*Working with a dynamic team to navigate the current Regulatory Landscape
*Research of international regulatory requirements and guidelines for relevant changes
*Execution of European and international medical device approval and registration procedures
*Communication with internal and external parties
*Active participation in cross-functional and international projects
*Looking at Regulatory strategy
*Working with products ranging from Class I, II, IIB and III including
o Including injectables, Pumps, Cartridges and other drug delivery systems
Skills and Experience Required
-Completed scientific, medical, engineering, or technical studies or other relevant education
-Thorough understanding of the regulatory landscape for combination devices
-5+ year's experience of working with combination products
-MDR experience essential
-Experience with the National Medical Products Administration (NMPA) Formerly the CFDA would be beneficial
-Fluent English required (Another European Language is Beneficial)
How to apply
Apply here if you are interested in this opportunity please apply on the link below or if you would like a confidential discussion about your career opportunities please contact Isabel Kennedy of EPM Scientific.
