We are a medical device start-up in Pleasanton, California. We are looking for an intern to assist in collating and assembling some of the documentation we have accumulated thus far to help prepare before we go to market. We are bootstrapping (http://medcitynews.com/2015/04/medical-device-quality-system-musts/?rf=1) and a low-burn start-up (http://leanstack.com/bootstrapping-a-lean-startup/). We are not trying to rocket out the gate.
Either schooling in regulatory affairs, or some modicum of experience. We can train if the basics are available.