A background in medical devices is preferred and with a minimum of 5 years regulatory experience with worldwide registrations, and with Japanese language and submissions experience a definite bonus. A background in Polymer Science/ Chemistry is also suitable, as is Pharmaceutical with some working experience in Medical Devices. You will show product awareness and knowledge of respective regulatory frameworks, excellent planning and organisational skills, and be able to converse confidently with regulatory authorities and multi-disciplinary product development teams worldwide.
Occasional travel will be required
For more information on this vacancy, or any other medical device opportunities, please contact the Senior Consultant Andrew Boroky on 0044 (0) 207 940 2116, or email him at email@example.com
Posted: 08/08/2012 | NPJ Ref: 84797