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Nadeem Omer-Jin is a seasoned professional in regulatory affairs and quality engineering with extensive experience within the medical device industry. Currently serving as a Senior Regulatory Affairs Specialist at Baxter International Inc. since January 2020, Nadeem leads EU regulatory efforts for multiple subsidiaries and provides strategic regulatory support aligning with EU MDR requirements. Previous roles include Senior Regulatory Affairs Specialist at Stryker, where responsibilities encompassed pre-market regulatory activities and technical documentation preparation, as well as a Quality Engineer role focused on design assurance. Nadeem's career began at Baxter International Inc., where contributions included quality assurance support and document control management. Educational background includes a Master of Chemistry with Honours from Kingston University and prior qualifications in science and applied science from Kingston College and Harrow Weald College.