Quality Control Analyst

Social network you want to login/join with: Quality Control Analyst, Warrington, Cheshire col-narrow-left Client: Location: Job Category: Other – EU work permit required: Yes col-narrow-right Job Views: 8 Posted: 07.06.2025 Expiry Date: 22.07.2025 col-wide Job Description: 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 and technical managers 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 role 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. #J-18808-Ljbffr