Medical Device Quality & Regulatory Specialist

X4 Life Sciences in the United Kingdom is seeking a Quality and Regulatory Co-Ordinator to join their medical device team on a permanent basis. This hands-on, autonomous role focuses on maintaining the ISO 13485 QMS and ensuring regulatory compliance across MDR/UKCA activities.

The ideal candidate has 3–4+ years in a medical device QA/regulatory role, strong CAPA/NCR experience, and proven ability to manage documents, audits, and training records with minimal supervision.

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