Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.
Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.
A Research Scientist focused on applying Large Language Models to drug discovery, working in interdisciplinary teams to develop novel AI-driven approaches for biological and chemical challenges. The role involves advancing LLM techniques such as post-training, reasoning, tool-use, and alignment within a cutting-edge AI research environment. Collaboration with scientists and engineers is central to developing predictive models that accelerate rational drug design.
A Research Scientist in Machine Learning will develop novel deep learning models and algorithms to advance drug discovery at digital speed. Working in an interdisciplinary environment, they will apply cutting-edge ML techniques to complex biological and chemical problems, iterating closely with domain experts. The role involves leading high-ambition research projects, scaling training frameworks, and shaping the technical direction of AI-driven drug design.
This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based clinical development programmes. The scientist will lead assay development—including ADA, nAb, PK, and PD assays—using platforms like ELISA, MSD, and cell culture, while ensuring regulatory compliance and contributing to Moderna's expanding capabilities in Harwell. The position emphasizes collaboration across multidisciplinary teams and integration of digital and AI-enabled tools to enhance data interpretation and decision-making.
This role involves performing routine environmental monitoring, water sampling, and microbiological testing to support GMP quality control for mRNA products. The analyst will execute tests including sterility, bioburden, endotoxin, and TOC, while supporting method transfers, validations, and compliance with cGMP standards. The position requires strong documentation practices, collaboration with cross-functional teams, and active participation in quality systems such as investigations and audits.
This two-year graduate programme at GSK focuses on engineering and manufacturing, with rotations in various areas like project management, equipment reliability, and smart manufacturing. Participants will work on real-world challenges, apply digital and data analytics, and contribute to sustainability initiatives.
This industrial placement at GSK offers hands-on experience in chemistry-related roles, including Structural and Biophysical Sciences, Process Chemistry, and Analytical Development. You will work on real projects, gain technical skills, and collaborate with multidisciplinary teams, contributing to drug discovery and development.
This role involves designing and conducting molecular biology experiments within a plant science research programme focused on improving global food production and sustainability. The scientist will work on stage-gated research milestones, contribute to intellectual property and publications, and collaborate with cross-functional teams including AI, automation, and generative biology experts. Emphasis is placed on translating scientific discoveries into scalable, real-world commercial solutions with ethical and environmental considerations.
This role leads the molecular confirmation and genotyping of gene-edited and transgenic crop events, ensuring high-quality, data-rich handover to downstream teams. The candidate will establish stage-gate criteria, manage genotyping workflows across multiple technologies, and integrate with transformation, bioinformatics, and trait discovery teams. The position is central to building a scalable, industrial-grade pipeline for crop development in species such as corn and wheat.
This role involves leading health, safety, and biological compliance across a gene therapy organisation, with a focus on regulatory adherence, risk assessment, and biosafety oversight. The specialist acts as the appointed Biological Safety Officer, ensuring safe handling of biological materials and driving a strong safety culture through training and audits. Work includes developing safety systems, incident investigation, and maintaining compliance with UK legislation and internal standards.
Develops and optimizes metagenomic extraction and sequencing workflows for diverse sample types, focusing on low-biomass and inhibitor-rich matrices. Works end-to-end from DNA/RNA extraction to library prep, with emphasis on high molecular weight recovery and virology applications. Collaborates globally to enhance data quality and scalability for AI-driven biological discovery.
The Multi-Skilled Engineer II role involves maintaining and repairing pharmaceutical equipment and facility installations to support manufacturing and QC operations. Responsibilities include diagnosing and repairing equipment, conducting risk assessments, planning maintenance, managing critical spares, and providing support to other teams.
The role involves developing and characterizing molecular quantum materials for biomedical sensing, focusing on nanoparticle probes and their optical and spin properties. Responsibilities include preparing and testing nanoparticles, functionalizing surfaces, and collaborating with interdisciplinary teams to advance diagnostic methods.
This role involves managing clinical trials, including providing support on approval processes, trial management, recruitment strategies, and data quality. The position is part of the Tayside Clinical Trials Unit (TCTU) and focuses on both new and established drug and complex intervention trials, with a lead role in the BE-Genomics trial.
