A Stellenboschbased company dedicated to developing innovative solutions for healthcare challenges requires a detailoriented Technical Writer to support the Regulatory Department. If you are a valuesdriven individual who can make a meaningful contribution that extends beyond daytoday responsibilities we would like to hear from you!
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 candidates qualifications skills and experience.
NOTE: We ONLY accept online applications. We do not consider direct applications via Whatsapp or email.