Quality Control Analyst (QC Analyst)

Quality Control Analyst

Join a leading pharmaceutical manufacturing organisation to play a key role in ensuring the quality and release of medicines supplied to patients worldwide. As part of a busy analytical laboratory team, you will perform routine and stability testing of pharmaceutical products within a GMP-regulated environment. Your work will involve conducting analytical testing, supporting investigations, maintaining laboratory equipment, and helping ensure products meet the highest quality standards.

Key Responsibilities

• Perform routine and stability testing of pharmaceutical products.
• Conduct analytical testing using techniques including HPLC, Karl Fischer, dissolution, and other physical and chemical methods.
• Support OOS investigations, deviations, and non-routine testing activities.
• Calibrate and maintain analytical instrumentation.
• Review and verify analytical data and results.
• Prepare technical reports and communicate results to QA, Production, and other stakeholders.
• Maintain GMP, GLP, safety, and documentation standards.

Requirements

• Scientific qualification (minimum A-Level, HNC, or equivalent).
• Previous laboratory experience in industry or academia.
• Genuine interest in chemistry and laboratory-based work.
• Understanding of GMP, GLP, and quality-focused working practices.
• Strong attention to detail and ability to follow SOPs accurately.
• Excellent communication and organisational skills.
• Ability to work independently and as part of a collaborative team.

Desirable Experience

• Pharmaceutical, biotechnology, QC, QA, R&D, or development environments.
• Hands-on experience with HPLC or other analytical techniques.
• Stability testing and analytical investigations.

Important Note

This site manufactures antibiotic products. Applicants must not have a penicillin allergy and will be required to disclose any relevant medical conditions during the application process.