Description:
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.
Skills and Experience:
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 Basic knowledge of the human anatomy Strong attention to detail Duties may include:
Technical writing for medical device files Conducting research, literature reviews and writing of research reportsThe final remuneration package will be based on market standards, considering the candidate's qualifications, skills, and experience.
NOTE: We ONLY accept online applications. We do not consider direct applications via Whatsapp or email.
28 Mar 2025;
from:
gumtree.co.za