support the delivery of R&D programs at Gilead. EXAMPLE RESPONSIBILITIES: Design and implement protein engineering workflows to support antibody-based therapeutic discovery Implement molecularbiology cloning strategies, recombinant protein expression (mammalian), purification (AKTA), and characterisation (HPLC, DLS, DSF), including affinity determination (SPR and BLI) Generate, analyse, and … analytical abilities with high attention-to-detail as demonstrated through publications, past experiences and/or academic achievements Experience in using sequence analysis/molecularbiology software, protein expression, purification, and biophysical characterisation Desirable experience in molecular modelling, and the use of protein modelling and design software more »
fields. Support the development of biomarker assays in the laboratories, where appropriate. Requirements Academic qualification in a biological discipline with a good understanding of molecularbiology and transcriptomics (RNA sequencing and RT-qPCR), and their application to biomarker analysis in clinical studies. Practical experience of the complete workflow … for RNA sequencing experiments, including sample extraction, library preparation, quality control, sequencing runs, and troubleshooting. Experience in MolecularBiology methods, including RNA extraction from various biofluids and tissue matrices, primer and probe design, quantitative PCR (real-time and/or ddPCR) and data analysis. Experience of working with more »
and a commercial presence in many global locations across the US, APAC and Europe. Oxford Nanopore employs from multiple subject areas including nanopore science, molecularbiology and applications, informatics, engineering, electronics, manufacturing and commercialisation. The management team, led by CEO Dr Gordon Sanghera, has a track record of more »
Contribute to the development and training of project teams in regulatory affairs. Qualifications/Experience required: * Bachelor's degree in a science subject (e.g., molecularbiology, biomedical sciences) * Two or more years of experience in regulatory affairs within the diagnostics or medical devices industry * Strong knowledge of FDA more »
