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QA Professional - Pharma Generics
QA Professional – Generics Pharmaceutical ManufacturingLocation: 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
Full UK right to work