Quality Control Analyst

Kenton Black; Liverpool; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading pharmaceutical manufacturer in Liverpool is seeking a QC Analyst to ensure the safety and compliance of products through rigorous testing. The ideal candidate will have a relevant degree and experience in a GMP-regulated lab, with opportunities for professional development and career growth.

Qualifications

• 1–3 years of experience in a GMP-regulated pharmaceutical laboratory.
• Proficiency in HPLC; experience with other analytical chemistry techniques is advantageous.
• Familiarity with regulatory guidelines (MHRA, FDA, ICH) is a plus.

Responsibilities

• Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.
• Operate and maintain analytical instruments including HPLC, GC, ICP.
• Ensure strict adherence to cGMP and internal quality standards.

Skills

Attention to detail

Analytical techniques

Independent work

Education

BSc in Chemistry

BSc in Pharmaceutical Sciences

Tools

HPLC

GC

ICP

Job description

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Head of Sector - Pharmaceuticals and CROs at Kenton Black

Our client is a well-established, sterile GMP-accredited pharmaceutical manufacturer based in Liverpool, known for producing high-quality pharmaceutical products for both UK and international markets, exporting products to over 20 countries worldwide.

Are you a skilled QC Analyst with a passion for pharmaceutical quality and compliance? Do you thrive in a GMP-regulated environment and enjoy working with advanced analytical techniques? If so, we want to hear from you!

QC Analyst

Liverpool

As a QC Analyst, you will play a key role in ensuring the safety, efficacy, and compliance of pharmaceutical products through rigorous analytical testing.

The responsibilities of the QC Analyst include:

1. Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.
2. Operate and maintain analytical instruments including HPLC, GC, ICP, wet chemistry, and titrations.
3. Assist in the introduction and validation of new methods and equipment.
4. Assist laboratory and technical managers as a technical specialist providing advice and technical detail for routine analysis.
5. Perform equipment calibration and ensure accurate documentation.
6. Assist in the investigation and documentation of Out of Specification (OOS) and Out of Trend (OOT) results.
7. Ensure strict adherence to cGMP and internal quality standards.
8. Compile, interpret, and report analytical data for R&D and regulatory purposes.

The ideal candidate for the QC Analyst position will have:

1. BSc (or higher) in Chemistry, Pharmaceutical Sciences, or a related discipline.
2. 1–3 years of experience in a GMP-regulated pharmaceutical laboratory.
3. Proficiency in HPLC; experience with other analytical chemistry techniques is advantageous.
4. Strong attention to detail and ability to work independently.
5. Familiarity with regulatory guidelines (MHRA, FDA, ICH) is a plus.

In return, you’ll join a supportive team with opportunities for professional development, ongoing training, and career progression within a growing pharmaceutical business.

Seniority level

• Associate

Employment type

• Full-time

Job function

• Science and Research

Industries

• Pharmaceutical Manufacturing