Technical Writer

Technical WriterCK Group are recruiting for a Quality Systems Technical Writer to join a company in the pharmaceutical industry at their site based in Bracknell, on a contract basis for 12 months.
Salary: Hourly rates in the range of £20.00-£40.00 PAYE, depending on experience.
Quality Systems Technical Writer Role: Responsible for developing and maintaining accurate, clear, and concise procedures, required tools, and resource documents.The role is also responsible for quality checks of the quality system documents to ensure compliance with company standards and procedures.The role manages workflows and metadata in the document control system using Veeva QualityDocs.Responsible for quality systems document management, document architecture, document control in Veeva QualityDocs.Your Background: Bachelor's degree in a relevant field, such as technical writing or life sciences.3+ years of experience in technical writing with a focus on GVP-related documents or related roles in a pharmaceutical or biotech environment.Experience using Veeva QualityDocs or other electronic document management systems (EDMS) preferred.Excellent attention to detail and organizational skills.Strong communication and interpersonal skills.Ability to manage multiple projects and priorities simultaneously.Ability to work well independently and as part of a team within and across culturally and geographically diverse environments.Company: Our client is one of the largest pharmaceutical companies in the world.
They focus on finding answers for some of the world's most urgent medical needs.
Location: This role is fully home based with occasional travel to the offices in Bracknell.