Biotechnology Jobs

• Stevenage
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds external expert relationships and represents the company at advisory boards and medical meetings.

• Zug, Switzerland
• On-site
• US$284,250 – US$473,750 pa
• Director

Leads clinical development for GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds external expert relationships and represents the company at advisory boards and medical meetings.

• Opfikon, Switzerland
• Hybrid · 3 days in office
• US$317,000 – US$409,000 pa
• Director · manages people

Leads the cross-functional Clinical Development Team as lead scientific expert, owning the Clinical Development Plan and integrating internal and external contributions into program strategy. Serves as medical monitor, authors key regulatory and study documents, and presents to safety and review committees.

• Harrow
• Remote
• Senior

Acts as principal labelling strategist within Global Regulatory Affairs, driving development and maintenance of dCCDS, CCDS, USPI and EU SmPC documents across an assigned product portfolio. Leads Global Labeling Committee reviews of proposed label exceptions and represents labelling on regulatory strategy teams, working with safety, clinical and commercial stakeholders. Home or office based across European locations.

Company Core Data Sheet (CCDS) · Development Company Core Data Sheet (dCCDS) · US Prescribing Information (USPI) +3

• Newcastle upon Tyne
• On-site
• Senior

Provides advanced third-level technical support for Digital Pathology products including the Aperio GT Platform, CytoVision and CytoInsight, resolving complex escalations and communicating guidance to field teams. Owns service readiness for change requests and new product development, partnering with R&D, Quality and Product Management to turn findings into documented defects and service improvements.

Aperio GT Platform · Aperio FL · CytoVision +7

• Hemel Hempstead
• Senior

Provides technical support and training to customers using mass spectrometry, LCMS and metabolomics platforms across EMEA. Delivers application optimisation, troubleshooting, presentations and product feedback to R&D, combining scientific expertise with customer engagement and up to 50-75% travel.

• Newcastle upon Tyne
• Hybrid
• Director

Provides medical and clinical leadership for the development of novel diagnostic and companion diagnostic assays and platforms supporting precision medicine. Acts as subject matter expert for R&D projects, clinical studies and regulatory submissions, and supports pharma partnerships and pathology education. Hybrid role based in Newcastle Upon Tyne with 30-40% international travel.

IVD · CDx · Digital Pathology

• US - East Coast
• Director · manages people

Leads identification, evaluation and execution of strategic partnerships, licensing, M&A and co-development deals, from sourcing through due diligence, structuring and closing. Represents the company to biotech, pharma and academic partners, monitors competitive and market dynamics, and advises executive leadership on external innovation strategy post-launch.

• London
• On-site
• Senior

Owns all aspects of hardware design for automated cell-production machines, from concept through to manufacture, improving robustness and reliability. Leads development of systems interfacing with optics and fluidics, refines test rigs and quality processes, and helps shape engineering culture. Based on-site in the lab at Imperial College's White City innovation hub.

Arduino · Raspberry Pi · Adafruit +1

• London
• Hybrid
• Director · manages people

Leads the global and US Medical Affairs Neuro-Oncology team, owning medical strategy, evidence generation and launch planning for pipeline and marketed assets. Serves as a key interface between Medical Affairs and R&D, clinical development and commercial functions, representing regional insights in governance forums. Combines people management with hands-on execution across a complex matrix.

• 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.

• Sheffield
• Remote
• Senior

Leads research design and analytical strategies for clinical trials, developing and reviewing statistical analysis plans and authoring reports, abstracts and manuscripts. Acts as functional lead on study teams, directing biostatistical activities, performing complex analyses in SAS or R, and quality-controlling deliverables while mentoring junior staff and liaising with clients on scope and budget.

SAS · R

• 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
• Senior

Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.

CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3

• London
• On-site
• Mid-level

Owns end-to-end purchasing, invoicing and inventory for both electromechanical automation systems and GMP-grade sterile fluidic consumables, spanning supplier qualification, cost-down programmes and demand planning. Reports to the Hardware Lead and works across manufacturing, biology, engineering, quality and finance, building ERP/MRP-based planning in a hands-on, on-site role.

ERP · MRP