QA Professional - Pharma GenericsHays Life Sciences • North Acton, England, United Kingdom
QA Professional - Pharma Generics
Hays Life Sciences
- North Acton, England, United Kingdom
- North Acton, England, United Kingdom
Über
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
Sprachkenntnisse
- English
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