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Technical Writer 3 Months Contract

Belmont Lavan Ltd

Application deadline closed.
  • Date posted
    October 21, 2024
  • Location
    Onsite
  • Apply before
    January 31, 2025
  • Career Level
    Any

Job Description

Description

Job description and tasks:

  • Streamline and update all our documentation, currently in version 1.0, to elevate the standards and reflect the latest software version
  • Working in GMP environment and required do strictly adhere to proper quality and compliance standards within QC (Quality Control)
  • Working with a GMP IT software solution within QC (Quality Control)
  • Writing documentation such as: SOPs, User guides, Training material, Continency plan
  • Provide a holistic perspective to our documents and create a functional document structure
  • Handle documentation updates associated with software releases, including the review flow
  • Update documents based on requirements from: end-users, ambassadors, developers, data scientists, SME (QC)
  • Regular input gathering from wide variety of stakeholders: QC stakeholders, IT stakeholders, QA stakeholders
  • Set up a process for an easy documentation update for future
  • Get trained as an editor and take charge of DCCs (Document Change Control)
  • Able to work with high-level of detailed information, but also able to zoom-out and provide the big picture overview

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Skills:

  • Skilled in writing documents (SOPs, user guides, manuals, training materials)
  • Understanding of GMP and adherence to GMP, quality and compliance standards
  • Able to learn new subjects (IT software usage for Quality Control processes within GMP)
  • Detailed oriented, but also able to provide perspective
  • Highly structured
  • Able to ask challenging questions to meet the required quality standards
  • Inquisitive and curious to find answers
  • Problem solving mindset
  • Able to work efficiently in high-paced environment

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Start-date: 1/11-2024

End-date: 31/01-2025 – extension likely

Location: Gentofte Denmark

Requirements

Required skills

Documentation

GMP

Quality Control

Languages

English