Aurora Europe GmbH is the largest authorized importer, exporter, and distributor of medical cannabis in the European Union. We supply high-quality medical cannabis products to patients throughout Europe and have been leaders in the German market since 2015. All our products exceed the high cultivation standards specified under Good Manufacturing Practice (GMP) – meaning we produce and distribute only the safest, highest quality medical cannabis.
Aurora Europe is a subsidiary of Aurora Cannabis, headquartered in Edmonton, Alberta, Canada and traded at the Toronto stock exchange with a market cap of over CAD 12 billion.
As one of the world’s largest and leading cannabis companies Aurora Cannabis Inc. has a funded capacity in excess of 570,000 kg per year and sales and operations in 22 countries across five continents. Aurora is vertically integrated and horizontally diversified across every key segment of the value chain, from facility engineering and design to cannabis breeding and genetics research, cannabis and hemp production, derivatives, high value-add product development, home cultivation, wholesale and retail distribution.
Highly differentiated from its peers, Aurora has established a uniquely advanced, consistent and efficient production strategy, based on purpose-built facilities that integrate leading-edge technologies across all processes, defined by extensive automation and customization, resulting in the massive scale production of high quality product at ultra-low costs. Intended to be replicable and scalable globally, these production facilities are designed to produce cannabis of significant scale, with high quality, industry-leading yields, and ultra-low per gram production costs. Each of Aurora’s facilities is built to meet European Union (EU) GMP standards.
Aurora Europe GmbH is looking for a Berlin based
Senior Manager Regulatory Affairs Europe (m/f/x)
to join our Regulatory Affairs team in the fast-paced cannabis industry. The Regulatory Affairs Manager will lead the regulatory activities within Europe to obtain and maintain product registration status in compliance with european/national laws and regulations, as well as corporate policies and procedures. The Regulatory Affairs Manager will lead and support product registration and serve as the subject matter expert for Regulatory Affairs and provide guidance to local and global business partners. The Manager will develop and implement regulatory strategies to meet project deliverables.