A BDN client is looking for a Post Market Quality Engineer with 3-5+ years of experience within the Medical Device Industry who will be working within the Post Market Quality team reviewing complaints and technical write-ups that Engineers have written. This individual will be interacting with complaint handlers to making sure the write-ups are in compliance, and that the complaints have been addressed properly. The consultant may be required to write letters that summarize the findings of the investigations and closing out the complaints if needed. This candidate must have Medical Device experience (Class II at minimum), complaints, and be familiar with FDA requirements (21 CFR Part 803/806), as well as Design controls. The ideal candidate would have Class III Device experience (Neurovascular Implants, Stents, Catheters), and have an Engineering degree. This is not solely a complaint handling role, it is a more technical, review type role.