Nataliya Noreika

QA/RA Manager

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Nataliya has over 10 years’ experience in Quality Assurance (QA) and Regulatory Affairs (RA) of Medical Device, Drug-Device Combination and In-Vitro Diagnostics products, covering all aspects from product concept through regulatory approval into manufacture and ensuring ongoing customer satisfaction.

At Medovate, Nataliya is responsible for the Quality and Regulatory team, not only ensuring that all product and organisational Quality and Regulatory obligations are met, but also that patients and clinicians receive the highest possible standard of safety and clinical performance from their Medovate products.

Nataliya originally graduated with a Master's Degree in Wine making from National Agricultural University, Ukraine, and shortly thereafter a BSc(Hons) in Applied Biosciences and Biotechnology from Cork Institute of Technology, Ireland. She is PRINCE 2 certified in Project Management, a certified lead Quality Systems auditor, member of the Regulatory Affairs Professional Society (RAPS) and holds the RAPS Regulatory Affairs Certificate (RAC) credential for Medical Devices.