QA Officer
Job in
Manchester, Greater Manchester, M9, England, UK
Listed on 2026-08-11
Listing for:
ARx Recruitment Services
Full Time
position Listed on 2026-08-11
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.
As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.
The Role:
Full Time (Monday to Friday) On-site
* Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
* Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
* Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
* Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
* Raising and overseeing the implementation of Change Controls and CAPA's when required
* Participating in site inspections by Regulatory Authorities
* Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
* Writing, reviewing and contributing to Risk Assessments
Benefits:
* Discretional Bonus
* Health Care & More
About You:
* Experience with in a pharmaceutical environment
* A strong Quality Assurance background (2 to 3 years experience)
* Experience with in sterile manufacturing environments (desirable)
* Good working knowledge of GMP requirements and quality systems
* Practical experience in activities of quantitive & qualitive analyses of active substances and of the necessary testing and checking to ensure the quality of medicinal products or associated relevant experience (Ideally)
* Strong communicator and team player
* Confident using Microsoft Office products
If this sounds like a role that you have been looking for, click APPLY NOW
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