ParrotPal Ltd in the UK is seeking a Regulatory Lead with proven MHRA/UKCA experience for software-as-a-medical-device. You will own the MHRA pathway, run the clinical safety case (DCB0129), manage the hazard log and DTAC pack, and provide clinical sign-off on all shipped features.
You’ll chair the clinical advisory board, guard against overclaiming, and work in a founding team that moves quickly with real ownership and fast decisions as the market for GLP-1 health tech expands.
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