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 and SDLC standards/guidelines
- Writing CSV documentation 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
- perform test scripts
Requirements (Must have):
- Expertknowledge in matters of computersoftwarevalidation
- Knowledge of ISO Regulations
- Knowledge of SDLC (Software Development Lifecylce)
Beginn: 13.10.2014
Dauer: 28.12.2014
Branche: Medizin/Healthcare