Jobs at GSK

Lead statistical activities in oncology studies, employing innovative statistical methods to guide development decisions and ensure regulatory compliance.

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.

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.

The Supply Chain Support Specialist manages compliance and integrity of processes in the clinical supply chain, focusing on temperature excursions and collaboration across departments to ensure clinical supply continuity.

The role manages UK employment tax compliance, coordinating filings and governance while advising stakeholders on tax matters and process improvements.

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 Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and lifecycle stages. Collaborate with cross-functional teams, provide regulatory advice, and mentor colleagues while ensuring compliance and quality.

Drive global transformation in incoming material testing and data management by leading a matrix programme team, standardizing operations and improving QC processes.

The Commercial Head for Lung Europe will define and lead the European sales strategy for the lung oncology portfolio, manage product launches, drive performance, and ensure patient access to medicines across Europe.

The Specialist will manage extractables and leachables assessments, ensuring compliance, conducting risk assessments, and providing technical support for drug manufacturing processes.

Lead statistical planning and analysis for oncology clinical programs, mentor colleagues, and drive innovation within cross-functional teams.

The SERM Scientific Director leads pharmacovigilance, evaluates safety data, manages risks, supports regulatory submissions, and mentors in a cross-functional environment.

The role involves developing regulatory strategies in collaboration with global teams, ensuring compliance with regulations, and improving processes in oncology drug development.

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

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

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.