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Regulatory affairs specialist (m/f)
O poslu
Regulatory affairs specialist responsible for chemical, pharmaceutical and biological documentation/medicinal products quality (m/f) - Zagreb
Respecting the provisions of the Medicinal Products Act, your main responsibility will be to participate in the preparation of all documents required for obtaining new and retaining existing marketing authorizations for placing medicinal products on the market.
O zaposleniku
• University degree from the Faculty of Pharmacy and Biochemistry (Degree in Pharmacy) or the Faculty of Chemical Engineering and Technology, the Faculty of Science (Chemistry Studies) and Faculty of Food Technology and Biotechnology
• At least 1 year of professional work experience in medicinal products registration (the quality of the medicinal product)
• Developed organizational and communication skills with a strong sense of teamwork
• Persistent and systematic, resourceful, energetic and willing to overcome obstacles in order to achieve envisaged business objectives
• Excellent knowledge of English both - spoken and written
In addition to the aforementioned requirements, capabilities and characteristics, eligible candidates are expected to have very good computer skills and a valid driving license – category B.
The company will provide you with:
• Very good income
• Motivating work environment (company regularly invests in the development of employees’ professional competences)
• Professionally challenging work in a dynamic team environment
If you believe that you meet the stated expectations and are willing to accept the offered business challenge, please send your motivation letter and CV by 15 September 2014 to the following email:
[email protected] , listing reference number 02.111 in the subject line.