Quality Assurance Officer – Pharmaceutical GMP

About the role

We are seeking a Quality Assurance Officer to join a fast‑growing pharmaceutical manufacturer that supplies active pharmaceutical ingredients and specialist products. The role is based in Kent and offers the chance to work across the full QA lifecycle within a GMP‑regulated environment.

Key responsibilities

• Maintain and continuously improve the Quality Management System (QMS).
• Review and approve batch manufacturing documentation prior to product release.
• Review and approve SOPs, controlled documents and quality records.
• Manage quality events such as deviations, CAPAs, change controls, complaints and out‑of‑specification investigations.
• Support internal audits, supplier audits and ongoing compliance activities.
• Assist with preparation for customer and regulatory inspections.

Required profile

• Previous experience in a GMP‑regulated Quality Assurance environment.
• Strong understanding of GMP and broader GxP requirements.
• Experience with Quality Management Systems and related documentation.
• Knowledge of CAPA, deviation handling, change control and batch record review processes.
• Eligibility to work in the United Kingdom.

Required skills

• GMP compliance
• Quality Management System (QMS) handling
• CAPA management
• Deviation and change control processes
• Batch record review