Descripción de la oferta
The opportunityInscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación.As our Manager, Regulatory Affairs HUB SoE, you will support the strategic direction, execution, and optimisation of regulatory development activities for the country. This is a hands‑on leadership role requiring strong subject‑matter expertise in Regulatory Affairs and proven experience managing a team of more than four employees.You will ensure timely regulatory submissions, drive KPI performance, and serve as a key contact for health authorities in collaboration with colleagues across the organisation. You will lead and develop a team of regulatory professionals, coordinate cross‑functional input, and ensure full adherence to regulatory requirements while enabling commercial objectives.We would like you to:As Deputy Manager, you will be responsible for delivering regulatory outcomes through effective leadership, operational oversight, and regulatory expertise within a highly regulated pharmaceutical environment.In this role, you will:Lead PI (parallel import) license applications and ensure their ongoing maintenanceTranslate strategic regulatory objectives into actionable operational plansDevelop and optimise the parallel distribution marketing authorisation functionGuide the team through complex regulatory processes, ensuring compliance across marketsMaintain ownership of internal procedures, ensuring they remain current, compliant, and continuously improvedManage team capacity, resource allocation, and performance delivery against KPIsFoster employee engagement, development, and retention within the teamContribute actively to change management initiatives that improve efficiency and regulatory alignmentAbout you, our new colleague:You are a confident and communicative leader with deep experience in Regulatory Affairs and a strong track record of managing and developing teams. You thrive in structured, compliance‑driven environments and combine technical expertise with pragmatic stakeholder engagement. xcskxlj What we require from you:Demonstrated professional experience in Regulatory Affairs within pharma, biotech, or a related healthcare settingSolid hands‑on experience with regulatory submissions, licensing, and compliance processesBachelor’s or Master’s degree in Life Sciences, Pharmaceutics, Regulatory Affairs, or equivalentMinimum 3+ years in a leadership position, within pharma/biotech or pharma servicesExperience working with structured administrative and documentation processesFluent English, written and spokenPractical knowledge of artwork/design tools (InDesign, Illustrator, Photoshop) is a plusResidence in Spain and a valid work permitThe position is based in Madrid, and you are expected to be present in the office a minimum of 3 days per week.#J-18808-Ljbffr
