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.

• 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

• Mississauga, Canada
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director

Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for genitourinary studies. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, investigator and KEE engagement, and regulatory interactions. May guide other physicians on complex multi-study programmes.

AI

• London
• Hybrid · 2–3 days in office
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within a clinical programme team, leading medical monitoring and safety oversight for oncology studies and interpreting clinical and safety data. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with a focus on GI oncology. Requires an on-site office presence two to three days a week.

AI-enabled insights

• Swindon
• On-site
• Lead · manages people

Operates and sets up bulk formulation, filling, inspection and packing lines for sterile and non-sterile pharmaceuticals, following SOPs, BMRs and cGMP in a cleanroom environment. Performs CIP/SIP, autoclave and airlock operations, equipment monitoring and documentation, and provides team leadership on night shifts. Distinct for its aseptic manufacturing focus, hazardous materials handling and supervisory duties.

SAP · HMI · EDMS

• United Kingdom
• Remote
• Senior

Clinical Research Associate role within PPD's Functional Service Provider division, dedicated to a client and embedded in multi-national project teams. You perform and coordinate all aspects of clinical monitoring, conducting monitoring activities independently across challenging projects. Requires ICH-GCP, EU and FDA knowledge, with award-winning training provided.

• Harrow
• Remote
• Mid-level

Independently leads statistical aspects of low-to-moderate complexity clinical trials, developing complex analysis strategies and executing them with SAS or R. Reviews analysis datasets, quality-controls statistical deliverables, and contributes to trial design, analysis plans, and regulatory submissions. Works within global cross-functional teams, liaising with clients on data analysis, scope, and budget.

SAS · R

• Oxford
• Hybrid · 3–4 days in office
• Senior
• Permanent

Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.

Thermo Watson LIMS · Watson LIMS · LabVantage eLBN +1

• Maidenhead
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs/FSPs and contributes to governance and development-plan decisions across therapeutic areas.

SAS · R

• Breda, Netherlands
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full scope of statistical contribution to a clinical development programme, defining statistical strategy and methodologies for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with authorities such as FDA, EMA and PMDA, and manages outsourcing or internal statistical programmers. Two positions support multiple therapeutic areas.

SAS · R

• London
• Hybrid
• £56,511 – £104,949 pa
• Mid-level

Lead the development and maintenance of global labelling documents for neuroscience medicines, translating clinical and safety data into compliant product information. Facilitate cross-functional discussions, support Health Authority responses, and ensure timely implementation of labelling changes across global and major markets.

• London
• Hybrid
• £63,917 – £118,703 pa
• Director

Acts as a QA liaison between clinical trial teams and third parties, providing expert support through due diligence, qualification, governance and ongoing monitoring. Focuses on technology-enabled vendors such as digital health tools, medical devices and AI, covering risk assessment, audit support, inspection readiness and escalation of quality issues.

DHT · SaMD · SaaS +1

• Cambridge
• £37,694 – £46,049 pa
• Entry level
• Contract

Conducts molecular virology research on viral cross-species transmission, using cell culture, molecular cloning, viral reverse genetics and functional infection assays. Plans and analyses experiments, maintains records and contributes to manuscripts within a collaborative team at CITIID. Fixed-term for one year in the first instance.

Viral Reverse Genetics · Small Animal Models

• United Kingdom
• Contract

Shape and drive strategic medical affairs initiatives in the Ophthalmology therapy area, working locally and globally within Roche UK's Medical Affairs Chapter. Involves data and insight generation, scientific partnerships, medical education, and mentoring peers while engaging the clinical community.