Job Description

?QC Analyst - Pharmaceuticals
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.

Skills Required