MedTech QA/Regulatory Associate — ISO 13485 & FDA Prep

ScubaTx Limited is seeking a hands-on Quality & Regulatory Associate to support the execution of our QMS and regulatory activities as we progress ISO 13485 readiness and FDA 510(k) preparation. This role is execution-focused, supporting external QA/RA consultants and internal teams to ensure documentation, design controls and quality processes are implemented accurately and on time.

This is a junior–mid level position with flexible working arrangements in Manchester and opportunities to grow

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