QC Analyst

Research Quality Association (RQA); Greater London; On-site; GBP 80,000 - 100,000; Full time

Job summary

A leading pharmaceuticals organization is seeking a QC Analyst in South London. This fully site-based role requires a strong background in analytical chemistry and proficiency in HPLC. You will conduct routine analyses, ensure GMP compliance, and document results accurately. The position offers a competitive salary and benefits, along with opportunities for career development within a supportive team.

Benefits

Competitive salary

Career development opportunities

Supportive team environment

Qualifications

• Experience in a GMP-compliant pharmaceutical QC laboratory.
• Exceptional proficiency in HPLC required.
• Experience with other analytical techniques preferred.
• Excellent attention to detail and ability to work independently.

Responsibilities

• Conduct analysis of raw materials and finished products.
• Lead OOS investigations.
• Ensure compliance with GMP standards.
• Document results and maintain laboratory records.
• Support method development and validation activities.

Skills

Proficiency in HPLC

Troubleshooting skills

Attention to detail

Communication skills

FTIR

Attention to Detail

Tools

HPLC

GC

FTIR

UV

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.