Internship Farmacovigilenta

Scurta descriere a companiei

Zentiva Group, one of the most important generic drug manufacturers in Europe, owns in Romania the companies Zentiva Romania, Solacium Pharma, Labormed factory and Labormed Pharma Trading.

Through the two factories in Bucharest (Zentiva factory and Labormed-Alvogen factory), Zentiva has consolidated its impact and contribution in the local pharmaceutical market, becoming the largest drug manufacturer on the market.

Zentiva in Romania is also the leader in volumes of the total medicine market and leader in volumes and value in the generic medicine market. 1 out of 4 medicines sold in pharmacies is a Zentiva medicine.

The Zentiva factory has been operating uninterruptedly since its inauguration in 1962 and the Labormed factory is one of the most modern units for the production of solid oral medicines in Romania, the result of the first greenfield investment in the pharmaceutical industry in our country.

In Romania, the Zentiva team brings together over 1300 employees, of which 870 are involved in industrial production activities, 350 are employed in commercial activities and approximately 100 people in global positions

For the care of our team and for the good practices of human resources, Zentiva Romania was recognized as Top Employer 2022 by the organization Top Employer Institute.

Cerinte

• Educaţie: studii universitare în farmacie, medicina, biologie;
• Caracteristici: rigurozitate, lucru în echipă, viziune în perspectivă;
• Integritate, tenacitate şi adaptabilitate în situaţii complexe şi deseori medii în schimbare;
• Abilităţi bune de comunicare, adaptabilitate şi sensibilitate interculturală;
• Cunostinte operare computer, in special MS Word, Excel;
• Capacitatea de a livra performanţe înalte atât individual cât şi în echipă;
• Nivel mediu de limba engleza.

Responsabilitati

• Activitati de back-up in farmacovigilenta,
• Ajuta la pregatirea dosarelor pentru aprobarea masurilor aditionale de minimizare a riscului ce trebuie trimise spre aprobare autoritatilor competente,
• Verifica informatiile primite (la anumite molecule) in rapoartele de monitorizare a presei referitoare la evenimente de farmacovigilenta,
• Ajuta la pregatirea dosarelor de aprobare a preturilor la medicamentele de uz uman.