6+ months 40 hours a week
Our medical device client is looking for a regulatory tech writer to help out with numerous projects that are going on. The most urgent deadline is for a literature search protocol and then doing the literature search and writing the report as well. The main need from this person will be to understand basic research skills and have a strong background in technical writing. Average tasks will be preforming literature searches, taking a look at guidance documents for different medical device submissions and then writing those submissions. The preference would be for someone who has medical device experience for FDA submissions as well as EU.
- Experience outweighs degree
Nice to Have
- Experience writing for a De Novo, IDE, or 510k
Remote: Regulatory Tech Writer – Device (234160)