Qa Professional – Pharma Generics

QA Professional – Generics Pharmaceutical Manufacturing Location: London | On‑site: 5 days per week | Type: Permanent
Your newpany This organisation is a well‑established generics pharmaceutical manufacturer supplying regulated markets across the UK and Europe. With a strong focus onpliance, quality systems, and continuous improvement, the business offers a stable, professional environment where quality plays a central role inmercial 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 GMPpliance across site quality operations. Your responsibilities will include:Reviewing batch manufacturing and packaging documentation to ensure accuracy,pleteness, and GMPpliance
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 managepeting priorities to deadlines