Jobs at GSK

Performs microbiological testing, sample collection, environmental and process monitoring within a GMP pharmaceutical manufacturing environment. Verifies results, supports batch approval and product release, conducts investigations and root-cause analysis, manages laboratory improvement initiatives, maintains equipment standards, and trains microbiology staff. The role provides expert analytical support while ensuring data integrity, regulatory compliance, safety, and consistent application of aseptic and microbiological techniques.

Integrate oncology clinical expertise with artificial intelligence and machine learning research in drug discovery and development. Identify and scope clinical AIML use cases, guide large language model applications, interpret multimodal clinical and biological data, validate algorithmic outputs, and support target and biomarker discovery. The role also partners with clinical development and translational research teams while maintaining weekly research clinic engagement.

Leads GSK’s enterprise Organisational Culture Assurance capability, developing assurance strategy, culture-risk frameworks, methodologies and annual plans. Oversees targeted reviews, behavioural analytics, AI-enabled insights and executive dashboards to identify cultural and behavioural risks. Integrates culture considerations into internal audit, advises senior leaders and Board committees, and leads a multidisciplinary specialist team. Requires significant experience in audit, risk, compliance, HR or organisational development, with strong analytical, influencing and leadership capabilities.

Leads organisational culture risk assessments and assurance reviews using quantitative and qualitative analysis. The role identifies behavioural patterns, leadership and accountability risks, and cultural factors affecting governance, risk management and performance. Responsibilities include developing dashboards, analysing people and operational data, advising audit teams, engaging senior stakeholders, facilitating discussions, and supporting enterprise-wide culture reporting and AI-enabled analytical methods.

Conduct trace analysis of extractables and leachables, mutagenic and elemental impurities using LC-MS, GC-MS and ICP-MS/OES. Develop, optimize, validate and verify analytical methods; create sample preparation approaches; interpret data; produce reports; assess risks; support regulatory submissions; and oversee CRO work packages in a pharmaceutical development environment.

Leads global procurement strategy for a technology professional services portfolio valued up to £350 million. Develops sourcing, contracting, supplier, and category strategies; leads complex negotiations; manages strategic technology partners; drives cost savings, resilience, innovation, compliance, and measurable benefits. Partners with senior Technology, Finance, Procurement, and business stakeholders while developing procurement teams and communicating strategies across global networks.

Participate in a two-year pharmaceutical quality science graduate programme involving laboratory testing, manufacturing quality control, regulatory compliance, quality systems, risk management, sustainability, and continuous improvement. Gain experience with analytical techniques, microbiology, chromatography, deviations, CAPA, change control, documentation, and cross-functional collaboration across manufacturing, R&D, technical services, and supply chain. Apply data analytics, Lean Six Sigma, and structured problem-solving to improve pharmaceutical and vaccine production processes.

Two-year engineering graduate programme focused on pharmaceutical manufacturing. Responsibilities include designing and commissioning equipment, improving reliability and automation, applying AI and data analytics, managing engineering projects, supporting predictive maintenance, optimizing control systems and robotics, and contributing to sustainability and continuous-improvement initiatives.

Industrial placement roles in biostatistics, clinical programming, and quantitative sciences innovation. Responsibilities include clinical trial design, statistical analysis, dataset and reporting development, quality control, machine learning, prediction modeling, and cross-functional collaboration supporting drug and vaccine development. Placements involve R, SAS, Python, GitHub, statistical methods, regulatory standards, and agile project delivery.

Industrial placement supporting pharmaceutical microbiology, Quality Control testing, environmental monitoring, validation, laboratory investigations, and continuous improvement projects. Responsibilities include preparing and testing samples, maintaining laboratory equipment, interpreting microbiological data, writing technical reports, following quality standards, and supporting contamination-control and compliance activities within GSK laboratories.

One-year onsite pharmaceutical science industrial placement across GSK sites in Ware, Worthing, or Barnard Castle. Placements support pharmaceutical manufacturing, MSAT, GMP compliance, process validation, troubleshooting, deviation investigations, continuous improvement, product transfers, quality systems, data analysis, and technical reporting. Applicants must have completed at least two years of an undergraduate degree, remain enrolled at a UK or ROI university, and start in July 2027.

Lead global procurement and category management for Travel, Meetings and Expenses. Develop sourcing strategies, negotiate contracts, govern suppliers, deliver savings, improve compliance, and support digital transformation. Use analytics to optimize costs, service, traveler experience, wellbeing, and carbon reduction. Influence senior stakeholders and regional procurement teams across a global matrixed organization while ensuring regulatory, tax, duty-of-care, and supplier performance requirements are met.

Leads strategic procurement for outsourced large-molecule manufacturing, including category strategy, sourcing, complex contract negotiations, supplier relationship management, capacity agreements, and supply-continuity initiatives. Partners with Procurement, Manufacturing Operations, R&D, Technical, Supply Chain, Quality, Finance, Legal, and product teams to support product launches, technology transfers, supplier transitions, and resilient biologics drug substance and drug product supply.

Leads pharmacovigilance and safety evaluation activities for GSK products across clinical development and post-marketing settings. Responsibilities include signal detection, safety assessments, risk management plans, regulatory safety reports, safety governance, risk minimization, audit follow-up, and cross-functional communication. The role investigates safety issues, supports benefit-risk decisions, and communicates safety positions to internal and external stakeholders.

Lead statistical strategy and execution for oncology clinical development across phases. Design and analyze trials using simulation, Bayesian and real-world data approaches; author protocols/SAPs; deliver timely, high-quality statistical outputs; influence asset and regulatory strategy; represent biostatistics externally and mentor project teams.

Leads AI and technology adoption across pharmaceutical R&D programs. Develops change and adoption plans, assesses readiness and risks, coordinates stakeholders, supports implementation of AI tools and data platforms, tracks adoption and value measures, and delivers focused transformation projects. The role translates technology changes into process, role, behavior, and capability improvements while building sustainable internal capability and influencing senior technical and business stakeholders.

Leads enterprise AI and technology adoption across pharmaceutical R&D, connecting behavior and process change to measurable business value. Builds an internal adoption capability, establishes a hub-and-spoke operating model, develops adoption roadmaps and measurement frameworks, and partners with technology programs to improve delivery and sustained usage. The role influences senior scientific and technology leaders, coordinates cross-functional transformation initiatives, and balances strategic leadership with hands-on execution.

Leads strategic technology transformation across pharmaceutical R&D programs. Partners with senior scientific, technology, and business leaders to shape strategy, roadmaps, investment decisions, operating models, partnerships, and business cases. Evaluates program progress, risks, value delivery, and build-versus-buy choices while identifying reusable capabilities and removing barriers. Requires significant pharmaceutical R&D or biotechnology experience, strong drug research knowledge, strategic project leadership, structured analysis, and executive-level influencing skills.

Acts as a strategic HR partner to senior UK Commercial leaders, translating business and talent strategies into workforce, leadership, capability, culture, and transformation plans. Advises on organisational design, employee relations, consultation obligations, reward, succession, and UK employment law. Uses workforce analytics and organisational insight to identify risks and opportunities, supports large-scale change, and influences stakeholders across a complex, matrixed organisation.

Industrial placement opportunities across GSK engineering, pharmaceutical manufacturing, process development, automation, sustainability, facilities, maintenance, and R&D teams. Students will support equipment installation, reliability, process optimisation, data analysis, modelling, validation, continuous improvement, sustainability initiatives, and capital projects. Placements are approximately one year starting July 2027, with roles based in Ware, Montrose, Stevenage, Worthing, or Barnard Castle. Most roles require full-time onsite work, while some offer flexible arrangements.