Biotechnology Jobs

• Stevenage
• 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 ship first production versions. Work is AI-augmented: agent frameworks, multi-agent orchestration, MCP and AI coding assistants handle routine coding while you supply judgement and validation, coaching BU engineers along the way.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

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

Embedded with chemical manufacturing and control teams, you take high-priority AI use cases from problem framing to working prototype at days-to-weeks cadence, then hand proven solutions to a solutions engineer for scale-up. The work centres on Physical AI: self-driving labs, lab automation and robotics, digital-to-physical orchestration, and simulating manufacturing lines and tech transfers in NVIDIA Omniverse and Isaac Sim. AI coding agents handle much of the routine coding, leaving you to frame problems, apply judgement and validate results.

NVIDIA Omniverse · Isaac Sim · Nemotron +7

• Cambridge
• Mid-level · manages people

Lead client-facing formulation development programmes for biologic drug products, combining hands-on lab science with project ownership and people management. Design and oversee complex experimental studies, manage client interactions and technical reports, and mentor scientists within a growing team while driving innovation and technical excellence.

• Larbert
• Lead · manages people

Lead the development of next-generation electrochemical biosensors and diagnostic assays while remaining hands-on in experimental design, data interpretation and sensor development. The role spans electrochemistry, sensor engineering, biofunctionalisation, assay development and manufacturability, working with scientists, engineers and commercial teams to turn concepts into viable diagnostic products. It combines scientific leadership and mentoring with deep technical involvement rather than pure management.

• Cambridge
• Lead

Lead complex formulation development programmes for biologics, acting as subject matter expert and providing technical oversight across multiple client projects. Design experimental strategies, present findings to clients and external stakeholders, and mentor junior scientists within a multidisciplinary team.

• London
• Hybrid
• £49,140 – £91,260 pa
• Lead · manages people

Leads statistical programming strategy across multiple trials or a full program, acting as Trial, Lead or Program Programmer and coordinating internal and external programmers. Develops and validates CDISC-compliant datasets and outputs for CSRs, regulatory submissions and safety reports, using R, SAS or Python, Git-based version control and reproducible workflows. Also shapes standards, templates and governance, with hybrid working from London.

R · SAS · Python +4

• Home Worker
• Remote
• £49,140 – £91,260 pa
• Lead · manages people

Leads statistical programming strategy for clinical trials and programs, acting as Trial, Lead or Program Programmer and coordinating internal and external teams. Develops and validates CDISC-compliant datasets and outputs for regulatory submissions, using R, SAS or Python, Git-based version control and reproducible workflows. Also shapes standards, templates and governance across studies.

R Shiny · Tidyverse · Git +2

• Aylesbury
• £23 ph

Job summaryWe have an exciting opportunity for a Biomedical Scientist Microbiology at Buckinghamshire Healthcare NHS Trust to join the Microbiology Department at Stoke Mandeville Hospital. You will be responsible for performing specialist microbiology and serology investigations in accordance with departmental…

• London
• Hybrid
• Senior
• Permanent

Enterprise sales role focused on landing new logos across pharmaceutical and biotech companies, owning the full cycle from prospecting to close. Involves navigating complex multi-stakeholder deals with scientific, technical, procurement and executive buyers, and translating an AI-native biology platform into customer value. Partners closely with founders, product and science teams to refine go-to-market playbooks.

• Oxford
• On-site
• Mid-level
• Temporary

Hands-on individual contributor role operating production equipment for mRNA vaccine manufacturing at the Harwell site, following cGMP, SOPs and safety requirements. Involves troubleshooting equipment and digital issues, basic maintenance, documentation with Quality Assurance, and RCA/CAPA investigations, with exposure to continuous improvement and Generative AI tools.

Generative AI

• Sheffield
• Remote
• Lead

Configures, tests and maintains electronic Clinical Outcome Assessment studies in platforms such as Medidata Designer eCOA, translating protocols and licensed instrument requirements into questionnaires, schedules and branching logic. Acts as technical contact for sponsors and vendors, coordinates eCOA-to-EDC integration and deployment, and mentors less-experienced study designers across multiple global trials.

Medidata Designer eCOA · Medidata Rave

• London
• Hybrid
• Senior
• Permanent

Leads global pharmacovigilance operations, overseeing case intake, ICSR processing and regulatory reporting across clinical and post-marketing portfolios. Acts as business administrator for the Veeva Safety database and primary interface with PV vendors, while driving SOPs, inspection readiness and safety data exchange agreements.

Veeva Safety

• London
• Hybrid
• Mid-level

Drives clinical supply forecasting and IMP budgeting for global trials, translating study protocols and recruitment projections into forecasting tools and monitoring deviations over 3-12 month horizons. Coordinates cross-functional IMP estimation and risk assessment meetings, aligning manufacturing, packaging and distribution to prevent stock-outs, while leading continuous improvement in a matrixed environment.

RTSM · Excel

• London
• Hybrid
• Senior

Leads regional or global regulatory strategy for development programs and marketed products, serving as a regulatory lead and primary contact with health authorities. Manages preparation, submission and approval of regulatory applications, advises teams on approval pathways and expedited routes, and monitors regulatory intelligence to inform strategy.

• United Kingdom
• Remote
• Mid-level

Coordinates and oversees clinical trial activities for assigned studies, including regulatory document review, (e)TMF management, and site file compilation. Provides finance support such as raising POs, vendor creation, budget tracking and invoicing using CERPS, Ariba, Fiori and Veeva Payments. Trains new staff and works within a matrixed FSP team.

Veeva Payments · CERPS · Ariba +5