Biotechnology Jobs

• Oxford
• On-site
• Mid-level
• Permanent

Designs and runs evolution campaigns and selection schemes to optimise photosynthetic proteins, applying genome editing, directed evolution and protein engineering within a stage-gated plant engineering programme. Works in an interdisciplinary team translating photosynthesis, carbon fixation and yield findings into commercial and IP opportunities.

• Oxford
• On-site
• Mid-level
• Permanent

Designs and runs quantitative genetics experiments to assess polygenic traits in field environments, managing multi-location field sites and identifying germplasm for trait variation analysis. Works within the Photosynthesis and Yield programme, taking a plants-down approach to build discovery pipelines from natural variation and evolutionary signals, with scope to contribute to publications, IP and commercial translation.

• 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

• Warsaw, Poland
• 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 to keep it trustworthy. Works hands-on in code and modelling tools, using AI assistants daily, and partners with research, ontology and data platform teams plus external partners.

NCI Thesaurus · MONDO · EFO +6

• London
• £47,500 pa
• Entry level
• Contract

Lead a computational project studying how driver mutation clones interact with their microenvironment in chronic liver disease and liver cancer. Develop graph neural networks, transformers and generative AI methods on large-scale spatial genomics, single-cell and imaging data, embedded across the Crick and Wellcome Sanger Institute with joint supervision.

PyTorch · JAX · NumPy +2

• Ongar
• On-site
• Mid-level
• Permanent

Develops and validates reverse-phase and chiral HPLC methods for characterising radio-labelled APIs, troubleshooting instrumentation and methods, and ensuring results meet written procedures and client timelines. Leads out-of-specification investigations and quality records, represents the analytical team in customer meetings, and mentors junior scientists across multiple concurrent projects.

HPLC

• London
• On-site
• Junior

Work in the hardware team developing mechanical solutions for lab automation systems, refining existing designs and part sourcing, and assembling, testing and validating complex devices. Collaborate across disciplines in an Imperial College innovation hub lab, incorporating user goals into product design. Requires a mechanical engineering background and CAD experience, ideally Solidworks.

SolidWorks

• Cambridge, United States
• Hybrid · 3 days in office
• Lead

Lead DMPK strategy across drug discovery projects, designing screening cascades and mechanistic experiments while integrating DMPK, PD and toxicology data for dose and safety predictions. Work closely with AI/ML platform teams to optimise computational ADME models and author regulatory sections, in a hybrid Cambridge, MA role.

Python · R

• Cambridge, United States
• Hybrid · 3 days in office
• Lead

Lead the safety assessment strategy for small molecule and biologic drug discovery projects from inception to regulatory submission, designing screening cascades and mechanistic experiments. Partner with machine learning researchers to build predictive toxicology models and manage CRO relationships for outsourced wet-lab data generation, while mentoring junior team members.

KNIME · Python

• London
• Hybrid
• Senior
• Permanent

Leads global pharmacovigilance operations, overseeing case intake, ICSR processing and regulatory reporting across clinical and post-marketing portfolios. Acts as business administrator for the Veeva Safety database and primary interface with PV vendors, while driving SOPs, inspection readiness and safety data exchange agreements.

Veeva Safety

• Uxbridge
• Director

Serves as primary medical accountability for multiple Phase 1-3 clinical trials in GI oncology, leading medical data review, safety assessment and site interactions within a Study Delivery Team. Partners with Clinical Scientists on protocol design, benefit/risk analysis and health authority interactions, while building relationships with principal investigators and thought leaders.

• London
• Hybrid
• Director
• Permanent

Safety expert serving as global PV lead for gene therapy products across investigational and marketed phases, owning benefit-risk strategy, aggregate reports (PSURs, DSURs) and risk management plans. Also acts as medical monitor, providing clinical oversight, real-time AE/SAE review and signal detection in close collaboration with cross-functional teams and health authorities.

Veeva

• 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.

• London
• Director · manages people
• Permanent

Lead the team behind hybrid on-prem and cloud compute infrastructure, Kubernetes clusters, and scientific compute environments supporting ML and drug discovery. Own platform strategy, CI/CD maturity, observability, and security controls for sensitive patient-derived data, reporting to the VP of Engineering.

Kubernetes · Kubeflow · GPU Compute +3

• Warrington
• On-site
• Senior
• Permanent

Contributes to manufacturing sciences by ensuring manufacturing quality, process validation and regulatory compliance for biopharmaceutical and diagnostic products. Develops and implements CMC strategies, standardises procedures and drives process improvements, while mentoring technical staff and leading cross-functional teams in a regulated GMP environment.

FDA · EMA