Beschreibung
Technical Writer - Medical Devices - Switzerland
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, 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
Experience with IT Disaster Recovery and/or Change Management processes is a plus
Strong tracking and coordination 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
English spoken and written
German is a plus
IT IS ESSENTIAL TO UTILISE SWISS PAYROLL SOLUTIONS (NO LIMITED COMPANIES)