Biotechnology Jobs

• Oxford
• On-site
• Entry level
• Permanent

Postdoctoral role in the Zuercher Lab at the Generative Biology Institute, working on genome synthesis and genetic isolation. Involves designing and troubleshooting experiments, analysing complex datasets with computational and statistical tools, publishing papers, and mentoring junior researchers. Based at Oxford Science Park in a new bespoke facility.

E. coli

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

Lead a flagship research programme in biological nitrogen fixation, engineering novel nitrogen-fixing systems into plants through metabolic and protein engineering. Recruit and manage a team of postdocs and PhD students, drive stage-gated translational research from lab to field, and build collaborations across EIT Oxford and commercial partners.

• Stevenage
• 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. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, regulatory interactions and investigator engagement, with on-site presence 2-3 days per week.

AI-enabled insights

• Zug, Switzerland
• 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. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2-3 days per week.

AI-enabled insights

• Swindon
• On-site
• Shift work

Operate aseptic filling lines and manufacture pharmaceuticals to SOPs and Batch Manufacturing Records, performing filling, packaging, in-process checks, line changeovers and cleaning. Work in cleanrooms on Double Days, 24/7 or Night shifts, using HMI-controlled CIP/SIP systems, autoclaves and SAP, and support validation and new product introduction.

SAP · HMI · CIP +2

• United Kingdom
• Remote
• Lead · manages people

Leads global regulatory strategy for Phase 1-4 clinical trials, preparing and assembling CTA submissions and acting as the client-facing liaison with sponsors and regulatory agencies. Represents the regulatory department in bid defense and launch meetings, managing project teams and reviewing clinical and scientific documentation.

Microsoft Word · Microsoft Excel · PowerPoint

• London
• Hybrid · 3 days in office
• Lead

Build and evolve a large-scale ML infrastructure platform that supports training and deploying novel models across vast compute and data pools. Work cross-functionally with research, engineering and product teams, exploring agent deployment and distributed, performance-critical workloads. Hybrid role in London requiring three office days a week.

Kubernetes · Google Cloud Platform · GCP +1

• London
• Hybrid · 3 days in office
• Senior

Join a newly formed LLM Engineering team to architect, build and own scalable, secure infrastructure bringing large language models into scientific and business workflows. Work spans system design, agentic tooling, RAG, evaluation frameworks and fine-tuning, partnering closely with AI researchers and drug discovery experts.

vLLM · MCP · GCP

• Uxbridge
• Hybrid
• Director

Leads EU regulatory strategy for an immunology and cardiovascular portfolio, from early development through registration and lifecycle management. Acts as the regulatory lead for assigned development teams, negotiating with the EMA and other health authorities and building integrated submission plans. Integrates scientific, medical, legal and business perspectives while monitoring European regulatory trends.

EMA

• Livingston
• On-site
• Entry level

Assembles clinical trial test kits with specimen collection materials according to protocol, prepares investigator instruction manuals and flowcharts, and packages completed kits with documentation and ancillary supplies for shipment. Monitors inventory levels and alerts supervisors when supplies run low to prevent study delays. Site-based role requiring strong attention to detail and organizational skills.

• Livingston
• Hybrid
• Mid-level

Coordinates laboratory study setup for a clinical research organisation, covering protocol and budget review, database setup, project plans, timelines and documentation. Presents protocol materials at kick-off and investigator meetings, manages scope changes and budget monitoring, and works with project management to improve processes across global Phase I-IV trials.

• Addlestone
• £47,557 pa
• Permanent

Assesses quality data submitted by companies to support marketing authorisation applications and variations for veterinary medicines, as part of the Quality team within the Pharmaceuticals Section. Also contributes to regulatory science strategy, guideline development, product defect assessment and international training of other regulators.

Microsoft Office 365 · Word · Excel +3

• London
• Mid-level
• Permanent

Deliver and maintain UK competitive licences, lead regulatory strategy for new initiatives, and ensure compliance across defined products and projects. Provide local regulatory expertise for clinical trial approvals, lifecycle submissions and MHRA interactions, contributing to cross-functional teams and study feasibility work.

Veeva · AI

• Oxford
• On-site
• £40,178 – £48,700 pa
• Entry level
• Contract

Conducts research characterising crosslinked proteins and lipids under a Wellcome Trust-funded grant, using proteome and lipidome methods including sample preparation, LCMS and data analysis. Manages project administration, guides junior researchers and students, and contributes to reports, publications and external seminars.

LC-MS · nanoLC-MS

• London
• Hybrid
• Entry level
• Temporary

A one-year PhD fellowship within an International Regulatory Affairs team, supporting development programs and marketed products. The fellow helps build and implement regulatory strategy, prepares and submits applications to local health authorities under supervision, and reviews regulatory intelligence to keep submissions compliant. Based at the London headquarters with hybrid or on-site working options.