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Nabídka volných pracovních míst


With 530 years of heritage, more than 2,500 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!

PV Risk Management Expert

Your responsibilities:

  • Participation in routine Pharmacovigilance activities
  • Planning, development and maintenance of Risk Management Plan documents
  • Providing expertise in pre- and post-marketing risk management of Zentiva portfolio
  • Clear and effective communication and cooperation with relevant stakeholders
  • Providing appropriate product risk minimization strategy for ensuring patient safety in light of benefit/risk assessment in coordination with relevant functions (pharmacovigilance, medical, labeling, regulatory, local functions), interacting with health authorities

We require:

  • University degree (medical or pharmacy)
  • Previous experience in pharmacovigilance, clinical or regulatory practice is advantageous
  • Proven excellent communication and organization skills
  • Interest in the area of pharmacovigilance
  • Willingness and desire to learn new things
  • Advanced level of English
  • Strong PC skills
  • Detail oriented, hardworking personality
  • Team player

We offer:

  • An opportunity to work for in an international environment
  • An opportunity to broaden your knowledge and expertise in the field of drug safety
  • Work in friendly environment
  • Continuous personal development
  • An attractive compensation & benefits package

Contact

Zentiva
Enikö Gálik