
Regulatory Affairs Consultant Labelling - German Speaker m/f/d
Responsible for end-to-end labelling lifecycle, CCDS development and maintenance, preparing and reviewing labelling for regulatory submissions and variations, maintaining labelling databases, supporting global harmonization, and collaborating with regional teams. Requires life-science degree, several years in biotech/pharma with global labelling responsibilities, direct Swissmedic experience, and fluency in German and English.












