Biotechnology Jobs

• London
• Hybrid
• Director · manages people

Leads GSK's Forward Deployed Engineering function for CMC R&D, setting strategy, hiring and mentoring engineers, and owning senior BU sponsor relationships. Personally contributes to strategic engagements building digital twins, physical AI and self-driving lab capability, using AI coding agents as the primary development mode.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• USA - Pennsylvania - Upper Providence
• Hybrid
• Director

Senior individual-contributor role building a cardiovascular and cardiometabolic translational biology strategy within a respiratory and immunology research unit. Involves defining human-relevant mechanistic hypotheses, biomarker strategies, target evaluation, and business development diligence, with matrix influence across clinical, genetics, and portfolio teams.

• London
• Remote
• Mid-level
• Permanent

Field-based medical affairs role acting as a scientific partner to healthcare professionals and thought leaders across the East Midlands, Yorkshire and East of England. Involves non-promotional scientific exchange, medical education, advisory boards, and supporting investigator-sponsored and real-world evidence studies within a neuroscience portfolio, working closely with UK, Ireland and global teams.

ABPI Code

• Oxford
• On-site
• Temporary

Serve as engineering owner for GMP manufacturing equipment at Moderna's Harwell facility, supporting the Norwood (MA) network. Provide hands-on floor support, troubleshoot complex mechanical and process issues, lead CAPAs and change controls, and drive continuous improvement and tech transfer for mRNA production. Requires close cross-functional work with equipment SMEs and end users.

TMIX · Single Use Mixers · Buffer Prep Vessels +4

• Oxford
• On-site
• Senior

Sole-contributor scientist role developing and executing biochemical and molecular biology assays for PK/PD analysis, spanning genomic DNA/RNA isolation, qPCR, ddPCR, RNA sequencing, MSD, ELISA and immunoblotting. Works within Moderna's Clinical Bioanalytical team at Harwell, Oxfordshire, ensuring GcLP-compliant assay qualification and validation, troubleshooting with external CRO partners, and building internal and external mRNA-based bioanalytical capability.

MSD · LIMS · eLNB +1

• London
• Hybrid
• Lead
• Permanent

Provide scientific leadership across model evaluation and applied use cases, ensuring foundation models stay grounded in drug development and translational research challenges. Act as a senior individual contributor and key scientific partner, mentoring junior colleagues and working with Product and Business Development to turn biology and ML into customer-facing deliverables as the team scales.

• United Kingdom
• Remote
• Director · manages people

Senior medical leadership role within a clinical research organisation, acting as a cardiovascular subject matter expert supporting proposals, bid defences and client engagement. Responsibilities span RFP input, protocol and regulatory strategy, internal therapeutic training, and mentoring clinical scientists, with peer-level interaction with pharma medical leadership.

PPD

• Glasgow
• £39,906 – £46,049 pa
• Entry level
• Contract

Develops high-throughput Python workflows to analyse coarse-grained molecular-dynamics simulations of engineered protein assemblies, extracting geometric, topological and structural descriptors such as curvature, lumen dimensions and packing order. Builds structure-property relationships and reusable, version-controlled pipelines feeding predictive and active-learning models, within an interdisciplinary team spanning computational chemistry, machine learning, protein science and engineering.

Martini · GROMACS · VMD +2

• Harrow
• Hybrid
• Mid-level

Drives strategic impact by developing operational and technical solutions for Early Phase clinical trials, collaborating with Enterprise Accounts, Growth Accounts, Commercial Operations and Strategic Business Units. Contributes to business development from opportunity identification through solution design, bid strategy and client engagement, crafting differentiated value propositions and proposal content. Requires 3-5 years of Early Phase Clinical Trials experience and up to 30% travel.

Clinical Trial Management Systems · Proposal Development Platforms · Enterprise Software Solutions

• Exeter
• Entry level
• Contract

Computational PhD project using cell-free DNA sequencing to infer placental gene activity and dissect how genetic variants linked to adverse pregnancy outcomes affect placental function. The student develops tools to map nucleosomal footprints, integrates them with single-cell RNA-seq markers and GWAS summary statistics, and may generate new plasma data.

scRNA-seq · cfDNA Sequencing · GWAS

• London
• On-site
• £47,500 pa
• Entry level
• Contract

Investigates how protein machines remodel microtubules using cryo-electron microscopy, protein reconstitution and fluorescence microscopy. As an early member of a new lab, you will shape the research programme, establish experimental approaches and develop scientific independence while working closely with the group leader.

Cryo-EM

• London
• Hybrid
• £68,284 – £76,244 pa
• Senior
• Permanent

Develops and leads an AI-driven research programme in biomolecular design and molecular interactions, spanning protein-ligand, protein-protein and protein-nucleic acid systems. Combines structural biology, biophysics, quantitative biology and machine learning, while teaching computational biology and biomolecular design at undergraduate and postgraduate level, including a new MRes in AI for Bioscience.

• London
• Hybrid
• Senior

Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.

CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3

• United Kingdom
• Remote
• Lead · manages people

Leads global regulatory strategy for Phase 1-4 clinical trials, preparing and assembling CTA submissions and acting as the client-facing liaison with sponsors and regulatory agencies. Represents the regulatory department in bid defense and launch meetings, managing project teams and reviewing clinical and scientific documentation.

Microsoft Word · Microsoft Excel · PowerPoint

• London
• Lead

Serves as subject matter expert in COA endpoint strategy, instrument development and regulatory strategy, advising pharma and biotech sponsors and representing the company as an external scientific thought leader. Leads qualitative research supporting content validity, oversees internal project teams, mentors consultants and supports business development through proposals and client presentations.