The Regulatory Operations Specialist plays an essential role in a team that works across the relevant classification regulations to deliver high quality registration packages efficiently. You will ensure appropriate levels of detail within the files for internal purposes, external registrations, and ongoing maintenance activities throughout the full product lifecycle. You will ensure business agility in manufacture and supply activities and will strive to maintain an excellent level of compliance for our products globally.
You will enable regulatory operations delivery of global projects and programs for our existing brands by providing key skills and expertise in dossier creation.
You will ensure that all regulatory dossier activities are completed according to the best process, in a consistent approach across projects. You will work alongside a wide range of cross functional stakeholders including the RAS Global function, Medical, R&D, Supply, Quality and Marketing.
