Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for aAnalytical Associate in Analytical Development for Synthetic MoleculesBackground:Pharma Technical Development (PTD) is a global team of over 2,000 experts focused on developing innovative medicines to address patients' needs.Within PTD, Synthetic Molecules Technical Development (PTDC) specializes in drug substance, drug product, and analytical sciences. PTDC is instrumental in advancing the synthetic molecules pipeline, supporting research, early development, and clinical trials through technical innovation and collaboration.This opportunity lies within analytical development for synthetic molecules, where cutting-edge techniques like high-performance liquid chromatography, gas chromatography, ion chromatography and mass spectrometry are employed to develop efficient and robust analytical methods. The goal is to ensure the release of clinical trial products and their eventual commercial supply through a strong control strategy.Tasks & Responsibilities:Development, improvement and validation of analytical methods for the quality assessment of starting materials, intermediates, reaction monitoring, active substances and galenical forms.Thorough and efficient planning, execution and documentation of experiments in collaboration with the relevant team members, analytical project lead and your supervisor, following current GxP guidelines as well as the relevant SOP’s.Work on end to end processes in close collaboration with other associates, scientists, and partners from other departments to ensure efficient analytics and continuous improvement.Coordination of analytical activities including sample management for the development of synthetic products.Authoring of documents, e.g. analytical procedures, and validation reports.Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases.Must Haves:You hold a solid vocational qualification with at least 1-3 years’ experience in the pharmaceutical industry with a strong focus on analytical methods development (i.e. chromatography) or a bachelor's degree (Analytical Chemistry, Biochemistry, Biotechnology or related field) Hands-on experience in analytical instrumentation and techniques (e.g. HPLC, GC, KF)Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phasesExcellent command of English. Good command of German would be a plusA strong interest / background in analytical methods developmentA good scientific writing style and good documentation practice for utilization of corresponding data in regulatory filingsExcellent digital skills and innovative mindsetPreparedness to learn, continuously improve and apply novel ideas, tools and processes to quickly adapt to a fast changing environmentSelf-motivated, open-minded, proactive, reliable, goal-oriented and an excellent team playerA strong quality mindset and excellent attention to detailWhat you will be offered:An opportunity to work in one of the world's most important pharmaceutical companiesModern campus with plenty of green spaces and meeting areasCentral location in BaselVaried job profileFurther training opportunities through temptrainingWorking in a dynamic and motivated teamIf you are interested please send your application documents addressed to Ms Diana Afonso.Basel-Stadt Aargau Solothurn Pharma Analytics Development Quality Control Validation Documentation GMP GxP Process Improvement j4id9916476a j4it1043a j4iy25a