Biotechnology Jobs

• Slough
• On-site
• Mid-level
• Permanent

Performs routine, non-routine and stability testing of biologic drug substances in a client's Analytical Service Department, running ELISA, cell-based and Biacore assays and capturing data in laboratory software and electronic notebooks. Generates and reviews GMP-compliant documentation, SOPs and protocols, supports method development and validation, and handles out-of-specification investigations while liaising with internal and external clients.

Biacore · Vi-Cell · Microsoft Office

• Slough
• On-site
• Senior
• Permanent

Performs routine, non-routine and stability testing of biologic drug substances using ELISA, cell-based potency assays and Biacore (SPR), while coordinating assay activities and managing project priorities and timelines. Acts as a technical subject matter expert, mentoring colleagues and supporting method development, validation, troubleshooting and GMP-compliant documentation within a client-facing analytical service department.

ELISA · Biacore · Vi-CELL +2

• Hemel Hempstead
• Senior

Provides technical support and training to customers using mass spectrometry, LCMS and metabolomics platforms across EMEA. Delivers application optimisation, troubleshooting, presentations and product feedback to R&D, combining scientific expertise with customer engagement and up to 50-75% travel.

• Oxford
• On-site
• Permanent

Builds computational tools and data analysis pipelines for plant biology, working at the intersection of multi-omic analysis and software development. Integrates transcriptomics, metabolomics, proteomics and imaging data, developing pipelines for image segmentation, feature extraction and phenotyping, and preparing datasets for agentic workflows. Collaborates closely with bioinformaticians, research scientists and AI engineers in the Bioinformatics platform team.

• Oxford
• On-site
• Junior
• Permanent

Hands-on bench role executing microbial culture, identification, biobanking and broth microdilution antimicrobial susceptibility testing under BSL-2 conditions, compliant with EUCAST/CLSI guidelines. Works within a highly automated reference laboratory integrating robotics and data systems, with scope to help design and optimise high-throughput workflows alongside microbiologists, genomics scientists and automation engineers.

MALDI-TOF · Oracle · Long-Read Sequencing +1

• 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

• 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
• Hybrid · 2–3 days in office
• Senior

Embedded with Chemical Manufacturing & Control teams, you take high-priority use cases from problem framing to working prototypes at days-to-weeks cadence, then hand proven solutions to a Solutions Engineer for scale-up. Work is AI-augmented: agent frameworks, multi-agent orchestration, MCP, and AI coding assistants are the default mode of building, turning manual lab and process workflows into agentic automation.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• London
• Senior
• Permanent

Builds generative and predictive models of cellular behaviour from high-content imaging, curating cell painting and brightfield datasets and designing evaluation that separates biological signal from technical artefact. Partners closely with ML scientists and wet lab assay teams, linking imaging readouts to single-cell and perturbation data in a matrixed TechBio environment.

NumPy · pandas · Polars +6

• London
• On-site
• Senior
• Permanent

Processes and quality-controls paired single-cell RNA-seq and scATAC-seq data at scale, building Nextflow pipelines for custom combinatorial indexing chemistries and integrating multimodal datasets for GPU-accelerated model training. Partners with wet lab scientists and ML modellers to design evaluation frameworks and biological benchmarks, bridging experimental and computational teams in a matrixed TechBio environment.

STARsolo · Alevin-fry · Chromap +5

• London
• Remote
• Director

Provides statistical consulting and strategic advice on optimal study designs and analyses across drug, device, and diagnostic clinical development, including preparation for regulatory authority interactions. Serves as a leader in innovative study designs for client accounts and supports new business through proposals, bids, and client presentations, representing clients at key regulatory meetings.

FDA · EMEA · MHRA +2

• Cambridge
• On-site
• £42,254 – £56,535 pa
• Mid-level · manages people
• Contract

Manage a small sub-team fulfilling genomic data requests, defining cohorts from genomic profiles and delivering datasets to researchers. Work spans LINUX/UNIX, HPC, scripting in Python, R and Bash, Git, and database management, with datasets moving from CSD3 to AWS and a commercial bioinformatics platform. Also contributes to wider Bioinformatics team activities.

AWS · CSD3 · Git

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

Lead end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory and global distribution for an AI-first drug discovery company. Act as the clinical supply authority within a lean Pharmaceutical Sciences & CMC team, building scalable systems and vendor networks while partnering closely with Clinical Operations and CROs.

IRT · RTSM

• Seqirus USA - NC - Holly Springs
• Lead

Owns quality oversight of external CROs, laboratories and test facilities supporting nonclinical and GLP activities, running the full vendor lifecycle from due diligence and quality agreements to risk-based monitoring, CAPAs and governance forums. Coordinates inspection readiness and audit support, ensures compliance with GLP/GCP/GMP, OECD GLP, 21 CFR Part 58 and ALCOA+ data integrity, and leads vendor risk assessments such as FMEA and risk registers.

OECD GLP · 21 CFR Part 58 · Annex 11 +3

• Maidenhead
• Lead

Owns quality oversight of external CROs, laboratories and test facilities supporting nonclinical and GLP activities, running the vendor lifecycle from due diligence and quality agreements to risk-based monitoring, CAPAs and inspection readiness. Ensures adherence to GLP/GCP/GMP, OECD GLP, 21 CFR Part 58 and data integrity (ALCOA+), partnering with Nonclinical Development, Procurement, Legal and IT.

OECD GLP · 21 CFR Part 58 · Annex 11 +3