Job Description Do you have experience in all aspects of a Regulatory Affairs project, supporting technical/ CMC, clinical, nonclinical and procedural aspects of strategy and submissions, but are looking to take this to the next level, supporting a best in class vaccine as we expand into new markets and maintain current licenses ? As part of the Global Regulatory Affairs

Job Description Are you a subject matter expert in technical / CMC and procedural aspects of Global Regulatory Affairs, driven to provide in depth input into asset specific regulatory strategy on a global scale for clinical/labelling or technical/NC or procedural aspects? Are you driven to provide robust regulatory advice and plans to various project teams and advisory bo