- Preparation of the required documentation and life-cycle management for worldwide registrations of biocidal products, medical devices and cosmetics- Communication and coordination of regulatory activities with Regulatory Affairs departments in the respective countries as well as directly with the authorities in Switzerland- Registration and life-cycle management of drug registrations in Switzerland- Responsible for tasks regarding change management for the regulatory affairs… Show more - Preparation of the required documentation and life-cycle management for worldwide registrations of biocidal products, medical devices and cosmetics- Communication and coordination of regulatory activities with Regulatory Affairs departments in the respective countries as well as directly with the authorities in Switzerland- Registration and life-cycle management of drug registrations in Switzerland- Responsible for tasks regarding change management for the regulatory affairs team- Project lead on the ongoing European wide registrations of Biocides under the regulation 528/2012 (EU BPR)- Leading and collaborating on projects related to new developments, initial registrations and variations of cosmetics, biocide and medical devices- Review and release of labeling specifications regarding the respective regulatory requirements Show less