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Yasser Zayni began their work experience in 2009 as a Senior Medical Device Specialist at the Medicines and Healthcare products Regulatory Agency. In this role, they were responsible for risk assessment of medical device failures, reviewing safety notices, and collaborating with regulatory agencies worldwide. From 2016 to 2017, they worked as a Regulatory Affairs Consultant at Bausch + Lomb, where they ensured post-market quality and regulatory requirements were met. In 2017, they moved to Zimmer Biomet as a PMS & QMS Consultant, overseeing post market remediation activities and complaint handling. In the same year, they also joined BD as a Regulatory Compliance Specialist, providing support to the Regulatory Compliance team. Currently, Yasser is the Vice President of Product Management at Signifier Medical Technologies Ltd, taking on responsibilities in the areas of product management and regulatory compliance.

Yasser Zayni obtained a Master's Degree in Medical Electronics and Physics from Queen Mary University of London, from 2013 to 2015. Prior to that, they completed an Engineer's Degree in Biomedical/Medical Engineering from the same university, between 2004 and 2008. Additionally, in December 2017, Yasser obtained certification as a Medical Devices Management System Lead Auditor using ISO 13485:2016 from Exemplar Global, Inc.