Biotechnology Jobs

• London
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Leads the global development of a medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and directs a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving strategy, governance and go/no-go decisions. Hybrid role with at least two days per week on-site.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$266,250 – US$443,750 pa
• Director · manages people

Strategically leads global development of an oncology medicine from clinical Proof of Concept to approval in first major markets, acting as single point of accountability. Builds and leads a matrixed Medicine Development Team spanning clinical, medical, commercial and manufacturing, driving evidence packages, governance decisions and lifecycle plans.

• Oxford
• Hybrid
• Senior

Builds and operates a cloud platform for scientific computing, including full-sized GPU clusters, resilient compute, network and storage. Implements auditable CI/CD and GitOps pipelines, Policy-as-Code governance with Kyverno, and foundational monitoring, alerting and SLOs. Partners with research and data teams to deliver self-service capabilities for workloads from Python notebooks to distributed clusters.

Kyverno · YAML

• Oxford
• Hybrid
• Mid-level
• Permanent

Builds the data layer for an autonomous lab platform, ingesting high-frequency video, sensor telemetry and robot state across an edge-to-cloud stack using MQTT, Kafka and streaming APIs. Turns raw streams into structured database transactions and a traceable knowledge graph, and shapes data into model-ready formats for vision-language-action and world models alongside AI and robotics researchers.

MQTT · Kafka · HLS

• Home Worker
• Remote
• £49,140 – £91,260 pa
• Lead · manages people

Leads statistical programming strategy for clinical trials and programs, acting as Trial, Lead or Program Programmer and coordinating internal and external teams. Develops and validates CDISC-compliant datasets and outputs for regulatory submissions, using R, SAS or Python, Git-based version control and reproducible workflows. Also shapes standards, templates and governance across studies.

R Shiny · Tidyverse · Git +2

• London
• Hybrid · 3 days in office
• Mid-level

Join a newly formed Scheduling team to own and extend systems orchestrating compute allocation for complex ML workloads on Kubernetes. You'll design scheduling policies like gang scheduling and topology-aware placement, build custom Kubernetes controllers and CRDs, and optimize GPU/TPU utilization while partnering with ML researchers on reliability and SLOs.

Kubernetes · Kueue · Volcano +4

• Groton, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead

Leads the strategy, design and lifecycle management of digital clinical supply chain systems for Global Clinical Supply, working with product managers and business SMEs on a 3-5 year roadmap. Drives process and technology integration, system modernisation and retirement, and enterprise-level portfolio prioritisation while reporting progress to senior management. Hybrid role with up to 15% travel.

• Reading
• Mid-level · manages people

Leads end-to-end delivery of regional and global clinical trials embedded within a sponsor's team, managing timelines, budgets, risk and cross-functional groups. Also supports bid defence presentations, vendor management and financial forecasting, mentoring less experienced project team members.

IQVIA

• Cardiff
• Lead

Develops and drives the long-term global operations and supply chain footprint strategy for the Discovery & Medical business, translating business strategy into network and footprint roadmaps across manufacturing, sourcing, warehousing, capacity, localization and productivity. Leads business-case development, CapEx/OpEx planning and governance for cross-functional footprint initiatives, with up to 30% international travel.

Danaher Business System · Automation · Additive Manufacturing

• Andover, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead · manages people

Lead the digital transformation of Pfizer's clinical supply chain systems, overseeing the full lifecycle from concept to decommissioning. Define multi-year product strategies, drive process and technology integration, and guide cross-functional teams to ensure regulatory compliance and efficient delivery of investigational products worldwide.

• High Wycombe
• Hybrid · 3 days in office
• Entry level
• Internship

A 12-week summer internship in EMEA Global Regulatory Affairs within the Oncology therapeutic area, working on a hybrid model with three days on site. Interns join a global matrixed team supporting clinical strategies and Phase I-III oncology studies, contributing to regulatory strategy, clinical trial applications and product registration activities, with a mentor, cross-functional team meetings and a research poster presented at a company-wide symposium.

Microsoft Outlook · Microsoft Excel · Microsoft PowerPoint +5

• Oxford
• On-site
• Temporary

Serve as engineering owner for GMP manufacturing equipment at Moderna's Harwell facility, supporting the Norwood (MA) network. Provide hands-on floor support, troubleshoot complex mechanical and process issues, lead CAPAs and change controls, and drive continuous improvement and tech transfer for mRNA production. Requires close cross-functional work with equipment SMEs and end users.

TMIX · Single Use Mixers · Buffer Prep Vessels +4

• 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

• United Kingdom
• Remote
• Senior
• Permanent

Provides clinical quality oversight and a single point of Quality contact for client study teams, partnering with Clinical Operations and Pharmacovigilance to identify, assess and mitigate risks to participant safety and reporting compliance. Co-chairs Joint Quality Councils, analyses QA metrics and audit/inspection trends, and drives quality risk management across a portfolio. Fully remote role with up to 25% travel.

• United Kingdom
• Remote
• Lead

Supports central comparator sourcing for clinical trials on a client-dedicated FSP team, covering market intelligence, sourcing recommendations, and purchase order execution across EMEA. Acts as an SME on the external comparator landscape, advising on regional and central/local sourcing strategy while escalating quality or temperature issues to the client.