QC Analyst – Pharmaceuticals

Location: New Malden

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