Regulatory & Quality Lead, Medical Devices (UK & IE)

Medtronic Ltd. in the UK and Ireland seeks a Quality & Regulatory Affairs Manager to lead regulatory compliance, post-market surveillance, and ISO 13485 alignment.

You'll oversee the UKI QRA team, serve as primary contact with MHRA/HPRA, and drive regulatory strategy across UK/EU regions, ensuring local projects meet requirements.

Role emphasizes cross-functional collaboration, audits, and continuous improvement of quality systems to support patient safety and business goals.