Overview
Technical Writer/Pharmaceutical Regulatory Compliance Jobs in Stellenbosch, South Africa at Pillango Placements
Position: Technical Writer (Pharmaceutical Regulatory Compliance)
A Stellenbosch-based company, dedicated to developing
innovative solutions
for healthcare challenges requires a detail-oriented Technical Writer to support the Regulatory Department. If you are a values-driven individual who can make a meaningful contribution that extends beyond day-to-day 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
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Duties
may include:
Technical writing for medical device files Conducting research, literature reviews and writing of research reports 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.
Title: Technical Writer/Pharmaceutical Regulatory Compliance
Company: Pillango Placements
Location: Stellenbosch, South Africa
Category: Healthcare (Clinical Research, Medical Science), Research/Development (Clinical Research, Medical Science)
