Technical Writer, Technical Author German, FDA, TUV,SOP, SDLC
Technical Writer, Technical Author German, FDA, TUV,SOP, SDLC I have a fantastic opportunity to work within the worlds largest medical device project. Due to the size of the project, I would expect contract extensions. IMPORTANT: I require fluent English and German Project/Department Description and responsibilities: Quality & Compliance; Primary Tasks and responsibilities: - Prepare technical & regulatory documents within established timelines that are of high quality in terms of applicable content, data interpretation, organization, clarity, accuracy, format, and consistency, with adherence...
24-10-2014 - iwantanewjob.ie