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 documention 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