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Lieu Pékin, Municipalité de Pékin, Chine Job ID R-050205 Date de publication 05/05/2019

Prepares/agrees/executes global/regulatory tactical submission plans for allocated project/prod that implement the agreed regulatory strategy to develop and maintain products. Provides independent tactical/scientifically related guidance cross functional on aspects of regulatory affairs. Uses knowledge and experience in the regulatory field to influence functional objectives. OR Responsible for the management of a section of a skill group such as CMC, regulatory affairs project management, etc.  Responsible for skill development, performance management, resource allocation.



AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

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Une culture d'entreprise inspirante, des missions riches, des managers qui accompagnent et soutiennent. Des opportunités de rotation rapide au sein de l'entreprise. Ils accordent de l'importance à l'inclusion et à la diversité.