Technical Writer
2 months ago
Salary:
Hourlyrates in the range of 20.00- 40.00 PAYE, depending onexperience.
Quality Systems Technical WriterRole:
- Responsible fordeveloping and maintaining accurate, clear, and concise procedures,required tools, and resource documents.
- Therole is also responsible for quality checks of the quality systemdocuments to ensure compliance with company standards andprocedures.
- The role manages workflows andmetadata in the document control system using VeevaQualityDocs.
- Responsible for quality systemsdocument management, document architecture, document control inVeevaQualityDocs.
YourBackground:
- Bachelor sdegree in a relevant field, such as technical writing or lifesciences.
- 3 years of experience in technicalwriting with a focus on GVP-related documents or related roles in apharmaceutical or biotechenvironment.
- Experience using Veeva QualityDocsor other electronic document management systems (EDMS)preferred.
- Excellent attention to detail andorganizational skills.
- Strong communication andinterpersonal skills.
- Ability to managemultiple projects and prioritiessimultaneously.
- Ability to work wellindependently and as part of a team within and across culturallyand geographically diverseenvironments.
Company:
Our client is one of the largest pharmaceutical companies in theworld. They focus on finding answers for some of the world's mosturgent medical needs.
Location:
This role is fully home based with occasional travel to the officesin Bracknell.
Apply:
It is essential that applicants hold entitlement to work in the UK.Please quote job reference 105651 in allcorrespondence.
Pleasenote:
This role may be subjectto a satisfactory basic Disclosure and Barring Service (DBS)check.
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