Jobs at GSK

Lead product strategy and delivery for AI-enabled regulatory intelligence and health-authority engagement platforms. Own vision, roadmap, AI/NLP-enabled analytics, compliance (GxP), agile delivery, budgets, vendors, and stakeholder influence across R&D and regulatory functions.

Design, build, validate and document programming solutions to transform clinical and real-world data into SDTM/ADaM datasets and TFL outputs. Collaborate with statisticians and cross-functional teams, perform code reviews and quality checks, ensure compliance with GxP/ICH standards, and help introduce programming best practices and tools within an agile delivery environment.

Lead digital products for regulatory intelligence and health-authority engagement: set vision and roadmap, connect portfolios, co-design compliant user journeys, champion AI-first solutions, deliver increments end-to-end, embed GxP/privacy/AI governance, and mentor product teams to improve regulatory interactions and transparency.

The SERM Scientific Director leads pharmacovigilance and risk management strategies, ensuring safety evaluation of GSK assets and compliance with regulatory standards. Responsibilities include managing safety reviews, cross-functional team leadership, and communicating safety issues to senior management and regulatory bodies.

Lead CMC regulatory strategy for development and lifecycle activities. Coordinate and author CMC submission content, manage complex projects and inspections support, advise on global regulatory requirements, mitigate submission risks, and influence regulatory decisions across cross-functional teams to ensure timely product access and uninterrupted supply.

Perform sample analysis using various analytical techniques, generate and check data to regulatory and ALCOA+ standards, maintain and calibrate lab equipment, investigate OOS/atypical results, support method transfers and validation, apply statistical methods, improve lab processes, and train or support colleagues while ensuring GMP, EHS and 5S compliance.

Lead global CMC regulatory strategy for small molecule medicines, represent CMC on cross-functional teams, identify regulatory risks and mitigation plans, support development and uninterrupted supply, mentor colleagues and manage a small team, and improve regulatory processes to enable approvals and lifecycle management.

Lead the UK commercial operations team for ViiV Healthcare, owning marketing strategy, commercial planning, forecasting, KPI dashboards, cross-functional projects, launch readiness, compliance, and people development to optimise HIV portfolio performance.

Perform GMP-compliant product testing and analysis for oral and solid dose products, support lab operations to maintain supply, follow procedures, ensure EHS compliance, collaborate across teams, troubleshoot and drive continuous improvement.

The VIDRU Business Programs Strategy Director leads and manages enterprise-wide programs to ensure strategic initiatives deliver measurable value, synthesizing insights and facilitating cross-functional collaboration.

Lead strategic planning and scheduling for large capital projects, enforce schedule governance, run quantitative schedule risk (Monte Carlo), manage schedule tools, mentor planning staff, integrate planning with cost/risk/contracts, and present schedule performance to senior leadership.

Lead global overland (road freight) category strategy, analyze spend to identify savings, benchmark market rates, negotiate supplier agreements, govern 4PL/3PL models, manage tenders, track savings, drive sustainability and supplier performance, and support TPRM and cross-functional implementation.

The role involves designing, implementing, and delivering AI/ML solutions, developing machine learning models for scientific tasks, and collaborating with experts for data processes.

Lead late-stage drug product development for small molecule parenteral (LAIs) and oligonucleotide modalities. Guide cross-functional teams on formulation, fill-finish, process development, scale-up, technology transfer, and regulatory CMC deliverables to ensure clinical and commercial supply readiness and product quality.

Lead planning and delivery of complex, multi-site supply chain programmes (network exits, lifecycle management, product launches, integrations). Define scope, mobilise cross-functional teams, manage budgets, risks, governance and stakeholder communications to deliver strategic supply chain objectives across GSK.

Lead development and oversight of advanced demand and supply models for high-value clinical trials, optimize clinical supply strategies, integrate complex data sources, validate models, produce visualizations and recommendations, align cross-functionally, and drive portfolio-level forecasting, risk mitigation and value realization.

Manage and improve stability data for small molecule studies: create and maintain study protocols, collate and analyse datasets, produce summaries and visualisations, manage sample schedules, support audits/inspections, collaborate with internal and external teams, and drive digital tool adoption and process improvements.

Design, build, and operate a hybrid on‑prem/cloud compute platform for interactive and large-scale batch computing. Develop CI/CD-driven containerized environments, optimize application performance at scale, consult scientists on scalability, ensure observability, testing, documentation, and mentor team members to drive platform adoption and reliability.

Designs, builds, and operates hybrid on-prem/cloud compute platforms, toolchains, CI/CD, and workflows for interactive and large-scale batch scientific computing. Consults scientists on scalability and performance, produces well-engineered software with tests and docs, ensures logging/lineage and platform consistency, and supports transition of HPC users to the platform.

Lead design and delivery of FinOps products across Onyx cloud platforms: enable cost visibility, optimization, governance, reporting, and training by partnering with engineering, finance, and R&D stakeholders in an agile environment.