Jobs at GSK

Lead product strategy and delivery for clinical trial site and operations-facing tools, driving AI-first solutions, GxP-compliant releases, stakeholder alignment, adoption, and financial oversight across feasibility, start-up, contracting, budgeting and monitoring workflows.

Lead global strategy-to-execution for the GIST brand in oncology: establish governance and operating cadence, integrate cross-functional plans, drive launch readiness and budget alignment, resolve cross-functional barriers, and improve ways of working across functions and markets.

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.

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

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 CMC for a medicine from pre-C2P2 through P3/commercial process, file and launch. Own strategy, development, tech transfer, PPQ/CPV readiness, regulatory filing and global launch readiness, manage multi-disciplinary teams and external CDMOs, oversee budgets and lifecycle post‑launch transition to supply chain leadership.

Lead development, authoring and maintenance of Global Datasheets and local prescribing/patient information across markets. Partner with clinical, safety and regulatory colleagues to ensure accurate labelling, author regulatory responses, manage labelling implementation, maintain documentation in systems (eg Veeva Vault), support governance, mentor colleagues and represent GSK externally as needed.

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 development, industrialisation, and lifecycle delivery of assigned physical medicines from Commit to Phase 2 through Phase 3/commercial process, regulatory filing, launch readiness and transfer to global supply. Drive cross-functional CMC, DS/DP, analytical, manufacturing, supply chain, quality and regulatory strategies, manage risks, deliver PPQ/CPV/PAI readiness, and ensure seamless knowledge transfer and lifecycle follow-on activities.

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

Provide regulatory and compliance oversight for API and finished product manufacture and NPI launches. Develop regulatory strategies, lead submissions and licence maintenance, support QMS/cGMP adherence, manage deviations and audits, liaise with central regulatory groups and LOCs, and ensure site licences and product specifications meet pharmacopoeial and market requirements.

Lead engineering performance at External Manufacturing sites, ensuring product delivery through site assessments, capital management, and troubleshooting. Focus on Large Molecule Drug Substance activities, enhancing operational excellence and project delivery.

Lead product strategy and execution for an enterprise molecule design portfolio, driving AI/GenAI, LLMs, and autonomous agents adoption; build and mentor product teams; define technical architecture, data governance, MCPs, and buy-vs-build decisions to accelerate drug discovery and modernize legacy tools.

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.