Biotechnology Jobs

• Oxford
• On-site
• Senior · manages people
• Permanent

Lead a flagship research programme in advanced genome technologies, focusing on novel plant transformation, regeneration and DNA/RNA delivery systems. Build and manage an interdisciplinary team of group leaders, postdocs and PhD students, driving stage-gated projects and translating findings into commercial and IP opportunities.

• Oxford
• On-site
• Lead
• Permanent

Lead the design and deployment of AI, robotics and computer vision systems to accelerate plant transformation and tissue culture workflows. Provide plant science subject matter expertise within a matrixed team, build data pipelines for predictive ML models, and manage project plans while mentoring researchers and driving commercial translation.

• London
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation across Phase I–III studies. Partners with Senior Scientists and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

AI

• Mississauga, Canada
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams, leading medical monitoring and safety oversight for lung and head/neck cancer studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, regulators and cross-functional matrix teams across Phase I–III development.

• United Kingdom
• Remote
• Senior

Accountable for delivering clean clinical data on complex internal medicine trials within contract timelines, managing operational and quality aspects in compliance with ICH GCP. Leads clinical teams, develops monitoring tools and Trial Master File documentation, and may take on Lead CTM or Clinical Study Manager duties across therapeutic areas.

Outlook · Excel · Word

• Swindon
• On-site
• Entry level
• Permanent

Supports the routine running of a QC Microbiology laboratory: booking in samples, maintaining reagent, media and consumable stock, ordering supplies, performing equipment checks and second-analyst checks, and helping clean classified cleanrooms. Also writes and updates SOPs, specifications and scientific reports while working to GMP standards. No previous laboratory experience is required.

Microsoft Word · Microsoft Excel

• London
• Hybrid · 3 days in office
• Senior

Lead translational pharmacology for an AI-first drug discovery team, shaping neurodegeneration strategy and target validation. Bridge dry-lab predictive models with experimental biology, designing screening cascades and profiling AI-designed molecules. Manage CRO partnerships and serve as scientific lead for portfolio programs.

SPR · TR-FRET · Mass Spectrometry

• London
• Hybrid · 3 days in office
• Senior

Operating Partner supporting VPs of AI on high-priority strategic initiatives, acting as a trusted advisor and operational force-multiplier. The role involves translating complex machine learning concepts into executive communications, driving cross-functional alignment without line authority, and unblocking inefficiencies across research, engineering, product and operations in a fast-scaling environment.

AlphaFold

• Manchester
• On-site
• Entry level

Perform complex clinical procedures such as ECG, phlebotomy, spirometry, cannulation and cardiac telemetry on trial volunteers, and collect and report data per protocol. Support Phase I-IV studies at a hospital-based research facility, ensuring compliance with GCP and SOPs while orienting volunteers and assisting nursing colleagues.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• 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

Perform routine cGMP Quality Control testing using HPLC, UPLC, GC, UV spectroscopy, DLS and Karl Fischer analysis, supporting raw materials, in-process materials, drug substance, product release and stability programs. Coordinate and execute global GMP stability studies, manage sample lifecycles in LabVantage LIMS, trend data statistically, and author protocols and regulatory documentation. The role is 100% onsite at the Harwell facility and involves collaboration with manufacturing, QA, regulatory and external testing partners.

LabVantage · LIMS · Generative AI

• Oxford
• On-site
• Senior

Provides hands-on MS&T engineering expertise across drug substance manufacturing and label, packaging and final-storage operations at the Harwell site. Leads technology transfer, process start-up, validation, continued process verification and troubleshooting, authoring protocols and reports as an individual contributor. Works cross-functionally with Manufacturing, Quality and Supply Chain, with on-call or shift coverage as required.

SAP · VEEVA · DeltaV +4

• Leeds
• Director · manages people

Owns product strategy, roadmap and innovation for clinical pharmacology clinics and bioanalytical labs, spanning early-phase platforms like ClinSpark, LIMS/LIS, ELN, instrument connectivity and lab automation. Builds business cases and secures funding, governs a regulated portfolio, and leads multidisciplinary product teams and vendors across distributed sites.

ClinSpark · LIMS · LIS +7

• 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.

• Cambridge
• Director · manages people

Leads end-to-end Clinical Systems migration initiatives such as CTMS, eTMF and study startup, from strategy and due diligence through implementation, cutover and legacy decommissioning. Oversees data migration programs, CRO integrations and GxP validation, managing vendors, stakeholders and a team of professionals while shaping the Clinical Systems roadmap.

CTMS · eTMF