Method Validation Chemist

Method Validation Chemist As a Method Validation Chemist, you will be responsible for developing, validating and transferring analytical methods used to support pharmaceutical products and raw materials. Working within a GMP-regulated laboratory, you will play a key role in ensuring analytical methods meet regulatory standards and support quality control and product release. Key Responsibilities Develop and validate analytical methods in accordance with ICH and GMP guidelines Perform validation studies including accuracy, precision, specificity, linearity, range and robustness Support method transfer between laboratories where required Analyse pharmaceutical samples using techniques such as HPLC, GC, UV and dissolution Prepare validation protocols, reports and supporting documentation Investigate analytical deviations and contribute to continuous improvement activities Collaborate with Quality Control, R&D and manufacturing teams to support product lifecycle activities Requirements Degree (or equivalent) in Chemistry, Pharmaceutical Science, or a related scientific discipline Experience working in a GMP-regulated pharmaceutical laboratory Practical experience in analytical method validation Hands-on experience with techniques such as HPLC, GC or other chromatographic methods Strong understanding of ICH Q2 and pharmaceutical regulatory expectations Excellent attention to detail and strong documentation skills What’s on Offer Competitive salary depending on experience Opportunity to join a well-established pharmaceutical organisation Supportive and collaborative laboratory environment Career development opportunities within a growing company 📩 Apply now or contact CY Partners for more information on this exciting opportunity within the Tyne–Tees pharmaceutical sector. CY Partners – Talent for Science & Engineering Technologies