Latest UK roles, updated daily.
This role involves leading communications and strategy initiatives to support R&D priorities in the Office of the Chief Scientific Officer. You will collaborate with senior leaders, develop clear scientific narratives, and ensure effective communication to diverse stakeholders.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, working with cross-functional teams to define the strategic vision and operational plan. Key responsibilities include managing the development team, ensuring regulatory approval, and aligning with GSK's oncology strategy.
This role involves designing, prototyping, and characterising MEMS devices for next-generation nanopore sequencing technologies. The Senior MEMS Development Engineer will work closely with a multidisciplinary team to develop novel microfabricated devices, tackle microfabrication challenges, and collaborate with external partners.
This role involves leading the development of innovative metabolic engineering and synthetic biology approaches to optimize plant respiratory activity, energy status, and redox balance. The scientist will design and implement engineering strategies, conduct experiments in plant cell cultures and whole plants, and collaborate with multidisciplinary teams to translate research into real-world solutions.
This role involves servicing, installing, repairing, and calibrating sophisticated scientific and laboratory systems used in pharmaceutical and research environments. You will work with high-value capital equipment and receive full product training.
This role involves servicing, installing, repairing, and calibrating sophisticated scientific and laboratory systems used in pharmaceutical and research environments. The position requires a background in field service engineering and a qualification in electronics, with experience in high-value capital equipment.
This role involves providing engineering support for GMP manufacturing equipment, ensuring operability and reliability across process platforms. Responsibilities include troubleshooting, authoring technical documents, and leading small-to-medium sized projects. The position is hands-on and cross-functional, essential for mRNA manufacturing success.
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 leading the scientific evaluation and application of foundation models in drug development and translational research. The individual will act as a key collaborator to research, product, and business teams, translating advanced biology and machine learning into practical customer solutions. Mentoring junior scientists and contributing to real-world discovery workflows are central to the position.
This undergraduate placement offers hands-on experience within Pfizer’s Global Hospital & Biosimilars Commercial team, focusing on portfolio management, supply chain dynamics, and data-driven commercial strategies in the NHS environment. You’ll support performance tracking, manage supply shortage communications, and contribute to project implementation while gaining cross-functional exposure. The role emphasizes analytical development, stakeholder engagement, and commercial acumen in a patient-centric healthcare setting.
This role involves hands-on maintenance and troubleshooting of GMP and non-GMP equipment in a new manufacturing facility. Responsibilities include equipment reliability, CMMS ownership, and collaboration with Engineering and QA on capital and reliability initiatives.
Manages project installations across business areas, ensuring timely delivery and clear communication with clients and internal stakeholders. Coordinates implementation meetings, maintains project documentation, and tracks equipment delivery timelines. Requires strong organisational skills and adherence to project plans.
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 planning and executing high-quality medical and scientific engagement activities such as advisory boards, congress symposia, standalone meetings, and medical education programs across key therapeutic areas including Oncology, Cardiovascular Disease, and Neuroscience. The position ensures operational excellence by translating scientific strategies into actionable plans, managing cross-functional collaboration, and maintaining compliance with standardized processes. It plays a central role in improving workflows, vendor coordination, and continuous improvement within international medical affairs.
This role involves leading pharmacovigilance and safety science activities across Roche’s medicine portfolio, with responsibilities spanning signal detection, risk management, and safety reporting. The individual will contribute to clinical development strategies, oversee post-market safety assessments, and ensure compliance with global regulatory standards. Working within a hybrid model in Welwyn, the position requires strong scientific analysis, leadership, and cross-functional collaboration in a regulated environment.
