We have a clear commitment : putting best-possible solutions in the hands of medical professionals, enabling them to find the right answer to the challenge they face. Fresenius Kabi is a driver of healthcare for the coming decade. We truly live diversity and value different backgrounds and motivations....+ ←
- 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
- 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