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 reports The proposed salary for the role is R20k – R30k but higher can be negotiated for is a perfect fit in terms of experience. The 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.