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, internal guidelines/ styles/processes, and SDLC standards/guidelines
- Writing GxP relevant technical SOP's (procedures) for Softwareproducts 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
Technology that need to be upgraded:
- JDE
- Oracle
- Data Mirror (IBM Software) ? ?CDC Infos4?
- Transform
- ADAPTIV (e-Matrix)
Requirements (Must have):
- Master and/or Bachelor Degree in Mathematics, Engineering, Computer Science, Chemistry or Bioinformatics OR equivalent through experience.
- Advanced course work in technical systems plus continued education in technical disciplines is preferred
- Profound knowledge within Software Dev. Lifecycle Process
- Profound knowledge within Softwarevalidation
- Accepts personal responsibility for client satisfaction
- Strong tracking, coordination and project planning skills
- Establishes and manages engagement objectives, expectations and quality plan
- Ability to identify and implement process and/or application improvements
- Strong analytical and problem-solving skills
- Must be able to work on multiple simultaneous tasks with limited supervision
- Quick learner, motivated self-starter
- Excellent customer service, interpersonal, communication and team collaboration skills
- Able to follow change management procedures and internal guidelines
Environment/Miscellaneous:
- flexibel working hours / Parttime
Beginn: 01.04.2014
Dauer: 31.12.2014
Branche: Medizin/Healthcare