The Role We are looking for an Analytical Scientist to join our team in Alnwick on permanent basis. In this role, you will develop, validate and apply analytical methodologies to support pharmaceutical development and manufacturing, while ensuring compliance with GLP/GMP guidelines. Key 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. Qualifications and experience required for competent performance BSc (Hons) or equivalent in a relevant scientific discipline. Experience in the application of analytical methodologies in a pharmaceutical environment is advantageous. Good written and oral communication skills 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. Eligibility to Work in the UK Please note that this position is not eligible for sponsorship under the UK points-based immigration system. If you require sponsorship, we will be unable to progress your application or make an offer of employment. As this is a permanent role, we are also unable to accept applications from candidates on a Graduate Visa.