Jean-Christian Omyale is a regulatory affairs expert, passionate about healthcare technologies with over 10 years of experience in the pharmaceutical and medical device industry.
As a regulatory affairs expert, he is always faced with new challenges regarding standards and regulations in order to bring healthcare solutions to market. He has therefore developed a global vision of software & hardware technologies and a good knowledge of regulatory requirements and applications in the medical field.
With several professional experiences in France, in large groups such as General Electric Healthcare, he worked on the development of complex medical devices and biotech products to create innovative solutions for patient treatment. Since 2017, he moved near Geneva where he worked on different projects in immuno-hematology and radiotherapy.
He is currently working as Senior Regulatory Affairs Manager for Digital Health solutions and Medical Devices at Merck in Eysins, Switzerland. In this role, he is responsible for developing and leading global regulatory strategies for submissions and approvals of medical devices, drug device combinations and digital health products, interfacing with technical, regulatory and commercial teams.
He holds a Biomedical engineering degree from Polytech Lyon, France and also has a professional degree in electrical engineering. He is fluent in French, English and Fon.
