Biotechnology Jobs

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

Designs and implements translational strategies for small molecule oncology and immunology programs, from early discovery through candidate selection and clinical phase. Oversees CRO activities, PK/PD and safety assessments, and biomarker strategies, bridging computational predictions with laboratory validation. Some roles include managing 2-3 in vivo pharmacologists.

Machine Learning · AlphaFold

• London
• Hybrid · 3 days in office
• Senior

Contribute to the design of novel large-molecule therapeutics by applying computational and machine learning methods to predict biologics properties such as affinity, developability and immunogenicity from sequence. Work within an interdisciplinary computational sciences team alongside ML and biologics discovery experts, benchmarking models, analysing lab data and shaping data-generation strategies for active learning.

AlphaFold

• Stevenage
• Director

Accountable for GSK R&D's enterprise portfolio of external scientific content and data licenses, managing budget, forecasting, cost controls and vendor commercial terms. Acts as senior interface to information providers and connector across scientific, procurement, legal, copyright and technology teams, ensuring copyright-compliant use and positioning content for AI and text-mining exploitation.

Excel · PowerPoint · Word +2

• USA - Pennsylvania - Upper Providence
• Director

Accountable for GSK R&D's enterprise portfolio of external scientific content and data licenses, including budget, forecasting, cost controls and retiring under-used sources. Manages vendor relationships and commercial terms, maintains copyright-compliant governance and user guidance, and works across scientific, procurement, legal, digital and technology teams to make licensed content AI- and text-mining-ready.

Excel · PowerPoint · Word +2

• Reading
• Mid-level

Monitors clinical trial sites across the UK, performing selection, initiation, monitoring and close-out visits in line with GCP and sponsor requirements. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains TMF/ISF documentation. Dedicated to a single sponsor within IQVIA's cFSP model.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Manchester
• Mid-level

Monitors clinical trial sites through selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines, while driving subject recruitment and tracking regulatory submissions, CRF completion and data queries. Works within a full-service, multi-sponsor site management team, training site staff and maintaining Trial Master File documentation.

• Leeds
• On-site
• Entry level
• Permanent

Prepare and handle investigational medicinal products in a cGMP clean room, applying sterile technique and GMP during live first-in-human studies. Work in pairs with Technical Officers on study set-up, dose calculations, batch records and equipment checks, with the clinic and pharmacy under one roof at an MHRA-accredited Phase I unit.

Outlook · Word · Excel +1

• Maidenhead
• Lead · manages people

Client-facing biostatistics role leading design and analysis of non-interventional and low-interventional studies using real-world data such as claims, EHR and registries. Applies causal inference methods, target trial emulation and synthetic control arms, authors SAPs and manages SAS programming teams, while supporting proposals, budgeting and bid defences.

SAS · CDISC

• Oxford
• On-site
• Mid-level
• Contract

Designs and delivers immunogenicity and bioanalytical strategies for regulated clinical programmes, developing ADA, nAb, PK and PD assays using ELISA, MSD and cell culture. Works with multidisciplinary teams to validate assays, manage reagents and SOPs, and integrate digital and AI-enabled tools. Site-based at Harwell within a growing mRNA-focused team.

ELISA · MSD · LIMS +2

• Cambridge
• Hybrid · 3 days in office
• Director

Leads an integrated Business Continuity and Crisis Management capability across Oncology R&D, owning the framework, risk registers and BIAs while designing executive-level crisis exercises. Drives emerging-risk assessment, supply-chain nth-tier visibility and the practical use of AI in resilience practice, acting as the audit and regulatory interface for standards such as NIS2.

NIS2 · Business Continuity Software

• Cambridge
• Hybrid
• £35,000 – £45,000 pa
• Mid-level

Develops FPGA and embedded firmware for high-performance data acquisition and signal processing systems used in biomedical research products. Writes VHDL for FPGA design and C for low-level hardware control, integrating with interfaces such as SPI, I2C, UART, USB and Ethernet. Works alongside hardware and software engineers across the full product lifecycle, with real project ownership and a progression route to senior roles.

AMD/Xilinx Vivado · Intel Quartus · USB +1

• Oxford
• On-site
• Mid-level

Hands-on automation engineering role supporting drug product packaging and drug substance manufacturing at a new mRNA facility. Involves commissioning and optimising Emerson DeltaV and Allen-Bradley/Rockwell PLC systems, automated labelling and secondary packaging equipment, plus GxP validation, root cause analysis and lifecycle documentation. Works independently as a technical specialist across manufacturing, engineering, quality and digital teams.

Emerson DeltaV · Allen-Bradley · Rockwell Automation +7

• Cambridge
• Hybrid · 3 days in office
• Lead

Designs and builds end-to-end AI and optimisation solutions, including mathematical optimisation, modelling and simulation, for complex pharmaceutical business problems. Works in a global team of AI engineers, data scientists and software developers, visualising model outputs and championing software engineering best practices such as Python, CI/CD and testing.

CPLEX · Gurobi · SCIP +1

• United Kingdom
• £55,000 – £70,000 pa

This role involves leading in-vitro toxicology studies within a regulated preclinical environment, focusing on assay development and execution for product safety assessment. The scientist will apply advanced cell-based methods including Neutral Red, Ames, and micronucleus assays, interpret complex biological data, and support regulatory submissions. Collaboration with internal teams and external partners is key, alongside method validation and scientific reporting in a quality-assured laboratory setting.

• London
• Hybrid · 2–3 days in office
• Junior

Contribute across a full-stack cloud product and IoT devices that interface with hardware automating human cell production. Work spans TypeScript, React, GraphQL frontends and Node.js/PostgreSQL backends, with cross-disciplinary collaboration alongside hardware engineers and biologists, including testing on prototype machines in the lab.

React · TypeScript · GraphQL +7