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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SaMD RA/QA Specialist — Global Regulatory Lead employer: Doccla UK Limited
Doccla is an exceptional employer that prioritises innovation and collaboration in the healthcare sector. With a strong focus on employee growth, we offer opportunities for professional development and a supportive work culture that values diverse perspectives. Working remotely allows for flexibility while contributing to meaningful patient experiences, making it a rewarding place to advance your career.
