Quality Control Analyst

JR United Kingdom; Birkenhead; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading pharmaceutical manufacturer seeks a QC Analyst to ensure the safety and compliance of products through analytical testing. The role offers an opportunity to work in a GMP-regulated environment, performing routine testing and maintenance of advanced analytical equipment, contributing to product quality and regulatory compliance.

Benefits

Professional development

Ongoing training

Career progression opportunities

Qualifications

• 1-3 years in a GMP-regulated pharmaceutical lab.
• Proficient in HPLC; other analytical methods advantageous.
• Familiar with regulatory guidelines (MHRA, FDA, ICH) is a plus.

Responsibilities

• Conduct routine and non-routine testing of raw materials and finished products.
• Operate and maintain analytical instruments.
• Assist in validation of new methods and equipment.

Skills

Attention to Detail

Analytical Techniques

GMP Compliance

Education

BSc in Chemistry

BSc in Pharmaceutical Sciences

Tools

HPLC

GC

ICP

Job description

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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:

• Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.

• Operate and maintain analytical instruments including HPLC, GC, ICP, wet chemistry and titrations.

• Assist in the introduction and validation of new methods and equipment

• Assist laboratory manager and technical managers in the capacity as a technical specialist providing advice and technical detail for routine analysis

• Perform equipment calibration and ensure accurate documentation.

• Assist in the investigation and documentation of Out of Specification (OOS) and Out of Trend (OOT) results.

• Ensure strict adherence to cGMP and internal quality standards.

• Compile, interpret, and report analytical data for R&D and regulatory purposes.

The ideal candidate for the QC Analyst post will have:

• BSc (or higher) in Chemistry, Pharmaceutical Sciences, or a related discipline.

• 1–3 years of experience in a GMP-regulated pharmaceutical laboratory.

• Proficient in HPLC; experience with other analytical chemistry techniques is advantageous.

• Strong attention to detail and ability to work independently.

• 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.