QC Analyst

Location: South London (Fully Site-Based)

Employment Type: Full-Time

About the Role

We are seeking a highly skilled and motivated Quality Control Analyst to join a pharmaceutical team in South London. This is a fully site-based role, ideal for someone with a strong background in analytical chemistry and a passion for maintaining high standards in a GMP-regulated environment.

Key Responsibilities

• Perform routine and non-routine analysis of raw materials and finished pharmaceutical products using HPLC (essential), GC, UV, and FTIR techniques (preferred).
• Demonstrate advanced troubleshooting skills with HPLC systems and lead Out of Specification (OOS) investigations.
• Ensure all testing is conducted in compliance with GMP standards and internal SOPs.
• Accurately document results and maintain laboratory records in accordance with regulatory requirements.
• Support method development and validation activities as needed.
• Collaborate with cross-functional teams to resolve quality issues and improve laboratory practices.

Requirements

• Proven experience in a GMP-compliant pharmaceutical QC laboratory.
• Strong proficiency in HPLC is essential, including troubleshooting and OOS investigations.
• Experience with GC, UV, and FTIR techniques is highly desirable.
• Excellent attention to detail and ability to work independently in a fast-paced environment.
• Strong communication and documentation skills.

What’s on Offer

• Competitive salary and benefits package.
• Opportunity to work in a dynamic and supportive team.
• Career development and training opportunities.

Key Words: QC, quality control, analyst, analytical scientist, chemistry, chemist, chromatography, HPLC, GC, TLC, FTIR, UV Vis, techniques, GMP, Good Manufacturing Practice, laboratory technician, pharmaceutical, healthcare, supplement, medical.

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