Hi, I am looking for a medical writing position. I am currently working in the regulatory department for a medical device company, specifically with post market surveillance reports for products transitioning with EU MDR. I have authored post market surveillance plans/reports and post market clinical follow-up plans/reports. Prior to this, I worked in the company's quality system assessing and providing clinical input for complaints that were received. I have a clinical background as a nurse practitioner and am interested specifically in authoring Clinical Evaluation Reports. I am open to other technical/medical writing positions within the medical device industry. I am also looking for remote work. Thank you for your consideration., Medical Device