Biotechnology Jobs in London

• London
• Hybrid · 3 days in office
• Senior

Research engineers translate frontier research concepts into practical implementations, building and optimising state-of-the-art AI models such as Transformers, GNNs and diffusion models, plus the codebases, data pipelines and infrastructure for training and evaluation. The role sits in an interdisciplinary team of drug discovery experts and ML specialists, with a strong emphasis on experimentation, benchmarking and taking models from conception to production.

JAX · PyTorch · XLA +6

• London
• Hybrid · 3 days in office
• Senior · manages people

You will design and develop LLM applications for drug discovery, working with research scientists and engineers on model architectures, post-training, reasoning, agents and reinforcement learning. The role spans core ML research, scaling training and inference frameworks, and potentially leading standalone projects with technical mentorship.

JAX · PyTorch · TensorFlow +3

• London
• Hybrid
• Entry level
• Permanent

Early-career scientist role in a Life Sciences team, generating therapeutic hypotheses by mining in-house genomic data with statistical methods to identify and triage drug targets. Also develops and optimises polygenic risk score tools for patient stratification, working with omic data using statistical and AI/ML approaches and communicating findings to internal and external stakeholders.

Git · GitHub · WDL +4

• London
• Hybrid
• £67,900 – £126,100 pa
• Lead · manages people

Lead and develop a global regulatory team delivering clinical trial submissions and approvals, combining people leadership with regulatory expertise. Drive process improvement, simplification and automation while building stakeholder partnerships across Regulatory Affairs. Hybrid role with remote option for UK candidates over 50 miles from the London office.

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.

• London
• £39,560 – £45,641 pa
• Permanent

Deliver theoretical and laboratory-based teaching in clinical biochemistry, haematology and/or blood transfusion across a range of academic levels, while contributing to the School of Science's research profile and student experience. The post sits within the University of Greenwich academic division under the newly formed LASE University Group, based at the historic Medway campus in Chatham.

HCPC

• London
• Hybrid
• Entry level
• Temporary

A one-year PhD fellowship within an International Regulatory Affairs team, supporting development programs and marketed products. The fellow helps build and implement regulatory strategy, prepares and submits applications to local health authorities under supervision, and reviews regulatory intelligence to keep submissions compliant. Based at the London headquarters with hybrid or on-site working options.

• London
• On-site
• £33,000 – £38,000 pa
• Mid-level
• Permanent

Onsite role at a Central London hospital, troubleshooting, installing, maintaining, calibrating and repairing medical equipment, plus completing preventative maintenance and upgrades within set timeframes. Supports the site manager and team leader in meeting contractual KPIs, working to manufacturer guidelines on mechanical, electromechanical and electronic devices.

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

Lead CMC regulatory strategy for UK-manufactured and UK-licensed mRNA products across development, registration and post-approval lifecycle. Act as primary point of contact with the MHRA, oversee submissions and manufacturing change assessments, and shape global regulatory approaches across cross-functional matrix teams.

MHRA · Generative AI

• London
• On-site
• Director

Shape global CMC regulatory strategy for an innovative mRNA medicines portfolio, driving international submissions and health authority interactions. Prepare and review CMC sections of regulatory filings, advise Manufacturing and Quality teams, and oversee multiple development programs. An individual contributor role with global reach, working alongside teams using digital and Generative AI tools.

Generative AI

• Stevenage
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular and vascular programs across early and later phase studies, shaping clinical development plans, study designs and translational strategies. Provides medical monitoring and safety oversight, leads the clinical matrix team, and engages with regulators, KOLs and cross-functional partners in a hybrid working model.

• Waltham, United States
• Hybrid · 2 days in office
• US$284,625 – US$474,375 pa
• Director · manages people

Leads clinical development medical activities for cardiovascular and vascular programs across early and later phase studies, shaping clinical development plans, study designs and translational strategies. Serves as clinical lead for a matrix team, providing medical monitoring, regulatory input and safety oversight while working with biology, regulatory, commercial and operations colleagues.

• London
• On-site
• Director
• Permanent

Senior project manager role coordinating a multi-year osteoporosis drug discovery programme across target ID, hit-to-lead, lead optimisation and candidate selection. Involves orchestrating matrixed wet lab, ML, data science and engineering teams plus CROs, managing plans, budgets, risks and governance, and translating scientific objectives into integrated timelines and milestones.

MS Project · Smartsheet · Asana +1

• London
• Permanent

Builds and scales generative and predictive models of cellular behaviour, acting as the bridge between ML theory and implementation. Day to day involves optimising large neural networks, distributed multi-GPU training, profiling GPU workloads, and productionising research code for multi-modal biological data.

PyTorch · CUDA · Triton +3

• 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