Senior/Team Lead International Regulatory Affairs (gn)

• Overall responsibility for all approval processes (incl. life cycle management) in approx. 35 countries worldwide
• Management and further development of the 12-strong team
• Developing the approval strategy for the region, including meeting deadlines through targeted prioritization
• Main contact person for Business Development and Market Access in order to achieve overarching goals and make decisions
• Close coordination with authorities, including occasional on-site presence
• Close interface coordination as part of the approval process

• Successfully completed scientific studies
• Relevant experience in international marketing authorization of medicinal products
• Initial management experience desirable – but can also be developed on site
• Strong analytical and forward thinking skills
• Fluency in English
• Good knowledge of German
• Ideally good knowledge of French
• Willingness to travel globally (approx. once a month)

• A wide range of development opportunities
• Employee benefits, such as fitness allowances and much more
• Regular team events and numerous company celebrations
• Firmly anchored and „lived“ corporate culture
• 40% mobile working
• 30 days vacation per year

Gender-Hinweis

Geschlechter.