Biotechnology Jobs

• Oxford
• On-site
• Mid-level · manages people
• Permanent

Lead the governance, lifecycle management and regulatory compliance of physical assets across a growing scientific and engineering campus. Establish and improve an ISO 55000-aligned Asset Management System, driving predictive and condition-based maintenance, whole-life cost modelling and risk-based investment planning. Manages a team and specialist suppliers; explicitly not a facilities or property operations role.

• UK - Hertfordshire - Ware RD
• Director

Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, leading protocol and study document development, serving as medical monitor for Phase 1–4 trials, and interpreting efficacy, safety and biomarker data. Works within cross-functional global study teams and the Clinical Matrix Team, with informal coaching of less experienced clinical scientists and no formal line management.

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to analysis-ready, audit-ready data. Works in a matrix with strategy, biomarker, clinical operations, data management, regulatory, quality and procurement teams, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO · Central Labs · Reference Labs

• 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

• Maidenhead
• Hybrid
• Senior · manages people
• Permanent

Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.

RAVE · EDC

• Cambridge
• Hybrid · 3 days in office
• Director

Provides medical and scientific leadership across late-stage respiratory and immunology clinical programs, from Phase IIb to Phase IV. Involves designing, executing and interpreting pivotal trials, medical monitoring, regulatory document input and building relationships with external scientific experts in an international team.

• London
• Hybrid · 3 days in office
• Senior

Operating Partner supporting VPs of AI on high-priority strategic initiatives, acting as a trusted advisor and operational force-multiplier. The role involves translating complex machine learning concepts into executive communications, driving cross-functional alignment without line authority, and unblocking inefficiencies across research, engineering, product and operations in a fast-scaling environment.

AlphaFold

• London
• Hybrid
• Mid-level

Drives clinical supply forecasting and IMP budgeting for global trials, translating study protocols and recruitment projections into forecasting tools and monitoring deviations over 3-12 month horizons. Coordinates cross-functional IMP estimation and risk assessment meetings, aligning manufacturing, packaging and distribution to prevent stock-outs, while leading continuous improvement in a matrixed environment.

RTSM · Excel

• Maidenhead
• Hybrid · 3 days in office
• Director · manages people

Leads scientific safety assessments for assigned medicinal products, partnering with Medical Safety Officers to prepare analyses and evaluations for regulatory compliance. Supports Safety Management Teams, conducts proactive safety data reviews, and serves as product point of contact, with hybrid working requiring three days on site.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• 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

• Maidenhead
• Mid-level · manages people

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects for content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves guiding cross-functional teams, peer review and maintaining knowledge of ICH and regulatory guidelines.

• Madrid, Spain
• Hybrid
• Senior

Builds, trains, deploys and maintains AI/ML models and automation tools for supply chain master data within Pfizer's Supply Planning Data Intelligence group. Work spans optimization algorithms, predictive models, generative AI/NLP, and autonomous data agents integrated with planning systems like Kinaxis, owning solutions from development through production handover.

scikit-learn · pandas · TensorFlow +7

• 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.

• Oxford
• On-site
• Mid-level

Owns product management for ONI's kits and integrated workflows, including the Discovery Kit, EV Profiler and LNP Profiler, ensuring sample prep, fluid handling, imaging, analysis and reporting software operate as one system. Acts as connective tissue between software, hardware, bioware, support and field teams, driving reproducibility, adoption and roadmap across UK and US teams.

Nanoimager · Aplo Platform · Aplo Flow +5

• Cambridge
• Director · manages people

Leads a team of medical writers and oversees strategic planning and drafting of complex regulatory submissions at the therapeutic area or portfolio level. Acts as subject matter expert, driving document strategy with cross-functional teams across Regulatory Affairs, Clinical Research and Clinical Data Science, plus process improvement and training initiatives.

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