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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QA & Regulatory Affairs Specialist — Medical Devices employer: Pangaea Data Limited
Pangaea Data Limited is an exceptional employer, offering a dynamic work environment in the heart of London where innovation meets healthcare. Employees benefit from private medical insurance, life insurance, and travel cards, while also gaining invaluable experience in a fast-growing startup alongside seasoned professionals. With a strong emphasis on employee growth and a collaborative culture, Pangaea empowers its team to make a meaningful impact on patient outcomes through cutting-edge AI technology.
