Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people’s lives. To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area and platform depth and capabilities – all to bring our medicines to patients even faster. We are seeking key talent, like you, to join us and help give people with disease and their families a brighter future to look forward to.
This role offers hybrid working, requiring 3 days per week in our London office. As Global Labelling Manager (GLM) you will be responsible for the creation and maintenance of regulatory compliant, competitive, and up-to-date core labelling documents for assigned developmental programs and Novartis Innovative Medicines products. The assigned products will be for complex products and may include developmental programs. The RA GLM also provides strategic and operational regulatory labeling input, working in close collaboration with Expert Labeling Task Force (ELTF) members in creating or maintaining core labeling documents. You will also handle Health Authority or Country Operations labeling queries for assigned products.
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives.
Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.