(Senior) Manager Drug Regulatory Affairs (m/f/d)

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