Latest IT Recruitment Jobs

Steriles Standards Manager

Leads the development and enforcement of operational standards for sterile manufacturing, ensuring compliance with regulatory requirements and driving continuous improvement. Works cross-functionally with quality, engineering, and operations teams to standardize processes, support audit readiness, and strengthen control in aseptic environments. Focuses on reducing variability, improving compliance, and coaching teams in a highly regulated pharmaceutical setting.

GSK Barnard Castle, United Kingdom

On-site Permanent

Deviation Owner

This role involves leading the investigation and resolution of manufacturing deviations in a GMP-regulated environment, ensuring compliance and product quality. The Deviation Owner will coordinate root cause analyses, drive corrective actions, and work across quality, production, and engineering teams to prevent recurrence. Emphasis is placed on data-driven problem solving, governance of deviation processes, and continuous improvement through structured methodologies like DMA/IC.

GSK Barnard Castle, United Kingdom

On-site Permanent

Senior Director, Head of AI for Clinical Development, Early BPRD

This role involves leading the development and application of AI in early phase clinical trials for AstraZeneca, focusing on Phase I/II programs. You will build and manage a team of AI researchers and engineers, develop reusable AI methods, and collaborate with domain experts to improve clinical trial design and decision-making.

AstraZeneca Cambridge, United Kingdom

On-site 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 execution across R&D, Commercial, and other functions. The leader is responsible for building a scalable, secure, and governed platform that supports both traditional ML workloads and next-generation autonomous AI agents, with a focus on stateful agent orchestration, low-latency inference, and full lifecycle governance. The platform enables rapid experimentation, deployment, and monitoring of AI systems in a highly regulated pharmaceutical environment.

Pfizer US$300,100 – US$500,100 pa

Hybrid Permanent Clearance Required

Head of AI & Agentic Platform Engineering

Leads the development and operation of Pfizer's core AI and agentic systems infrastructure, enabling enterprise-wide AI deployment with a focus on scalability, governance, and speed. The role involves building platform layers for LLM serving, agent orchestration, MLOps, and runtime security, ensuring compliance in a regulated pharmaceutical environment. The platform supports autonomous AI agents across R&D, Commercial, and Supply functions, requiring stateful process management, tool integration, and production-grade observability.

Pfizer US$270,100 – US$450,100 pa

Hybrid Permanent

Business Insights Manager or Secondment)

The Business Insights Manager will analyze data from various sources, including sales and market activity, to develop actionable recommendations that support AstraZeneca’s strategic goals. Key responsibilities include leading market research projects, forecasting, and collaborating with teams in Marketing, Finance, and Market Access, specifically focusing on the Cardio-Renal therapy area.

AstraZeneca London, United Kingdom

Hybrid Contract

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 position involves mentoring teams, shaping translational plans, and providing expert input on safety profiling and candidate selection. It plays a key part in regulatory strategy and cross-functional leadership within a global biopharma environment.

GSK £224,400 – £374,000 pa

Hybrid Permanent

Director, Global RWE-HO, Oncology

Leads the planning, design, and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across the product lifecycle. Collaborates with cross-functional teams to generate robust evidence for regulatory, reimbursement, and market access decisions. Focuses on translating clinical and economic value into impactful data for payers, providers, and patients.

GSK United States

Hybrid Permanent

Director, Global RWE-HO, Oncology

This role involves leading the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across their lifecycle. The Director will develop robust data generation plans, align evidence with regulatory and payer requirements, and collaborate with cross-functional teams and external experts to ensure impactful evidence for market access and patient outcomes. The position plays a strategic role in shaping value propositions through scientifically credible research in a global, matrix environment.

GSK

Hybrid Permanent

Director, Global RWE-HO, Oncology

Leads the design and execution of real-world evidence and health outcomes studies to support oncology assets, ensuring robust data generation for regulatory, reimbursement, and market access decisions. Collaborates across medical, commercial, and R&D teams to align evidence strategies with global customer needs and health technology assessment requirements. Engages with external experts and internal stakeholders to deliver high-impact scientific research throughout the product lifecycle.

GSK

Hybrid Permanent

Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through commercial manufacturing. The Molecule Steward ensures product quality, manufacturability, and regulatory compliance by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives across the global supply chain.

GSK United States

Hybrid Permanent

Product Owner, Clinical Trial Site Management

This role involves leading AI-first product development for clinical trial site management systems at GSK, focusing on transforming how trials are conducted from feasibility through close-out. The Product Owner will drive strategy, adoption, and innovation across site-facing and internal operational platforms, using AI to enhance processes like contracting, budgeting, and monitoring. The role emphasizes responsible AI integration in a regulated GxP environment, with strong stakeholder collaboration across R&D operations and technology teams.

GSK United Kingdom

Hybrid Permanent

Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. The Director will guide cross-functional teams in designing and validating digital biomarkers, collaborating with external partners, and enhancing the efficiency and patient-centricity of GSK's clinical trials.

GSK

On-site Permanent

Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. The Director will guide cross-functional teams in designing digital biomarkers, endpoints, and measures, and collaborate with external partners to enhance clinical trial efficiency and patient-centric outcomes.

GSK Exeter, EX4 4HD, United Kingdom

On-site Permanent

Principal Medical Writer

The Principal Medical Writer will author and deliver high-quality clinical regulatory documents, lead cross-functional teams in developing clinical dossier documents for global regulatory submissions, and manage complex writing projects. They will interpret complex clinical and statistical information, ensuring compliance with GSK standards and regulatory requirements.

GSK

Hybrid Permanent