Lead and develop a high-performing Regulatory Affairs team to secure timely market authorisations
Drive process optimisation and act as a trusted regulatory partner to internal and external stakeholders
Support the strategic direction, execution, and optimisation of regulatory development activities for the country
Ensure timely regulatory submissions and drive KPI performance
Serve as a key contact for health authorities in collaboration with colleagues across the organisation
Coordinate cross-functional input and ensure full adherence to regulatory requirements while enabling commercial objectives
Manage team capacity, resource allocation, and performance delivery against KPIs
Foster employee engagement, development, and retention within the team

Demonstrated professional experience in Regulatory Affairs within pharma, biotech, or a related healthcare setting
Solid hands-on experience with regulatory submissions, licensing, and compliance processes
Bachelor’s or Master’s degree in Life Sciences, Pharmaceutics, Regulatory Affairs, or equivalent
Minimum 3+ years in a leadership position , within pharma/biotech or pharma services
Experience working with structured administrative and documentation processes
Fluent English, written and spoken
Practical knowledge of artwork/design tools (InDesign, Illustrator, Photoshop) is a plus
Residence in Spain and a valid work permit

Manager, Regulatory Affairs

Key skills