At Zentiva, we are a team of 5.400 unique talents bonded together by our common mission. We believe our diversity is a source of great energy and strength, and we create a work culture and ethics where everyone feels appreciated, can be their true selves, and contribute to the best of their ability. Seeking for a balanced team across the company we welcome applications from all qualified candidates with various educational and industry experiences, cultural or ethical backgrounds, and different life experiences or abilities, regardless of their religious or philosophical beliefs or whomever they choose to love.
To compile, check and update registration documentation according to legislative requirements.
Coordination: to co-operate with appropriate departments, to set partial tasks and check their realization for the purpose of controlling all the processes of registration proceedings.
Registration procedures management: communication with internal and external partners, coordination of procedures.
Legislation/Trends: To monitor legislation as regards a drug regulation as well as developmental trends in the branch for the purpose of implementation of DRA requirements into internal company standards.
University degree in chemistry/natural science/pharmacy.
Previous experience in the regulatory affairs area - at least a year will be an advantage, but we are also open to a motivated fresh graduate.
Decision-making skills, proactive approach, good communication and organizational skills.
Ability to assess and apply legal requirements.
Knowledge of the European DRA legislation might be an advantage.
An opportunity to work for a successful international pharmaceutical company.
An opportunity to learn newest approaches in managing creative and highly adaptive business organizations.
Pleasant and dynamic working environment.
Continuous personal development.
An attractive compensation & benefits package.
Above standard social and benefit program.