The Role We are looking for an Analytical Scientist to join our team in Alnwick on a 12-month fixed-term contract to cover maternity leave. In this role, you will develop, validate, and apply analytical methodologies within a regulated environment, ensuring full compliance with GLP/GMP guidelines. You will also provide expert advice and problem-solving for specialized analytical techniques.Main tasks and responsibilities Analysis of drug substances, raw materials, intermediates and drug products using a variety of analytical techniques. Develop, validate and report analytical methodology and, where appropriate, provide resolution to technical problems Apply analytical methodologies during the quality control and stability evaluation of a range of materials Prepare work protocols for approval, critically assess data generated and review data from peers Prepare and review reports, quality documents and training documentation Acquire/record data in a manner that complies with GxP and internal policies/procedures Perform assigned roles within Quality Control such as equipment responsible operator, training, equipment hardware and/or software validation and the ordering of consumable items Work with due regard to health and safety of self and others Work flexibly across the site to meet business needs - meaning adapting to changing priorities and tasks, not physical mobility or changes to working hours. We welcome different working needs and are happy to discuss any adjustments required. Qualifications and experience required BSc (Hons) or equivalent in a relevant scientific discipline. Experience in the application of analytical methodologies in a pharmaceutical environment is advantageous. Ability to communicate effectively in a way that supports collaboration. The ability to critically assess data and have a flexible approach to new work challenges Competent in the use of Microsoft Office packages such as Word and Excel.