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.
Apply today and welcome to where we thrive together!
As Global Labelling Manager (GLM) you will be responsible for the maintenance of regulatory compliant, competitive, and up-to-date high quality and timely implemented core labelling documents (incl. Core Data Sheet (CDS)) and key country labelling (incl. US and EU) for assigned Novartis Innovative Medicines products.
The assigned products will include higher complexity products and may include developmental programs.
The RA GLM provides strategic and operational regulatory labelling input, working in close collaboration with Expert Labelling Task Force (ELTF) members in maintaining core labelling documents, key labelling, and for handling Health Authority or Country Operations labelling queries for assigned products.
Job Description
Key Accountabilities:
This role offers hybrid working, requiring 3 days per week / 12 days per month in our office.
As Global Labelling Manager , you will be responsible for :
Maintaining regulatory compliant, competitive and up-to-date global labelling documents for assigned products, leading the ELTF to align on labelling strategy, labelli ng course of action and text.
Representing G lobal L abelling in relevant sub-teams, research ing and providing input about labelling topics across different markets, the competition, and regulations.
