Technical Writer

CK 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.


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.