Job description
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! The Role: This role can be based in either our White City, London office (hybrid working, requiring 3 days per week) or Novartis site in Schaftenau, Austria> As Global Program Regulatory Manager Medical Devices & Drug/Device Combination Products you will independently provide strategic and operational global medical device regulatory direction and documentation for projects/products. This includes those projects/ products in development, registration and approval/post approval. You will make informed regulatory decisions, balancing patient and business risks and benefits leading to timely Health Authority approvals.
Address
Form of work
London, England
