Biomedical jobs in Oxford

You will be closely engaged in all aspects of editorial work at Cell Press. Cell Press is an international organization with primary offices in Cambridge, Massachusetts; London; Amsterdam; and Beijing. This is a full-time editorial position, and we have a preference for candidates located near our Amsterdam NL or our London or Oxford UK offices.

You will focus on a range of innovative near-patient testing solutions. Working closely with the Sales Manager and Director of Business Development, you will receive structured product and sales training to help you confidently present technical features to NHS stakeholders.

About Princeton Biopartners: Princeton Biopartners is a leading provider of integrated consulting solutions to the life sciences sector. Our mission is to improve the evidence base, accessibility, and dissemination of biomedical innovations through strategic advisory, software development, and venture funding. We partner with leading pharmaceutical, biotechnology, and healthcare organizations to...

You will play a hands-on role in the development, optimisation, and validation of the Pictura Bio assay.

You will be expected to generate high-quality experimental data, document work rigorously, and contribute to assay robustness, reproducibility, and performance verification.

You must be available to work from Monday to Friday and willing to travel.

You must be legally working in United Kingdom.

Company Description LBG Medical is a trusted European manufacturer with over 45 years of experience, specialising in custom-made orthotics. The company is dedicated to advancing the field of foot care through its innovative Bio range of medical-grade prefabricated orthotics. By combining decades of expertise with leading advancements, LBG Medical delivers superior comfort, support, and clinical...

Job Title: Associate Product / Clinical Marketing Manager (Oncology Diagnostics) Status: Full Time Division: Commercial / Marketing Location: London-based (hybrid), remote (EU) considered for exceptional candidates Travel: Ability to travel up to ~25% of the time (primarily for conferences, partner meetings, and launch-related activities) Salary: Competitive Reporting: CEO, with structured,...

About OrganoX: OrganOx is an innovative, fast-paced, global medical device company with a mission to save lives by making every donated organ count. We are a commercial stage organ technology company, spun out of the University of Oxford in 2008, committed to improving transplantation outcomes throughout the world. The company's first product, the OrganOx Position Summary We are seeking a...

Senior Systems & Regulatory Software Engineer Medical Devices | High Salary or High-Rate Contract | Kent | Remote We are seeking an experienced Technical Expert to join our global team, working with active medical devices under MDR 2017/745 and ISO 13485 standards Electrionics device and audit experience is recognised. This is a fully remote role, offering the flexibility to work from...

You must have the right to work permanently in the UK with a willingness to travel as necessary.

You will live in, or within easy commuting distance of, Oxford. - During peak periods, some longer hours may be required and some working across multiple time zones due to the global nature of the programme.

One of our renown clients is seeking a driven and detail-oriented Genetic Engineer to join a leading biotechnology and life sciences organization. This is a hands-on research and development role focusing on genome editing, gene therapy, and molecular diagnostics using technologies such as CRISPR/Cas9, TALENs, and RNA-guided DNA modification. The successful candidate will be responsible for...

You will work on advanced brain-machine interfaces and non-invasive stimulation systems, integrating real-time behavioural and brain activity monitoring to deliver closed-loop interventions.

You will hold a PhD in biomedical engineering, neuroscience, or a related field, and have a strong track record in human neurophysiology, experimental medicine, or interactive systems.

We are seeking a full-time PA and Research Group Administrator to provide high-level administrative and secretarial support to the CHI lab at the Institute of Biomedical Engineering (IBME). This role will primarily support the Professor of Clinical Machine Learning, Professor David Clifton, as well as other academic members of the group. The position is permanent and full-time, although...

You will execute projects that combine strategic insight with tech-forward solutions to deliver end-to-end, decision-ready outputs for clients. The role requires intellectual curiosity, analytical rigor, creativity, and structured strategic thinking, with strong client engagement and clear opportunities for professional growth as a trusted extension of client teams.

You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use.

You will work closely with assay development, data science, regulatory, and external clinical partners.

You will play a hands-on role in the development, optimisation, and validation of the Pictura Bio assay.

You will be expected to generate high-quality experimental data, document work rigorously, and contribute to assay robustness, reproducibility, and performance verification.

You will play a hands-on role in the development, optimisation, and validation of the Pictura Bio assay.

You will be expected to generate high-quality experimental data, document work rigorously, and contribute to assay robustness, reproducibility, and performance verification.

You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use.

You will work closely with assay development, data science, regulatory, and external clinical partners.

You will play a hands-on role in the development, optimisation, and validation of the Pictura Bio assay.

You will be expected to generate high-quality experimental data, document work rigorously, and contribute to assay robustness, reproducibility, and performance verification.

You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use.

You will work closely with assay development, data science, regulatory, and external clinical partners.