QA Professional – Pharma Generics

4759726
  • Job type

    Permanent
  • Location

    Watford
  • Working Pattern

    Full-time
  • Specialism

    Quality Assurance And Validation
  • Industry

    Pharmaceuticals
  • Pay

    £45000

QA Officer Pharma Generics

QA Professional – Generics Pharmaceutical Manufacturing
Location: London | On‑site: 5 days per week | Type: Permanent

Your new company
This organisation is a well‑established generics pharmaceutical manufacturer supplying regulated markets across the UK and Europe. With a strong focus on compliance, quality systems, and continuous improvement, the business offers a stable, professional environment where quality plays a central role in commercial success. You will be joining a collaborative site that values rigour, accountability, and right‑first‑time execution.

Your new role
As a QA Professional, you will play a key role in maintaining GMP compliance across site quality operations. Your responsibilities will include:
  • Reviewing batch manufacturing and packaging documentation to ensure accuracy, completeness, and GMP compliance
  • Performing detailed document and data review to support batch disposition and release activities
  • Managing and supporting investigations, including deviations, CAPAs, and root cause analysis
  • Coordinating and assessing change controls in line with internal procedures and regulatory expectations
  • Supporting the maintenance and continuous improvement of the Quality Management System (QMS)
  • Liaising closely with Manufacturing, QC, and Supply Chain to resolve documentation and quality issues
  • Supporting audit readiness and contributing to inspection preparation activities

What you’ll need to succeed
To be considered for this role, you will need:
  • 5–8 years’ experience in a Quality Assurance role within pharmaceutical manufacturing
  • Strong hands‑on experience with batch record review and GMP documentation
  • Proven experience managing deviations, CAPAs, and change control processes
  • Solid working knowledge of EU/UK GMP requirements and data integrity principles
  • Experience operating within a regulated quality system environment (electronic or paper‑based)
  • High attention to detail and the ability to manage competing priorities to deadlines
  • Confident communication skills and the ability to work cross‑functionally in an on‑site setting

Apply for this job

Talk to Alex Speakman, the specialist consultant managing this position

Located in London-City, 5th Floor, 107 Cheapside, Telephone +44 333 010 6403
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