This role is ideal for someone with a scientific or engineering background who can translate technical and clinical information into clear, compliant documentation.
A tertiary qualification in a science, engineering or biological field essential. […]
Experience with medical device or pharmaceutical regulatory requirements would be beneficial (such as MDR 2017/745, FDA 510K, etc)
Ability to write for a regulatory audience
Proficiency in conducting research and report writing […]
Technical writing for medical device files
Conducting research, literature reviews and writing of research reports
The...