At KRKA Spain, a member multinational pharmaceutical company, present in over 70 countries and leader in the production and distribution of medicines, we are looking for a Regulatory Associate to join our team.

Key Responsibilities:

- Monitoring and managing product registration regulations
- Preparing regulatory activity plans for individual products
- Preparing, in cooperation with expert departments at Krka, the registration documentation and translations into local language
- Submitting registration documentation to the relevant state institutions in order to be granted marketing authorisation as soon as possible
- Conducting registration procedure – supporting the procedure during all phases
- Providing on-going information about problems in obtaining marketing authorisation (in writing)
- Participating in the organisation and/or realisation of document and text translations into local language




- Checking and making corrections of packaging materials written in local language intended for submission to regulatory authorities and before final print
- Organising, providing guidance and keeping records on receipt, distribution and archiving of internal and external documentation, information and data
- Keeping the data base and documentary records on the registration procedures and distributing relevant data concerning the marketing authorisations
- Setting up and maintaining the information system for the entire product range in the territory
- Monitoring, analysing and assessing work results
- Submitting the pharmacovigilance documentation to the relevant state institutions and

📌 Regulatory affairs associate (España)
🏢 Krka
📍 España