Prepares / executes global / regional regulatory tactical submission plans on allocated projects / products that implement the agreed regulatory strategy to develop and maintain products.
Generates / project manages delivery, to time / quality of submissions. Individuals may start as Regulatory Affairs Assistant and if areas of responsibility change, move to a Regulatory Affairs Specialist role.
Demonstrates in depth knowledge of Regulatory compliances and submissions. Develops and builds good relationships with internal customers and Regulatory authorities, improving Regulatory outcomes.
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.