Jobs at GSK

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 pharmacovigilance and safety risk management for ViiV clinical assets. Interpret safety data, detect and escalate signals, advise on benefit-risk, support regulatory submissions, and represent safety in cross-functional governance. Lead Safety Review Teams, mentor colleagues, and drive safety strategy and process improvements across global clinical development.

Provide high-level administrative and operational support to the Onyx R&D team, managing complex diaries, travel and expenses, vendor and finance processes, onboarding, meetings and events, and general office administration across sites and time zones. Anticipate needs, protect leaders' time, and ensure smooth execution of logistical and operational tasks.

Lead product vision, roadmap and delivery for experimental data workflows across R&D. Partner with scientists, stakeholders and tech teams to prioritise backlog, drive agile delivery, ensure quality, compliance and data governance, and increase reuse and accessibility of experimental data. Promote adoption, work with vendors, and balance short-term delivery with long-term strategy to enable analytics and AI-enabled research.

Lead product strategy and delivery for Workday Payroll (UK, US, Canada). Own backlog, prioritise features, guide Associate Product Owners and delivery teams, ensure compliance, operational readiness, performance monitoring, and continuous improvement across the product lifecycle.

Lead UK market access strategy and tender activities for a vaccines portfolio. Manage cross-functional teams to secure routine immunisation access, forecast sales and profitability, localise global content, and support influenza pandemic preparedness while ensuring compliant, high-quality submissions and stakeholder engagement.

Design, develop, and optimize enterprise access network architectures (LAN/Wi‑Fi) across campuses, data centers and manufacturing. Provide technical leadership for network transformation, integrate access technologies with cloud, WAN, SASE and Zero Trust, define standards/policies, assess emerging tech (SD‑WAN, WiFi 8, campus fabric), oversee implementations, optimize performance and ensure disaster recovery readiness, and manage vendor relationships.

Lead European commercial strategy and launch readiness for GSK's lung oncology portfolio across EU4, UK and Area markets. Translate global strategy into local execution, drive launch sequencing, market access, performance management, cross‑functional alignment, and multiple product launches to maximise patient access and commercial outcomes.

Partner with R&D business leaders to deliver HR change initiatives, talent and leadership development, inclusion and engagement, data-driven people insights, and global HR project delivery within a complex matrixed organization.

The Document & Information Lead manages document control processes for major projects, ensuring compliance and data integrity while leading the document team and handling stakeholder communication.

Lead global business strategy, roadmap, and lifecycle for the Electronic Batch Record system in cGMP pharmaceutical manufacturing. Align stakeholders, define user requirements, oversee validation, testing, training, data integrity, deviations/CAPAs, and harmonization across sites. Support audits/inspections and partner with Tech and QA to deliver compliant releases and continuous improvement.

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.

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.

Develop scalable cloud infrastructure and robust software solutions for AI/ML, collaborating with engineers and scientists to enhance scientific research.

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.

Accountable for end-to-end product ownership across automation design and engineering. Translate business requirements into future-state, AI-enabled automation, drive delivery with engineering and vendors, oversee testing and launch, and align cross-workstream capabilities. Requires domain fluency in pharmaceutical R&D and executive stakeholder influence.

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