Regulatory & Quality Lead, Medical Devices/IVD (12M)

Mitra Bio in London is seeking a Regulatory Affairs & Quality Manager to lead regulatory and quality activities for our melanoma diagnostic programme, including a non-invasive sampling device and a sequencing-based test. You will prepare technical documentation, manage our QMS, and act as Mitra Bio’s regulatory contact with UK and EU authorities, Notified Bodies and partners.

You’ll ensure regulatory requirements are incorporated throughout development and that evidence meets submission

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