Biotechnology Jobs

• Oxford
• On-site
• Senior · manages people
• Permanent

Lead a flagship plant biotechnology research programme focused on photosynthesis, carbon assimilation and nitrogen fixation to boost crop yields and cut inputs. You will coach and oversee Group Leaders, run your own independent research, recruit scientists and postdocs, and drive stage-gated projects toward commercial and IP impact within a rapidly scaling institute.

• Oxford
• On-site
• Permanent

Establish an automated, image-based phenotypic screening platform for plant cells, designing high-throughput assays and fluorescence reporter systems. Build reproducible image acquisition and analysis pipelines covering segmentation, feature extraction and phenotypic classification, working with automation and AI teams on scalable workflows.

High-Content Imaging · Confocal Microscopy · CRISPR

• London
• On-site

Contributes to the design, execution, analysis and reporting of hepatology clinical studies across all development phases, working with clinical operations, biostatistics, data management and regulatory affairs. Reviews safety, efficacy, biomarker and PK/PD data, supports protocol and CSR development, and engages with investigators and sites. Based on-site in London or Waltham, MA.

• London
• Hybrid
• PLN 228,000 – PLN 380,000 pa

Designs disease data information models for priority discovery areas, writing mapping rules to harmonise biomedical data and building quality checks that keep models trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams to get models adopted.

NCI Thesaurus · MONDO · EFO +6

• London
• Hybrid · 3 days in office
• Lead

Lead medicinal chemistry strategy across drug discovery programmes, from hit identification through lead optimisation to candidate nomination, while working hands-on as an individual contributor. Partner closely with AI/ML platform teams to shape predictive models, manage CRO resources and KPIs, and represent the company externally with collaborators.

AlphaFold

• London
• Hybrid · 3 days in office
• Senior

Lead the hardening and scaling of an inference platform serving fleets of cutting-edge ML models for scientific applications. Set strategy and roadmaps, architect next-generation services to solve scaling limits, and partner with research, product and operations teams to align infrastructure with biotech R&D cycles.

Kubernetes · Google Cloud Platform · NVIDIA GPU +1

• Reading
• Hybrid
• Mid-level

Supports clinical trials by designing, setting up and maintaining Interactive Response Technology (IRT) solutions, translating supply requirements into system specifications. Contributes to risk assessments, user acceptance testing and validation documentation, and advises study teams on IRT processes. Works with cross-functional global stakeholders on study startup, amendments and continuous improvement.

IRT · RTSM · IVRS +1

• Livingston
• On-site
• Entry level

Assembles clinical trial test kits with specimen collection materials according to protocol, prepares investigator instruction manuals and flowcharts, and packages completed kits with documentation and ancillary supplies for shipment. Monitors inventory levels and alerts supervisors when supplies run low to prevent study delays. Site-based role requiring strong attention to detail and organizational skills.

• Norwich
• £21,805 pa
• Entry level
• Contract

A four-year PhD project using engineering biology to develop bacterial and human ferritin nanocages for encapsulating small molecules, peptides and proteins, with applications in biocatalysis and therapeutics. The work spans protein purification, bioanalytical methods, spectroscopy, mass spectrometry and microscopy, targeting enzymes such as hydrogenase and targeted molecular delivery. Based in the Le Brun lab at UEA's School of Chemistry, Pharmacy and Pharmacology.

Ferritin

• Macclesfield
• On-site
• Permanent

Perform structural elucidation and impurity characterisation of small molecule APIs using advanced mass spectrometry, supporting regulatory submissions and control strategies. Develop Eurofins' MS capabilities, collaborate with cross-functional teams, and work to GLP, cGMP and SHE standards at a client pharmaceutical facility.

• United Kingdom
• Remote
• Lead

Supports central comparator sourcing for clinical trials on a client-dedicated FSP team, covering market intelligence, sourcing recommendations, and purchase order execution across EMEA. Acts as an SME on the external comparator landscape, advising on regional and central/local sourcing strategy while escalating quality or temperature issues to the client.

• Exeter
• Entry level
• Contract

A cross-institutional PhD studentship analysing whole genome sequencing data from millions of individuals across UK Biobank, All of Us and Our Future Health to identify rare causal variants for musculoskeletal disorders, then functionally validating them in human cell and tissue models using CRISPR-Cas9, transcriptomics and cellular phenotyping. Split between computational genomics at Exeter and laboratory work at Oxford, it develops a dual skill set in statistical genetics and experimental validation.

UK Biobank · All of Us · Our Future Health +4

• Belfast
• £50,000 – £60,000 pa
• Lead · manages people

Leads a Clinical Method Development and Validation team, overseeing bioanalytical method delivery for a New Product Development programme. Provides technical leadership in a GLP-compliant lab, acting as expert in extraction techniques and optimising HPLC, UPLC and LCMSMS systems while mentoring the team.

HPLC · UPLC · LCMSMS +1

• London
• Hybrid
• Permanent

Architect novel generative models to design functional proteins, working in an interdisciplinary team of ML researchers, protein engineers and biologists. Split roughly 90% model building and 10% self-development, spanning data curation, evaluation metrics, prototyping, cloud training/inference and wet lab testing campaigns.

• Uxbridge
• Director

Serves as primary medical accountability for Phase 1–3 clinical trials in neuroscience, leading medical monitoring, safety assessment and benefit/risk analysis within a matrixed study delivery team. Partners with clinical scientists on protocol design, site interactions and health authority submissions, and builds relationships with principal investigators and thought leaders.