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Nabídka volných pracovních míst

With 530 years of heritage, more than 3.000 employees, a leading Research and Development Center and two major production sites in Prague and Bucharest, Zentiva strives to be the champion of Generics to support the daily healthcare needs of people living in Europe.The growth of our organization brings new opportunities for our people to fulfil their potential. It also positions us well to attract the best talent and retain our team to secure our success for future generations. Join us!

Regulatory Data Adminstrator (DPČ)

Your responsibilities:

To support registration processes related to the preparation of registration documentation for all types of submissions and data management in data management systems and databases of Regulatory Affairs department


  • Registration data entry and actualization in databases of registered portfolio
  • Gaining and control of registration and pharmacovigilance data needed for submissions for EMA
  • Verification of compliance of internal documentation and approved registration documentation
  • Reports controlling
  • Controlling of obtained Decisions of registration agencies and its entra into documentation system

We require:

Secondary school / University Degree in Chemistry, Pharmacy, Natutal Science is advantage

  • Experience in Regulatory Affairs is advantage
  • Very good PC skills
  • English (Upper Intermediate)
  • Focus on detail, accuracy

We offer:

  • Challenging career opportunity to work for a successful international company
  • Opportunity to broaden your knowledge and expertise in your field


Klára Pavlíková