
Senior Regulatory Affairs Consultant - Labelling Strategy (home or office based)
Acts as the principal labeling strategist within Global Regulatory Affairs, driving development and maintenance of dCCDS/CCDS, USPI and SmPC, providing labeling input to clinical development and Therapeutic Area teams, and leading Global Labeling Committee assessments. Requires a university degree in life sciences and a minimum of 10 years' biotech/pharmaceutical industry experience (including 6 years labeling/regulatory); fluency in English.











