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Quality Assurance Officer

Job in Preston, Lancashire, SN15, England, UK
Listing for: ARx Recruitment Services
Full Time position
Listed on 2026-08-17
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 32000 - 45000 GBP Yearly GBP 32000.00 45000.00 YEAR
Job Description & How to Apply Below

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

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 QA 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
  • Strong communicator and team player
  • Confident using Microsoft Office products
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