EU Regulatory Affairs Lead

Experienced Regulatory Affairs professional to lead EU CTR submissions and CTIS lifecycle activities, providing strategic guidance and ensuring compliance.

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals...

IQVIA is seeking an experienced Regulatory Affairs professional in Madrid, Spain to lead and manage EU CTR submissions and CTIS lifecycle activities. You will provide strategic regulatory guidance, interact with regulatory authorities, and mentor junior staff while ensuring timely, compliant deliverables. The role requires 8+ years in regulatory affairs...

Johnson & Johnson Spain (MedTech) seeks a Senior Regulatory Affairs Program Lead & Deputy Technical Responsible to plan, coordinate and deliver regulatory activities ensuring compliance for devices distributed by J&J MedTech in Spain. Focused on Electrophysiology and Neurovascular lines, the role provides senior regulatory guidance to Marketing and...

Almirall is seeking an Associate Director of Regulatory Affairs to lead global regulatory strategies and oversee submissions for development and marketed products. You will partner with Clinical, CMC, Safety, and Market Access teams to ensure timely approvals and lifecycle management across markets.The role requires strong regulatory leadership, extensive...

Johnson & Johnson is seeking a Senior Regulatory Affairs Program Lead & Deputy Technical Responsible for Med Tech. Based in Madrid, you will lead regulatory activities for EU devices, ensuring compliance and timely market access. You will partner with marketing, QA, and operations to interpret regulatory changes and guide cross-functional teams. You will...

Lead regulatory affairs activities for MedTech products in Spain, ensuring compliance with EU and local laws, managing competent authority relations, and providing regulatory guidance.

Johnson & Johnson is seeking a Senior Regulatory Affairs Program Lead & Deputy Technical Responsible for MedTech. Based in Madrid, you will lead regulatory activities for EU devices, ensuring compliance and timely market access. You will partner with marketing, QA, and operations to interpret regulatory changes and guide cross-functional teams. You will...

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays...