Biotechnology Jobs

• London
• Mid-level

Mid-level individual contributor on GSK's Enterprise AI Forward Deployed Engineering team, embedded with business unit teams to prototype AI proofs of concept at a days-to-weeks cadence. Works under senior FDEs using AI coding assistants and multi-agent workflows as the default mode of building, then hands proven solutions off cleanly for productionisation.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• Barnard Castle
• On-site
• Senior

Lead and deliver Quality Assurance, New Product Introduction, validation and Computerised Systems Validation activities across projects and operations at a secondary manufacturing site. Plan, execute and document risk-based validation for processes, facilities, equipment and computerised systems, provide quality oversight for technical transfers and batch documentation, and support regulatory inspections. Works closely with project teams, engineering, IT and manufacturing.

MES

• Oxford
• On-site
• Senior
• Permanent

Designs and engineers plant specialised metabolism in cell cultures to produce high-value natural products for health and medicine, applying synthetic biology to optimise biosynthetic pathway flux and product tolerance. Works with AI and robotics teams on model-driven engineering and stage-gated milestones, with a focus on IP generation and translating research into commercial solutions.

• Oxford
• On-site
• Senior
• Permanent

Lead the development of a plant cell-based screening platform to evaluate carbon fixation, using quantitative methods and CRISPR-based genome editing in suspension cultures. Apply iterative design-build-test-learn cycles to identify improved photosynthesis enzyme variants and engineered pathways, advancing promising candidates into whole plants. Contribute to IP generation and collaborate across multidisciplinary teams.

CRISPR

• Cambridge, United States
• Hybrid · 3 days in office
• Senior · manages people

Experienced medicinal chemists lead portfolio drug discovery projects from initiation to clinical candidate selection, working as Project Lead or Medicinal Chemistry Lead. They partner closely with ML scientists to refine the AI drug design platform, manage CRO resources, and may line-manage teams of 2-4 chemists.

AlphaFold

• London
• Hybrid · 3 days in office
• Mid-level

Join the model performance and scaling team to implement and optimize LLM post-training methods on frontier models, working with JAX or PyTorch, parallelism strategies and GPU architectures. You will diagnose bottlenecks in distributed training and inference, deploy low-precision methods, and collaborate with research teams to turn new methods into production systems for drug design.

JAX · PyTorch · NCCL +5

• Uxbridge
• Hybrid
• Senior · manages people

Technical lead on assigned clinical studies, shaping SDTM strategies from protocol review through to global regulatory submission. Involves root cause analysis, cross-functional collaboration, data integration from CRF and non-CRF sources, and engagement with SDTM automation, metadata-driven processes and agentic AI workflows. Also provides quality oversight to team members and manages CRO and vendor programming activities.

Pinnacle 21

• London
• Hybrid
• Permanent

Customer-facing engineering role bridging frontier generative biology models and pharma/biotech clients. You own end-to-end deployments, building production-grade API integrations, data pipelines and model-serving infrastructure, often embedded on-site with partners, and feed customer insights back into product and research teams.

AWS · GCP · Azure +2

• Cambridge
• Director · manages people

Leads a team of medical writers and oversees strategic planning and drafting of complex regulatory submissions at the therapeutic area or portfolio level. Acts as subject matter expert, driving document strategy with cross-functional teams across Regulatory Affairs, Clinical Research and Clinical Data Science, plus process improvement and training initiatives.

Workday

• Cambridge
• Lead

Lead developability science across drug discovery programmes, designing and interpreting preformulation, solid-state and biopharmaceutic studies and integrating experimental, computational and AI-enabled approaches to guide candidate progression. Act as primary scientific client contact, lead projects from proposal to delivery, support business development and mentor junior scientists within a growing Cambridge team.

PBPK · DCS · Spray Drying +2

• London
• Hybrid
• Senior

Oversees quality control testing for a genetically edited cell therapy, acting as lead point of contact for external CDMOs and QC labs on GMP release, stability and method lifecycle work. Leads OOS/OOT investigations, reference standards and assay controls programmes, authoring and approving SOPs, COAs and protocols. Hybrid role based in London requiring close collaboration with contract test labs and management on compliance risks.

LIMS

• Uxbridge
• Director · manages people

Leads clinical strategy and execution for one or more GI oncology indications of a given asset, owning the Target Product Profile and disease area strategy. Manages a team of physicians and scientists designing, running, analysing and interpreting all clinical studies, and acts as internal and external clinical authority for regulatory interactions and business development. Requires deep therapeutic expertise and 8+ years of drug development experience, with international and domestic travel.

• Oxford
• Hybrid · 3–4 days in office
• Director

As an individual contributor in the Clinical Pharmacology group, you will develop quantitative strategies for dose selection, PK/PD characterization and regimen optimization across oncology, immunology and rare disease programs. You will partner with Pharmacometrics and QSP colleagues, represent CQP on program teams, and contribute to regulatory documentation and interactions.

R · Phoenix WinNonlin · NONMEM +2

• London
• On-site
• Lead · manages people
• Permanent

Owns the end-to-end sample-to-sequence pipeline for the Trillion Gene Atlas, spanning DNA extraction, library prep and sequencing dispatch across Phase 1 and Phase 2. Bridges R&D and production by scaling validated protocols, applying Lean/Six Sigma to improve throughput, and leading a small lab team while monitoring data return with bioinformatics partners.

Illumina · Ultima · PacBio +3

• Oxford
• On-site
• Entry level
• Temporary

Support assay development, qualification, validation and clinical sample testing within Moderna's Immunoassay group, generating bioanalytical data that informs clinical trials. Work is primarily lab-based (≥85% of time) under a study lead, with responsibility for data integrity, reagent preparation, equipment upkeep and compliance with GCP/ISO standards.

GraphPad Prism · LIMS · Word +2