Technical Author – Medical Devices
Biotechnology Chemical Clinical Life Sciences Pharmaceuticals
Location Wiltshire or Home Based
An exciting opportunity has become available for a technical author / specification writer, for a
leading medical devices organisation.
In the role you will be responsible for preparing medical device manufacturing documentation, and validation reports. Ideally you will be experienced with technical writing which supports medical device manufacturing process and design transfer, and have a comprehensive understanding of design controls, risk management processes and QMS.
An understanding of the principles of design for manufacture, MDD and MDR, and knowledge of document management systems would be highly desirable.
This is an exciting role where you will be liaising with internal and external colleagues globally.
The role can be home based but does require some on site presence at their Wiltshire Technology Centre.