Junior regulatory affairs specialist

Work with RA colleagues and manufacturing sites RA teams to obtain required documentation per local country regulations.

Prepare and submit regulatory files and documentation to Regulatory Authorities in CIS in accordance with local country regulatory requirements.

Interact with translation agencies to obtain Russian translations of registration documentation.

Ensure timely approval of new IVD medical devices and continued approval of marketed products.

Support the local Commercial team with registration documentation for local tenders.

Interact with our business partners and regulatory agency to expedite approval of pending registration.

Provide metrics and feedback to management as required, keep company’s databases up to date to enable trac...