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.
The Data Solution Architect designs end-to-end data solutions, including data integration, warehousing, governance, and analytics. They work closely with technical leads and data teams to ensure scalable, secure, and governed solutions, influencing the data architecture of a rapidly evolving biotech company.
This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.
This role involves servicing, installing, repairing, and calibrating sophisticated diagnostic systems in pathology departments and NHS laboratories. You will support flow cytometry, cell separation, and diagnostics products, requiring a strong background in electronics or electro-mechanical service and excellent customer service skills.
This role involves servicing, installing, repairing, and calibrating sophisticated diagnostic systems in pathology departments and NHS laboratories. You will support flow cytometry, cell separation, and diagnostics products, requiring a strong background in electronics or electro-mechanical service and excellent customer service skills.
The BioAssay Scientist role involves performing a range of biological and analytical testing activities, including ELISA, cell-based assays, and Biacore assays. Responsibilities include maintaining GMP-compliant documentation, supporting laboratory operations, and building strong relationships with clients.
This role involves performing routine and non-routine testing of biologic drug substances, coordinating assay activities, managing project timelines, and ensuring GMP-compliant data. You will also support method development, validation, and troubleshooting, while mentoring colleagues and maintaining laboratory operations.
Operate and monitor manufacturing processes in a cGMP-regulated biopharmaceutical environment, supporting the production of life-changing medicines. Perform troubleshooting, contribute to process improvements using Lean methodologies, and assist in validation and documentation activities. Work within a rotating shift pattern in a safety-focused, highly regulated team setting.
This role involves developing and optimizing LC-MS workflows for single-cell proteomics and metabolomics, supporting researchers in experimental design and data interpretation, and collaborating with multidisciplinary teams to advance cutting-edge mass spectrometry techniques. The position is ideal for a scientist who enjoys method development, troubleshooting, and translating advanced MS technologies into high-impact research.
This role involves conducting high-impact research in plant specialised metabolism engineering, focusing on the development of novel decarbonised plant-based production of food and medicines. The scientist will work in a collaborative environment, designing and conducting experiments, developing customized libraries, and driving the translation of research into real-world solutions.
This role involves designing and prototyping generative machine learning models for protein design, with a focus on real-world biological functionality. The scientist will build scalable data pipelines, optimize model performance, and collaborate closely with biologists to test predictions in wet lab environments. A strong research background and passion for interdisciplinary innovation are essential.
This role involves developing, validating, and executing ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in a regulated GcLP environment, manage critical reagent characterization, and contribute to clinical sample testing using Watson LIMS. The position emphasizes scientific rigor, regulatory compliance, and collaboration within a high-performance team advancing novel bioanalytical assays.
This PhD project focuses on understanding the genetic mechanisms behind sexually antagonistic selection in fruit flies. You will use bioinformatics, genome engineering, and advanced sequencing techniques to identify and validate sexually antagonistic genes, explore their effects on fitness, and uncover the molecular mechanisms of sexual conflict. The role offers interdisciplinary training and collaboration opportunities within the Norwich Research Park.
Develops and validates ligand-binding and cell-based assays to support clinical programs for mRNA medicines. Performs pharmacodynamic and immunogenicity testing in compliance with GcLP, using platforms like Thermo Watson LIMS. Contributes to assay development, reagent management, and regulatory documentation in a fast-paced, innovative lab environment.
