QA & Regulatory Affairs Specialist — Medical Devices

Pangaea Data Limited seeks a Quality Assurance & Regulatory Affairs Specialist to own and continuously improve our QMS as the company scales. You will lead quality processes, drive regulatory documentation, and collaborate with product, engineering, and clinical teams to embed compliance across development.

Ideal candidates bring 2–5 years in medical device/digital health QA, with hands-on ISO 13485 experience and exposure to CE marking or regulatory submissions.

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