UK & Ireland Regulatory & Quality Leader (Medical Devices)

Dormont Manufacturing Co is seeking a Quality & Regulatory Affairs Manager for the UK and Ireland. This pivotal role oversees regulatory compliance and quality systems in line with ISO 13485. The successful candidate will lead the UKI QRA team, ensuring adherence to UK and EU regulatory standards.

Responsibilities include managing regulatory submissions, coordinating audits, and providing regulatory expertise for local projects. This role offers a competitive salary and a variety of benefits designed to support employees throughout their careers.