Technical Writer
2 days ago
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.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 105651 in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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