Biotechnology Jobs

Isomorphic Labs · Cambridge, United States

Lead the safety assessment strategy for small molecule and biologic drug discovery projects from inception to regulatory submission, designing screening cascades and mechanistic experiments. Partner with machine learning researchers to build predictive toxicology models and manage CRO relationships for outsourced wet-lab data generation, while mentoring junior team members.

Mytos · London

Open general application for a London-based biotech automation company building machines that fully automate human cell production. The team, drawn from ex-Dyson engineers and Nature-published scientists, seeks people with a track record of solving hard technical or non-technical challenges, low ego and high curiosity, including those starting their first job.

EMBL-EBI · Saffron Walden

Lead solution architecture for digital experience initiatives spanning web applications, APIs, content platforms and AI-enabled services, remaining hands-on through discovery, prototyping and architectural development. Bridge UX and engineering, translating user needs into accessible, sustainable architectures while providing technical direction and people management to the development team. Focus on LLMs, retrieval-augmented generation, agents and semantic search.

Isomorphic Labs · London

Contribute to the design of novel large-molecule therapeutics by applying computational and machine learning methods to predict biologics properties such as affinity, developability and immunogenicity from sequence. Work within an interdisciplinary computational sciences team alongside ML and biologics discovery experts, benchmarking models, analysing lab data and shaping data-generation strategies for active learning.

GSK · Stevenage · US$340,500 – US$567,500 pa

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability. Builds and leads a matrix Medicine Development Team spanning clinical development, immunology, manufacturing, regulatory, safety, medical affairs and commercial, and sets the asset strategy within GSK's oncology R&D portfolio.

GSK · Zug, Switzerland · US$340,500 – US$567,500 pa

Leads global development of a cancer vaccine asset from late-stage transition through approval and launch, acting as single point of accountability across major markets. Builds and directs a matrix Medicine Development Team spanning clinical development, immunology/biomarkers, manufacturing, regulatory, safety, medical affairs and commercial, and serves as asset spokesperson to senior governance boards.

Vertex Pharmaceuticals · London

A 12-month industrial placement within an international Medical Affairs team, supporting the planning and execution of medical projects in assigned therapeutic areas. The role involves project management, monthly dashboard reporting, managing external agencies, monitoring budgets for medical education events and advisory boards, and liaising with cross-functional and external stakeholders.

Vertex Pharmaceuticals · London

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

Relation Therapeutics · London

Senior project manager role coordinating a multi-year osteoporosis drug discovery programme across target ID, hit-to-lead, lead optimisation and candidate selection. Involves orchestrating matrixed wet lab, ML, data science and engineering teams plus CROs, managing plans, budgets, risks and governance, and translating scientific objectives into integrated timelines and milestones.

Ipsen · London

Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.

Fortrea · Maidenhead

Monitors clinical trials across the UK under a risk-based model, covering oncology and haematology studies plus neuroscience, cell and gene therapies and other therapeutic areas. Requires at least six months of independent monitoring experience and involves 8+ on-site days per month, working with multiple protocols for biotech and biopharma sponsors.

Danaher · Portsmouth

Responsible for new product development and improvement projects for hardware and disposable devices used in the biotech industry, taking initiatives from spec definition through design, testing and validation to manufacturing transfer. Provides technical leadership on complex engineering challenges, applies 3D CAD design, manages project plans and resources, and reports progress to leadership. On-site role with up to 20% international travel.

Pfizer · New York, United States · US$176,600 – US$294,300 pa

Leads global evidence generation strategy for a rare disease therapy, overseeing HEOR studies such as network meta-analyses, economic models, and patient-reported outcomes. Partners with cross-functional teams and country affiliates to support reimbursement and market access, managing vendors and budgets. Requires deep HTA and health economics expertise within a matrix organization.

Pfizer · Europe - Any Pfizer Site · US$176,600 – US$294,300 pa

Leads global health economics and outcomes research for a rare disease asset, developing evidence generation strategy and HEOR studies such as network meta-analyses, economic models and patient-reported outcomes. Oversees launch deliverables including value dossiers and systematic literature reviews, working with cross-functional and country teams to support reimbursement and patient access.

Nuclera · Cambridge

Formulate, dispense and quality-control reagents for a protein discovery platform, operating lab equipment such as pipettes, centrifuges and UPLC systems. The role covers batch documentation, inventory management via ERP and troubleshooting production deviations, working closely with R&D, QA and Supply Chain in a fast-paced lab environment.