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 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):
- Experience in validation of ERP, MES, LIMS, WMS in pharma/MD industries;
- 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;
- Able to follow change management procedures and internal guidelines.
Environment/Miscellaneous:
- full-time onsite
Beginn: 01.10.2018
Dauer: 31.12.2018
Branche: Medizin/Healthcare