Biotechnology Jobs

GSK · London

Builds and maintains financial and operational models, forecasts and dashboards that guide R&D portfolio and investment decisions, including NPV/rNPV, scenario and sensitivity analysis and Monte Carlo simulation. Works with the Head of Data Science and the Finance Portfolio Analytics Manager, turning scientific, clinical, financial and operational data into clear outputs for review discussions.

GSK · USA - Pennsylvania - Upper Providence

Builds and maintains financial and valuation models (NPV/rNPV, scenario and sensitivity analysis) and portfolio forecasts, metrics and KPI dashboards for R&D investment decisions. Runs probabilistic and Monte Carlo simulations, cleans data from scientific, clinical, financial and operational sources, and prepares decision materials for portfolio reviews. Works with the Head of Data Science and the Finance Portfolio Analytics Manager in a hybrid, high-visibility team.

CSL · Maidenhead

Leads an integrated quality assurance organisation covering Good Clinical Practice and Good Pharmacovigilance Practice, reporting to the Head of Global R&D Quality. Sets strategy, operating model and standards for risk-based QA oversight from trial design through close-out, including clinical safety interfaces, inspection readiness and CAPA frameworks. Hybrid role with global scope and international travel.

CSL · Waltham, United States

Leads an integrated quality assurance organisation covering Good Clinical Practice and Good Pharmacovigilance Practice, reporting to the Head of Global R&D Quality. Sets strategy, operating model and standards for risk-based QA oversight from trial design through close-out, including inspection readiness, CAPAs and clinical safety interfaces such as SAE reconciliation and expedited reporting. Hybrid role with global team leadership and international travel.

Recursion · New York, United States · US$151,800 – US$220,660 pa

Integrate phenomics, transcriptomics, genomics and proteomics data to nominate novel targets and validate immunology and inflammation disease biology, piloting new methods for target discovery and early patient population hypotheses. Partner cross-functionally with biologists, chemists, data scientists and engineers to build data packages that drive program milestones and investment decisions.

Recursion · New York, United States · US$151,800 – US$220,660 pa

Integrates phenomics, transcriptomics, genomics and proteomics data to nominate and validate oncology targets and define precision oncology patient strategies. Partners cross-functionally with biologists, chemists, engineers and translational experts to build target data packages and pilot novel discovery methods, including agentic target packages and mechanism-of-action work.

AstraZeneca · London

Finance lead for a designated disease area with full P&L ownership across UK & Ireland in-line and pipeline assets. Drives strategic planning, budgeting, monthly forecasting and pricing/reimbursement business cases, applying AI and advanced analytics, while partnering Commercial, Medical, Market Access and Global Finance. Office-based in London with at least 60% attendance.

Newton Colmore · Cambridge

Lead the design and development of next-generation drug delivery devices, guiding multidisciplinary teams of engineers, scientists and designers from early-stage concepts through to manufacturable solutions. The role blends hands-on R&D work — concept generation, prototyping, experimental design, verification planning and risk management — with client-facing consultancy, programme leadership and mentoring of junior colleagues.

Moderna · London

Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.

SRG · Loughborough · £14 – £15 ph

Perform analytical testing for batch release, stability studies and complaint investigations in a GMP/GLP-regulated pharmaceutical lab, using techniques such as HPLC and UV spectroscopy. Support OOS/OOT investigations, maintain Good Documentation Practices, review and issue GMP documentation, and help with calibration and equipment maintenance. A 12-month temp contract within a cross-functional QC team.

Autolus · London

Designs end-to-end data solutions spanning data integration, data warehousing, master data management, governance and analytics for a biopharmaceutical company. Translates business requirements into data models, data flows and integration patterns, and leads architecture and design reviews across enterprise applications and cloud data platforms.

Vertex Pharmaceuticals · London

Leads regional or global regulatory strategy for development programs and marketed products, serving as a regulatory lead and primary contact with health authorities. Manages preparation, submission and approval of regulatory applications, advises teams on approval pathways and expedited routes, and monitors regulatory intelligence to inform strategy.

Newton Colmore · Cambridge

Lead the design and development of next-generation drug delivery devices, guiding multidisciplinary teams of engineers, scientists and designers from early-stage concepts through to manufacturable solutions. The role blends hands-on R&D work — concept generation, prototyping, verification planning and risk management — with client-facing consultancy, programme leadership and mentoring of junior colleagues.

Moderna · London

Shape global CMC regulatory strategy for an innovative mRNA medicines portfolio, driving international submissions and health authority interactions. Prepare and review CMC sections of regulatory filings, advise Manufacturing and Quality teams, and oversee multiple development programs. An individual contributor role with global reach, working alongside teams using digital and Generative AI tools.

Genomics · London

Client-facing programme manager role setting up and embedding a multidisciplinary delivery team around a major pharma partnership, running the integrated delivery plan, milestones, dependencies, risks and resourcing. Coordinates across Science, Data, Engineering, Finance, Legal and People stakeholders, running status meetings, reporting and escalations with the partner. Structured as a six-month engagement with an immediate start.