Do you want to work broadly with Regulatory Affairs in an international pharmaceutical company where you will combine operational regulatory work with process improvements, stakeholder management, and technical ownership?
We are looking for an experienced Regulatory Affairs Specialist to join our South of Europe HUB in Madrid. Here, you will become part of a growing international setup supporting multiple European markets while working closely with colleagues across Regulatory Affairs, QA, Product Development, and Operations.
You will join the Regulatory Affairs South of Europe HUB - a team responsible for handling submissions, approvals, and lifecycle management of parallel import licenses across several European markets.
The team currently consists of two Regulatory Affairs Specialists based in Madrid, working closely together in a highly collaborative and international environment. The role combines operational execution with o...