Expert, Regulatory Affairs HNC EMEA (fixed-term contract)

The activities linked to the position are highly complex due to the dynamics of the global market and changing regulatory environments and due to business unit changes necessitating license updates. Your responsibility will encompass supporting the HNC regional RA team for a major global roll out activity in cooperation with the HNC RA global segment team. You will be part of a highly professional and motivated team. The role is to be based in Turkiye, hybrid working models (partially) are available. This is a temporary contract and the vacancy is available to 31st December 2026. We are committed to equal employment opportunities and value diversity in the workplace. Being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work to not only benefit our People, Customers & Communities but also drive business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Experienced / skilled in use of related regulatory IT platforms & applications such as Veeva RIMS, Documentum, Trackwise Develop Manage and support the pharma and food submissions (i.e. variations, new registrations, renewals of authorizations or line extensions) in certain regions or countries, with the main focus on Russia re-registration activities Coordinate the submission of dossiers to the regional authorities and follow up on the approval process. Documenting and archiving of submissions and registration statuses in regulatory platforms & applications (software solutions) Support regulatory teams in answering specific customer and/or health authority requests related to product submissions in close cooperation with all internal functions (e.g, QA, Marketing & Sales, Product Management) Support for global standard product document creation, update and maintenance