We are looking for an experienced Associate Director Regulatory Affairs to join our growing team in Aachen, Germany. You will ensure the marketability of our products and contribute to our commercial success.
Requirements
- At least 7 years relevant experience within pharmaceutical industry and 5 years' experience within Regulatory Affairs
- Good working knowledge of EU regulatory framework
- Regulatory Life Cycle Management with respect to business needs (CP, DCP, MRP. NP)
- Profound knowledge of EU CTR 536/2014
- Profound experience with CTIS
- Good self-management
- Strong sense of responsibility
- Attention to details
- Ability to connect with internal departments and external partners
- University degree on Science
- Language skills: English - business fluent; fluent in German and/or other EU language is beneficial
Benefits
- An open, appreciative corporate culture
- Short decision-making paths and a high degree of autonomy in your area of responsibility
- Flexible working hours and the option for partial remote work (2 days per week)
- 30 days of vacation and additional benefits
- Modern office building with underground parking in a good location near the highway A44