Biotechnology Jobs

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

Lead a flagship plant biotechnology research programme focused on photosynthesis, carbon assimilation and nitrogen fixation to boost crop yields and cut inputs. You will coach and oversee Group Leaders, run your own independent research, recruit scientists and postdocs, and drive stage-gated projects toward commercial and IP impact within a rapidly scaling institute.

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

Design, roll out and maintain an ISO 9001-aligned Quality Management System across a research institute, covering document control, audit programmes and management reviews. The role also involves delivering QMS training and acting as a trusted advisor to programme leaders, on a 12-month fixed term contract.

• Zug, Switzerland
• On-site
• US$242,550 – US$404,250 pa
• Director · manages people

Senior physician leader providing medical oversight, safety evaluation and clinical data interpretation across lung cancer studies within a clinical programme team. Partners with the Senior Scientist and cross-functional groups on protocol design, regulatory interactions and external scientific engagement, while mentoring Medical Directors. Requires an on-site presence of at least two days a week at a GSK site.

• Waltham, United States
• Hybrid · 2–3 days in office
• US$222,750 – US$371,250 pa
• Director

Serves as the physician on 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 a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

AI

• United Kingdom
• Hybrid
• Mid-level

Manages end-to-end clinical trial supply chains, developing study-specific plans, coordinating cross-functional teams, and ensuring GxP-compliant distribution and inventory levels. Represents the department externally, mentors junior staff, and drives process improvements within a global clinical supplies team.

Microsoft Office

• United Kingdom
• Remote
• Lead

Supports central comparator sourcing for clinical trials on a client-dedicated FSP team, covering market intelligence, sourcing recommendations, and purchase order execution across EMEA. Acts as an SME on the external comparator landscape, advising on regional and central/local sourcing strategy while escalating quality or temperature issues to the client.

• London
• Hybrid · 3 days in office
• Mid-level

Join the Compute Infrastructure team to keep a planet-scale GPU accelerator fleet healthy and efficient. You'll build observability and telemetry pipelines, automate recovery, hunt compute waste, and optimise accelerator utilisation for large-scale training and inference, working closely with ML infrastructure and research teams.

GCP · Kubernetes · Nvidia GPU +1

• London
• Hybrid · 3 days in office
• Lead

Lead medicinal chemistry strategy across drug discovery programmes, from hit identification through lead optimisation to candidate nomination, while working hands-on as an individual contributor. Partner closely with AI/ML platform teams to shape predictive models, manage CRO resources and KPIs, and represent the company externally with collaborators.

AlphaFold

• Haywards Heath
• Hybrid · 3 days in office
• Director · manages people

Leads a global team of development and regulatory project managers overseeing complex R&D programs across a therapeutic area, including new product development and life cycle management. Drives portfolio planning, risk assessment, and cross-functional alignment as part of the Portfolio & Operations Excellence leadership team, with hands-on coaching and process improvement.

Microsoft Project · Planview · Smartsheet +1

• York
• Hybrid
• £38,448 – £46,970 pa
• Entry level
• Contract

Lead an ARIA-funded project characterising engineered lipid nanoparticles that target lung-mediated immune regulation, with a focus on macrophage-driven innate immune mechanisms. Work spans mouse models, flow cytometry and fluorescence microscopy within a multi-university consortium, based at York with some remote working.

Flow Cytometry · Fluorescence Microscopy

• London
• Remote
• Senior · manages people

Leads cross-functional clinical trial teams for biotech clients, owning project plans, budgets, P&L, risk management and client relationships from Phase I to III. Requires strong CRO experience and therapeutic expertise in oncology plus areas such as dermatology, women's health, neurology, rare disease or radiopharmaceuticals, working fully remotely within a select EMEA country.

Microsoft Excel · PowerPoint · Microsoft Word +1

• 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

• Livingston
• Mid-level

Leads strategic sourcing of animal models, especially rodents and genetically engineered strains, for an early-phase discovery business. Manages supplier relationships, RFIs/RFPs, contract negotiations and performance reviews, while partnering with scientific, veterinary and quality teams on capacity planning, welfare and regulatory compliance.

• Abingdon
• On-site
• Entry level
• Permanent · Shift work

Operate pilot plant reactors and ancillary equipment in a GMP-regulated large-scale chemical production environment, running multiple syntheses, some never previously scaled. Duties include routine maintenance and reconfiguration of reaction vessels, environmental monitoring, accurate batch documentation, and shift handovers. The role follows a rotating 12-hour day and night shift pattern averaging 42 hours per week.

Microsoft Office

• Reading
• Mid-level

Conducts site monitoring visits including selection, initiation, monitoring and close-out, ensuring compliance with GCP and ICH guidelines. Manages site recruitment plans, protocol training, regulatory submissions and data query resolution, maintaining Trial Master File documentation. Focused on oncology studies within a biotech-focused clinical research team.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint