Your main tasks: Regulatory support of international pharmaceutical marketing authorisations Planning, implementation and coordination of European procedures (MRP/DCP) Strategic planning and implementation of variations in and outside Europe Establishing and maintaining relationships with regulatory authorities and relevant third parties Supporting the local market units in terms of regulatory tasks Participating in projects by contributing regulatory expertise Monitoring the regulatory environment and assessing its relevance for the product portfolio Your profile: You have a completed University degree in sciences You bring at least 3 years of work experience in European and international drug regulatory affairs You have a structured working style, you are detail-oriented, a team player and a problem solver You are known for your high level of precision and strategic thinking You have very good communication skills You have very good English language skills (written & spoken) You have good IT skills and an interest in regulatory IT topics