Beschreibung
A top 5 Medical Device company based in Switzerland require an IT Technical writer to join their Quality/Compliance & IT infrastructure department on a contract basis.
Primary 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 to regulatory guidelines, J&J 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 related to IT Infrastructure
- 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:
- Strong experience in regulated environments, especially in CSV and GxP
- 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