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AD Global Regulatory Affairs
500 million patients were touched by Sandoz generic and biosimilar medicines in 2021 and while we're proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world. How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. The Associate Director Global Regulatory Affairs is responsible for regulatory and strategic leadership to assigned biosimilar/biotech projects. You will also be responsible to prepare, compile high quality documentation for complex global regulatory submissions in various countries. For our team in


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