Beschreibung
Task:- 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 to regulatory guidelines, our customer´s internal guidelines/ styles/processes, and SDLC standards/guidelines
- Writing technical SOP's (procedures) and work instructions based on input from the different technical departments and based on available documentation/ presentations
- Perform technical writing, research, and related editing functions to prepare documents, test plans, user cases, project manuals, business proposals, reports, briefings, presentations, guidelines, and other written materials
Requirements (Must have):
- SDLC GRQP Support:
- Erfahrung mit Subversion und Polarion von Vorteil
- Erfahrung mit SDLC von Vorteil
- Erfahrungen im Bereich CSV (wünschenswert)
- Sehr gutes Englisch & Deutsch in Wort und Schrift ist Grundvoraussetzung!
Beginn: 07.07.2014
Dauer: 28.12.2014
Branche: Medizin/Healthcare