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Technical Writer

Eingestellt von Synectics

Projektbeschreibung

SUMMARY:
The position is for a technical writer for the validation projects and remediation projects for regulated GxP and clinical biomarker validations.

PURPOSE:
Provide validation projects with document authoring, managing and final disposition; Provide documentation required for validation remediation projects; Learn software tools to independently produce documents; Manage the hardcopy and electronic documents in appropriate repositories.

RESPONSIBILITIES:
Attend training for the standard operating procedures for validating computer software; Partner with the Project Manager to development documentation for project deliverables, including user requirements, validation plan, test plan, test scripts, validation reports, etc; Convert validation documents to validation documentation format; Become proficient with software tools to independently produce test scripts and user training documents; Work with the software end users to generate test scripts; Complete life cycle of all documents, including drafts, final versions, signatures and document repository; Manage team site in SharePoint; Document change requests.

SKILLS
Analytical Skills, Business Writing/Editing, Pharmaceutical, Project Coordination

Synectics is an Equal Opportunity Employer.

Projektdetails

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

  • Kategorie:

    Sonstiges

Synectics