Biotechnology Jobs

• Durham Blackwell Street
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and delivery of real-world evidence and health outcomes studies for oncology assets, managing protocols, budgets, vendors and reporting from concept to publication. Advises medical, market access and commercial teams on payer and HTA evidence needs, and builds relationships with external experts and data partners.

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

Leads clinical development of oncology assets in genitourinary cancers, overseeing Phase 1-3 interventional trials from protocol design through final study report. Provides real-time medical monitoring, safety review with pharmacovigilance, and regulatory document authoring, while building relationships with key external experts. Serves as a core member of the Clinical Matrix Team and contributes to disease area strategy and business development diligence.

• Maidenhead
• Hybrid · 3 days in office
• Director

Leads strategic sourcing and evaluation of late-stage external clinical assets in Immunology, from Phase 2 through marketed drugs, as the senior S&E leader within the Therapy Area Leadership Team. Drives proactive sourcing, cross-functional due diligence, and KOL engagement, partnering with BD to advance high-priority opportunities through negotiation and deal close.

• Stevenage
• Hybrid
• Senior

Hands-on senior role owning the computerised-system lifecycle for GxP systems, from impact and supplier assessments through validation, release, operation and retirement. Authors and executes CSV documentation, performs data integrity and 21 CFR Part 11 assessments, manages change controls and CAPAs, and supports regulatory inspections as a CSV subject matter expert.

SaaS · Cloud

• 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

• Oxford
• On-site
• Mid-level

Perform routine cGMP Quality Control testing using HPLC, UPLC, GC, UV spectroscopy, DLS and Karl Fischer analysis, supporting raw materials, in-process materials, drug substance, product release and stability programs. Coordinate and execute global GMP stability studies, manage sample lifecycles in LabVantage LIMS, trend data statistically, and author protocols and regulatory documentation. The role is 100% onsite at the Harwell facility and involves collaboration with manufacturing, QA, regulatory and external testing partners.

LabVantage · LIMS · Generative AI

• Cambridge
• Hybrid · 3 days in office
• Lead

Designs and builds end-to-end AI and optimisation solutions, including mathematical optimisation, modelling and simulation, for complex pharmaceutical business problems. Works in a global team of AI engineers, data scientists and software developers, visualising model outputs and championing software engineering best practices such as Python, CI/CD and testing.

CPLEX · Gurobi · SCIP +1

• Cambridge
• Hybrid
• Mid-level
• Permanent

Educates and trains clinicians on Masimo monitoring technologies, running product demonstrations, evaluations and deployments alongside account managers across the Eastern UK territory. Requires critical care, NICU, PICU or emergency nursing background and involves around 60% travel with overnight stays.

PowerPoint

• Portsmouth
• On-site
• Senior
• Permanent

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.

• London
• Hybrid
• Lead · manages people

Leads one or more Early Development Asset Teams, owning integrated strategy from candidate nomination through first-in-human trials across preclinical, translational, clinical, regulatory and CMC workstreams. Serves as scientific champion for oncology assets, presenting data and investment recommendations to governance bodies and contributing to in-licensing due diligence.

• London
• Hybrid
• Entry level
• Internship

A 12-month industrial placement within Vertex's International Supply Chain team, supporting commercial supply operations that deliver medicines globally. The student gains hands-on exposure to pharmaceutical supply chain processes, working with experienced colleagues on analytical, data-driven tasks. Based at the Paddington HQ with hybrid or on-site working options.

• London
• Director · manages people
• Permanent

Lead the team behind hybrid on-prem and cloud compute infrastructure, Kubernetes clusters, and scientific compute environments supporting ML and drug discovery. Own platform strategy, CI/CD maturity, observability, and security controls for sensitive patient-derived data, reporting to the VP of Engineering.

Kubernetes · Kubeflow · GPU Compute +3

• London
• On-site
• Junior

Hands-on lab role in a biology team, running experiments across process development, product testing and platform R&D, maintaining iPSC lines and differentiation cultures, and sharing lab operations duties. Data generated feeds directly into how processes and platforms evolve, with structured training from SOP-based work towards independent execution.

Excel · GraphPad Prism

• Reading
• Remote
• Lead

Provides strategic medical and scientific subject matter expertise in hematology-oncology, advising internal stakeholders on protocol design, clinical development plans and proposals, and supporting client bid-defense meetings. Acts as an internal and external consultant across the research and development lifecycle, coaching project teams and collaborating with business development and operations. Greater independence is expected over time under the therapeutic area head.

• Cambridge
• Hybrid · 3 days in office
• Lead · manages people
• Permanent

Accountable to the Global Clinical Head for an indication-aligned cluster of late-phase Respiratory and Immunology studies, supervising Global Development Medical Directors and Scientist Directors. Leads cross-functional design, conduct, monitoring and data interpretation, represents the program at health authority interactions, and co-leads publication strategy.