Hybrid Regulatory Affairs Manager - Medical Devices (MDR)

A family-owned global leader in medical devices is looking for a Regulatory Affairs Manager to join their hybrid team in Lancashire, UK. This pivotal role involves managing Technical Files and Design Dossiers to ensure compliance with MDD/MDR and ISO 13485 requirements. The successful candidate will lead regulatory compliance activities and risk management, directly influencing the company\’s global operations. A strong background in regulatory affairs within the medical device sector is essential for this position. #J-18808-Ljbffr