QA Officer – Pharmaceutical Manufacturing
Location: Cheshire
Salary: Competitive + Benefits
Our client is a rapidly expanding pharmaceutical manufacturing company based in Cheshire, operating within GMP-regulated cleanroom environments. Due to continued growth, they are looking to appoint a QA Officer to support Quality Assurance activities across the site.
This role will focus heavily on Quality Management Systems (QMS), including deviations, CAPAs, change controls, documentation review, and cleanroom environmental monitoring activities.
Key Responsibilities
* Support and maintain the site QMS in line with GMP requirements
* Manage deviations, CAPAs, change controls, and quality events
* Review GMP documentation including SOPs and batch records
* Perform and trend cleanroom environmental monitoring activities
* Support audits, inspections, and continuous improvement initiatives
* Work cross-functionally to ensure quality and compliance standards are maintained
Requirements
* Previous QA experience within a pharmaceutical GMP environment
* Experience with QMS activities including deviations, CAPAs, and change controls
* Understanding of cleanroom operations and environmental monitoring
* Knowledge of EU GMP standards
* Strong communication, organisation, and problem-solving skills
This is an excellent opportunity to join a growing pharmaceutical business offering long-term development and career progression within a fast-paced manufacturing environment