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This role involves leading the development and delivery of strategic life sciences partnerships for the South West Secure Data Environment (SWSDE). Responsibilities include building relationships with life science organizations, developing commercial models, and ensuring governance and ethical standards are maintained.
The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include coordinating inspection readiness, supporting compliance activities, and implementing global quality initiatives. The role requires strong knowledge of pharmaceutical regulations and quality systems, with a focus on collaboration and process improvement.
This role involves managing and improving quality systems across CSL's European and global affiliates, ensuring compliance with regulatory requirements and CSL standards. Responsibilities include coordinating inspection readiness, maintaining quality KPIs, and supporting global quality initiatives.
This role involves managing and maintaining quality systems, ensuring compliance with regulatory requirements, and supporting inspection readiness across CSL's global affiliates. You will collaborate with various functions to implement quality initiatives and improve processes.
The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include inspection readiness, process harmonization, and supporting quality initiatives. The role requires collaboration with multiple functions and stakeholders, with a focus on compliance and continuous improvement.
The Quality Manager role involves maintaining and improving quality management systems, ensuring compliance with regulatory requirements, and supporting inspection readiness across CSL's global affiliates. You will collaborate with cross-functional teams, manage quality processes, and implement electronic quality systems.
A little outside Milton Keynes, but within reach.
This role involves leading a global team of clinical operations experts, driving the strategy for oncology clinical trials, and collaborating with key stakeholders to accelerate development timelines and improve health outcomes. The position requires extensive experience in clinical trial management and leadership.
As a Data Engineer in Autonomous Systems, you will work on the AutoLabs project, building the data platform that captures, stores, and serves high-frequency multimodal data from robotic systems, sensor rigs, and lab instruments. You will collaborate with AI researchers, software engineers, and domain scientists to create a robust data layer for autonomous operations, focusing on high-throughput, low-latency ingestion and data validation.
This role involves collaborating with scientists and engineers to build robust, reproducible data pipelines for diverse research projects. You will ensure datasets are accurate, version-controlled, and ready for machine learning, working hands-on with cutting-edge technologies and methodologies.
The Controlled Environment Lead will build and oversee plant growth and phenotyping facilities, ensuring controlled and reproducible environments for high-impact plant science research. Responsibilities include hands-on cultivation, data collection, and leading the team to support scientific and commercial goals.
This role involves managing the partnership and operational delivery of EIT's Oxford Clinic, including liaison with the clinical services partner, stakeholder communication, and financial oversight. The position focuses on building, launching, and growing innovative healthcare services.
This role involves leading the clinical development strategy for GSK's Hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific and clinical strategies, managing cross-functional teams, and ensuring regulatory compliance and market readiness for innovative oncology therapies.
This role involves designing and developing internal applications and web-based tools to support scientific research and drug discovery. You will work with JavaScript/TypeScript, React, .NET/C#, and Python, and collaborate closely with bioinformaticians, data scientists, and biologists.
This hands-on manufacturing role involves executing production processes in a GMP cleanroom environment, operating cell-processing equipment, and maintaining cleanroom standards. The role supports continuous improvement and quality assurance, with a focus on delivering autologous cell therapy products.
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