external manufacturing partners to ensure supply security. We offer solutions in key therapeutical areas like Cardiology & Circulation, Diabetes, Oncology, Respiratory, CNS and focus on expanding our portfolio in self-care. The company is Private Equity owned, delivering sustainable double-digit growth, with an ambitious 5-year plan for further strong (organic and inorganic) growth across Europe. We are a team of almost 5,000 unique talents bonded together by our mission to deliver high-quality and affordable medicines to people who depend on them every day. We want Zentiva to be a great place to work, where everyone feels welcomed and appreciated and can be their true selves contributing to the best of their ability.