SaMD RA/QA Specialist — Global Regulatory Lead

Doccla UK Limited is hiring a Regulatory Affairs Specialist for its SaMD portfolio. You will manage EU/UK MDR technical documentation, risk management, and labeling compliance, ensuring regulatory readiness across markets. The role supports changes, PMS, and vigilance activities.

You will work in a hybrid model with London presence, collaborating with Engineering, Clinical and Quality teams to maintain compliance and timely submissions.

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