(temporary replacement during 12 months due to parental leave)

The International Regulatory Affairs Manager is responsible within Avextra Pharma GmbH for the compilation of regulatory documents for new products. To this end, the International Regulatory Affairs Manager collaborates on all measures necessary to obtain approval from international authorities for the development, manufacture, marketing, and distribution of the products. It is the responsibility of the International Regulatory Affairs Manager to demonstrate the safety, quality and efficacy of products to various international regulatory authorities and to demonstrate that international regulations, procedural guidelines and principles are being followed.

Tasks and responsabilities:



Sabrina Knab

E-Mail: careers@avextra.com