About you As a Technical Expert you will have accountability for leading, managing and driving the TQA promise, you will demonstrate your expertise across technical areas and have the confidence to provide support and guidance on specific techniques to both Colleagues and Clients. Required skills and experience: BSc / MSc/ PhD in Biochemistry/Chemistry (or related scientific discipline) is essential. Education and work-related experience required with at least 5 years direct experience analytical development, preferably in a pharmaceutical/biotech industry setting. LC-MS, including high-resolution accurate mass analysis for elucidation of intact mass, protein/peptide sequencing, PTMs including oxidation, deamidation or glycosylation and disulphide bridge mapping. Can recognise the positive and negative impacts of utilising particular methods with a view to providing the best solution to the Client. Ensuring that all processes are aligned to the needs of the Client and fit with the schedule of works. Strong experience of creating mass spectrometry, chromatography and sample preparation methods. Solutions-focused with the ability to independently troubleshoot and source solutions, convey these to both Clients and members of the business in a methodical and simplistic way. Clear written and verbal communications skills with the ability to clearly convey processes, results and key messages and able to build rapport, quickly and effectively. About the opportunity Key activities: Provide technical expertise within the LCMS characterisation team, responsible for design of study and the scientific integrity of multiple analytical projects undertaken by the laboratory. Provide strategic direction to ensure our services remain the best possible solutions for our clients within the biopharmaceutical industry. Lead on R&D activities within the LCMS Characterisation team producing research material for publication and presentation at industry events. Author and/or critically review analytical project reports in a speedy and efficient manner regarding accurate interpretation of the data and compliance with the Analytical Project Plan Ensure that all Quality Management documentation is completed in a timely manner Assist the Laboratory Manager in establishing Development Training plans for all team members In conjunction with the Project Manager and Laboratory Manager plan and organise analytical workload for themselves and other members of staff for whom they provide supervision, based upon business priorities and specific project deliverables Carry out project team briefings at the start of each project to explain the context of the project, define the deliverables and explain any specific testing requirements Carry out Team De-briefings (review) with team members at the end of each project to discuss best practice and learnings which could be applied to future projects Liaise with the Quality Group to advise of any atypical project timelines or requirements Communicate effectively with staff at all levels; regularly with Laboratory Managers, Project Managers and clients where applicable, providing detailed project status updates What we offer Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world. Competitive salary/benefits Development and career opportunities around the Globe Working in a highly motivated team and dynamic working environment We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin. Intertek operates a preferred supplier arrangement and we do not accept unsolicited approaches from agencies. ADZN1_UKTJ