Due to the upcoming retirement of our colleague, we are looking for a Regulatory Affairs professional to join our regulatory affairs function to be based in Bratislava. This role is a key part of a matrix organization, working closely with colleagues across commercial, market access, medical, Pharmacovigilance and Quality assurance in Slovakia.

In this role, you will:

• Manage regulatory activities for assigned products, including registrations and submission applications
• Work with global vendors and take ownership of translation review, with some translation work performed directly when needed
• Participate actively in brand team meetings for products within the assigned responsibility
• Present product updates, packaging status, pending variations, and expected regulatory decisions to colleagues and leadership
• Support cross-functional colleagues on regulatory topics and day-to-day problem solving
• Handle tasks beyond standard regulatory scope, such as coordinating processes for patient access or special import situations
• Contribute to projects outside routine regulatory work, including AI initiatives 
• Review promotional materials at a basic level
• Collaborate closely with Czech colleagues on bilingual packaging and shared processes