Are you passionate about ensuring regulatory compliance and navigating the complexities of regulatory frameworks? Do you want to play a key role in gaining approvals for new drugs while safeguarding patient safety? If so, we are looking for a dedicated Regulatory Affairs Specialist to join our team in Kazakhstan.

Your new role

In the role of Regulatory Affairs Specialist, you will facilitate the registration of new medicines and life-cycle management, labelling updates, safety variations for NN portfolio in Kazakhstan. It's a temporary position.

You will develop goals and deliverables that are aligned with business priorities in collaboration with management and stakeholders, while driving the submissions and approvals in the scope of the position.

Moreover, you will monitor regulatory requirements changes, ensure alignment with internal SOPs and local legislation, maintain accurate use of regulatory IT systems (Vault RIM, NovoDocs, LIFT) while ensurin...