TRABAJO MEDICAL AFFAIRS FLORIDA DE LIÉBANA, SALAMANCA

Previous medical device submission experience preferred... fda regulations and european medical device regulations (and previous medical device directives) is required...

Global strategic marketing, medical affairs, regulatory affairs, r&d, etc... position summary the principal clinical research scientist for the surgical vision platform...

Solid understanding of applicable fda (qsr) regulations, canadian medical device regulation (cmdr), medical device regulation (mdr), iso, and iso is strongly preferred...

Preferred: working experience with complex medical device systems and exposure to different types of medical device manufacturing... experience and skills: required:...