Medtech regulatory affairs lead — eu compliance

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...

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...

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...

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 in Madrid is seeking a Senior Regulatory Affairs Program Lead to oversee planning, coordination and delivery of regulatory activities for MedTech products. You will ensure compliance with EU and local requirements and work with Marketing, Quality and supply teams to keep products compliant and commercially viable. With 4–6 years in...

At Johnson & Johnson,we believe health is everything.Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

Johnson & Johnson MedTech in Madrid seeks a Senior Regulatory Affairs professional to lead planning, coordination and delivery of regulatory activities for EU markets. You will ensure compliance with EU MDR and local laws, interact with authorities, and support product launches across Electrophysiology and Neurovascular lines. The role requires 4–6 years...

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

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