Quality Control Analyst – Pharmaceutical GMP

About the role

Our client, a growing pharmaceutical manufacturing organisation in Kent, is seeking a Quality Control Analyst to join their Quality team. This permanent, full‑time position offers broad exposure to QC activities and regular collaboration with QA and Production, providing a supportive environment for professional development.

Key responsibilities

• Perform HPLC and other analytical tests on raw materials, in‑process samples, and finished products.
• Support manufacturing schedules by completing QC activities within required timeframes.
• Review and interpret analytical data to ensure compliance with quality standards.
• Assist with laboratory investigations, troubleshooting, and problem‑solving.
• Maintain laboratory equipment and uphold high standards of housekeeping and regulatory compliance.

Required profile

• Previous experience in a GMP‑regulated Quality Control laboratory.
• Hands‑on experience with HPLC analysis and related laboratory techniques.
• Strong understanding of GMP requirements and laboratory documentation practices.
• Ability to communicate analytical results clearly and effectively.
• Problem‑solving skills and experience supporting laboratory investigations.

Required skills

• HPLC
• GMP
• Analytical testing