Latest Technology Jobs

Postdoctoral Research Fellow (Jamali Lab) - Generative Biology Institute

Design and develop generative protein models that capture enzyme dynamics and function, with a focus on catalysis through motion. Analyze complex datasets and collaborate with interdisciplinary teams to evolve designs in vivo. Contribute to high-impact research publication and translation within a cutting-edge synthetic biology environment.

Ellison Institute of Technology Oxford, United Kingdom £40,000 pa

On-site

Fluidic System Engineer - Pathogen

Design and develop microfluidic systems for a point-of-care diagnostic device that enables metagenomic sequencing through a cartridge-based interface. Work closely with cross-functional teams to integrate microfluidics with instrumentation, electronics, and firmware, focusing on robustness, automation compatibility, and real-world performance. Conduct prototyping, testing, and validation using techniques like soft lithography and rapid prototyping to advance decentralized infectious disease diagnostics.

Ellison Institute of Technology Oxford, United Kingdom

On-site

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

Provides medical and scientific leadership in safety evaluation and risk management for GSK’s clinical and post-marketing assets. Key responsibilities include signal detection, safety oversight, regulatory reporting, and contributing to global pharmacovigilance strategy. Works cross-functionally to ensure patient safety and compliance with international regulations.

GSK €87,000 – €145,000 pa

Hybrid Permanent

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

This role involves providing medical and scientific leadership in the safety evaluation and risk management of GSK’s clinical and post-marketing pharmaceutical assets. The Associate Medical Director will lead signal detection, benefit-risk assessment, and pharmacovigilance strategy, ensuring robust safety oversight across global development programs. Working within a cross-functional matrix, the individual will influence safety governance, contribute to regulatory submissions, and drive evidence-based decisions to protect patient safety.

GSK €87,000 – €145,000 pa

Hybrid Permanent

Innovation, Data & Analytics Team, AI/ML Engineer (Agentic Systems)

Own the orchestration layer and agent architecture behind the Innovation, Data & Analytics team's AI-based workflows, building and hardening agentic systems that translate analytical methodology into reliable production tools.

Pfizer

Sr. Manager, Operational Strategy Lead

Leads the development and execution of end-to-end clinical supply operational strategies for Pfizer’s global clinical programs, focusing on packaging, labeling, and distribution. Works cross-functionally with supply chain, clinical research, and quality teams to ensure compliant, timely delivery of clinical supplies while driving continuous improvement and digital transformation initiatives. Plays a key role in risk management, cost forecasting, and strategic planning to support patient-centric clinical trials.

Pfizer Sandwich, United Kingdom

Senior Manager, Government Affairs – UK

This role involves shaping and executing Moderna’s Government Affairs strategy across the UK, with a focus on enabling innovative mRNA-based respiratory vaccines through policy engagement. The individual will build relationships with government, Parliament, and healthcare stakeholders, translate political and policy trends into strategic positions, and leverage AI tools to enhance policy intelligence. Collaboration across internal teams and external partners is key to influencing public policy and supporting Moderna’s mission in a fast-paced, innovation-driven environment.

Moderna London, United Kingdom

Facilities Engineering Manager

This role involves providing technical leadership for facility and utility systems at Moderna’s new biotech site in Harwell, Oxford. The Facilities Engineering Manager will oversee maintenance, vendor performance, and engineering projects across R&D and manufacturing environments, ensuring compliance and operational reliability. The position emphasizes continuous improvement, digital tool integration, and collaboration with global teams in a GMP-regulated setting.

Moderna Oxford, United Kingdom

On-site Permanent

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Senior Scientist Oncology Research

Conduct laboratory-based research to support immune-oncology drug discovery, focusing on developing and analysing in-vitro and ex-vivo assays to evaluate candidate therapeutics. Investigate mechanisms of action in tumour immunology using advanced immunological techniques and contribute to target validation. Work within a collaborative team environment in Cambridge, integrating scientific expertise with emerging data and technologies.

AstraZeneca Cambridge, United Kingdom

Contract

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Executive Director, Strategy, Oncology R&D

This role involves leading the global Oncology R&D strategy at AstraZeneca, shaping high-impact therapeutic area strategies by integrating clinical, scientific, and commercial insights. The individual will advise senior leadership, drive portfolio optimization, and influence strategic investment decisions with a focus on patient outcomes and innovation. It requires deep scientific and strategic expertise, strong analytical rigor, and the ability to lead cross-functionally in a complex, matrixed environment.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Head, PV and Regulatory QA

This role leads the global quality and compliance function for pharmacovigilance (PV) systems, ensuring adherence to international regulations and internal standards across clinical safety, regulatory affairs, and medical affairs. The position combines strategic oversight with hands-on operational leadership, including audit strategy, inspection readiness, deviation and CAPA management, and cross-functional GxP guidance. It requires deep technical expertise in PV processes and strong leadership to drive quality across global teams and third-party vendors.

CSL

Head, PV and Regulatory QA

Leads global pharmacovigilance and regulatory quality assurance, ensuring compliance with GVP, ICH, and regulatory standards across clinical safety, medical affairs, and regulatory affairs. Designs audit strategies, manages inspections, and oversees deviation management, CAPA, and change control systems. Provides cross-functional GxP expertise and drives continuous improvement in PV quality systems.

CSL

GCP Compliance Director (EMEA Hub)

This role leads Good Clinical Practice (GCP) compliance across Novartis' EMEA clinical operations, ensuring trials meet regulatory, quality, and ethical standards. The director oversees audits, inspections, and compliance events, while developing a high-performing team and driving risk mitigation. They will partner with global clinical and quality leaders to strengthen inspection readiness and operational excellence in a hybrid working environment.

Novartis London, United Kingdom £83,510 – £155,090 pa