Latest IT Recruitment Jobs

Site Shift Manager

This role involves leading 24/7 manufacturing operations outside core hours at GSK’s Barnard Castle site, ensuring safety, compliance, and supply chain continuity. The Site Shift Manager acts as the primary on-site leader during shifts, coordinating production, managing incidents, and aligning cross-functional teams including manufacturing, quality, and engineering. Emphasis is placed on real-time decision-making, audit readiness, and continuous improvement in a regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Operations NPI Technologist

This role involves leading the integration of new equipment, processes, and technologies into sterile manufacturing operations, ensuring compliance, safety, and minimal disruption to supply. The technologist will work across project lifecycles—from design and validation to handover—providing technical leadership and operational readiness support. Collaboration with engineering, quality, and digital manufacturing teams is key to deploying capital projects and new product introductions in a GMP-regulated environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Head of AI & Agentic Platform Engineering

Leads the design and operation of Pfizer's core AI and agentic platform infrastructure, enabling enterprise-wide AI workloads across R&D, Commercial, and other functions. Focuses on building scalable, secure, and governed systems for LLM serving, agent orchestration, MLOps, and runtime observability. The role is central to accelerating AI deployment velocity while ensuring compliance, especially in regulated environments.

Pfizer US$300,100 – US$500,100 pa

Hybrid Permanent

Head of AI & Agentic Platform Engineering

This role leads the development and operation of Pfizer's core AI and agentic platform infrastructure, enabling enterprise-wide AI workloads across R&D, Commercial, and other functions. The leader will architect a scalable, secure, and governed platform supporting LLM gateways, agent orchestration, model serving, and production observability, with a focus on enabling autonomous AI systems. The platform must support both current AI tools and future agentic systems requiring stateful execution, tool calling, and cross-agent coordination.

Pfizer US$300,100 – US$500,100 pa

Hybrid Permanent

Senior Scientist – AI and Computational Tools, Oncology R&D (12-Month

This role involves designing and deploying AI-powered tools and workflows for oncology research, building robust data infrastructure, and mentoring colleagues in computational methods. The Senior Scientist will work closely with wet-lab scientists, data science teams, and R&D IT to translate experimental data into scalable, reproducible systems.

AstraZeneca Cambridge, United Kingdom

On-site Contract

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Principal Programmer / Analyst

This role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering quality assurance and innovation.

GSK

Hybrid Permanent

Principal Scientist/Senior Principal Scientist – Statistical Genetics

This role involves applying advanced statistical and computational methods to large-scale genetic, genomic, and clinical datasets to generate translational insights for drug discovery and development. The scientist will interpret complex data to uncover causal disease mechanisms, support target and biomarker identification, and enable precision medicine approaches across multiple therapeutic areas. Collaboration with multidisciplinary teams and external partners is key, along with contributing to scientific innovation through publications and methodological advancements.

GSK

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external drug product manufacturing, coordinating between GSK and Contract Manufacturing Organisations (CMOs) to ensure timely and compliant delivery. The specialist will drive project schedules, mitigate risks, align cross-functional teams, and maintain governance across the supply chain, particularly for sterile drug products like monoclonal antibodies and vaccines. A key focus is ensuring technical knowledge retention and operational readiness for new suppliers or assets.

GSK United Kingdom €69,600 – €116,000 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and data foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance. The Associate Director will lead digital integration, dashboard governance, and process improvements, acting as a bridge between business and technology teams to enhance efficiency and regulatory adherence in clinical operations.

GSK United States US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data integrity, system governance, and digital transformation. The individual will own the data and dashboard ecosystem, act as Business System Owner for key platforms like IdeaPoint and Veeva, and ensure compliance with regulatory requirements such as Transfer of Value. They will bridge business and technology to drive process improvements, enable resource planning, and enhance data transparency across clinical operations.

GSK £154,275 – £257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies program. The Associate Director will lead data governance, system ownership, and digital integration efforts, ensuring data integrity, compliance, and efficiency across platforms like Veeva and IdeaPoint. The position acts as a bridge between business and technology, driving process improvements and digital transformation in a regulated clinical environment.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads the operational and digital foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance across platforms like Veeva and IdeaPoint. The individual will drive process improvements, support regulatory reporting such as Transfer of Value, and act as a bridge between business and technology teams to enhance efficiency and scalability in clinical operations.

GSK US$154,275 – US$257,125 pa

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

The role involves managing technology transfer projects for external manufacturing of drug products, coordinating between GSK and Contract Manufacturing Organisations (CMOs). The specialist ensures timely delivery of critical path activities, aligns internal and external stakeholders, and maintains governance across procurement, quality, technical, and supply functions, particularly for sterile drug products like monoclonal antibodies and vaccines.

GSK €69,600 – €116,000 pa

Hybrid Permanent

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The specialist provides expert guidance on safety profiling, candidate selection, and translational planning, while mentoring teams and shaping regulatory narratives. They work cross-functionally to ensure robust safety evaluation for small molecules and biologics through clinical and post-market stages.

GSK £224,400 – £374,000 pa

On-site Permanent