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Theramex Warsaw Mazowieckie Poland (Hybrid)
You are expected to be a Regulatory Affairs Professional with some work experience in Regulatory Affairs/Pharmaceutical industry (minimum 1 year and preferably with an understanding of CMC documentation/Module 3). It is expected that you will be eager to learn have good interpersonal skills and problemsolving capabilities and be able to work on several issues within matrix environment. You will also be able to demonstrate excellent attention to detail and be fluent in English (both written and spoken).
About you:
You have a degree in Pharmacy Biology Chemistry or related disciplines with some work experience in Regulatory Affairs or Pharmaceutical industry. You have some understanding of National and European procedures in DCP MRP and Centralised Procedure and you are keen to learn new things.
About the role:
We are looking for a (Junior) Regulatory Affairs Product Specialist located in Poland to work in the Global Regulatory Affairs team supporting activities in European and international markets. You will provide regulatory support related to the designated products and help implement regulatory strategy with support and supervision from other team members.
Main accountabilities include:
Theramex is a company dedicated to womens health across key times in their lives. We work with Passion Agility Collaboration and Integrity. This means:
Full Time