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Technical Writer - Medical Devices - Switzerland

Eingestellt von Templeton and Partners

Projektbeschreibung

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)

Projektdetails

  • Einsatzort:

    Solothurn, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    Keine Angabe

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

  • Kategorie:

    Sonstiges

Templeton and Partners