Latest Innovation Jobs

Senior Director Translational Data Sciences

This role involves developing and executing a translational data strategy that bridges the gap between disease biology and clinical outcomes. The Senior Director will lead a team in integrating multi-omics data with AI-driven analytics, collaborate with R&D and clinical development, and establish high-value partnerships with external organizations.

GSK

On-site Permanent

Statistics Director, Oncology

This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and providing technical leadership to statisticians and statistical programmers. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to drive the development of new cancer therapies.

GSK United Kingdom

On-site Permanent

Engineering Technician (numerous vacancies)

Engineering Technicians at GSK's Ware site support production activities and site operations by performing maintenance, calibration, and repair tasks on manufacturing and utility equipment. They work in a team to ensure safety, quality, and reliability, and may be involved in project work and continuous improvement initiatives.

GSK East Hertfordshire, United Kingdom

On-site Permanent Shift-work

Senior Scientist ETCT

The Senior Scientist will work within the ETCT Biology Unit, contributing to pre-clinical and early clinical biologics programs. Responsibilities include designing and executing experiments, providing input on pharmacokinetics and non-clinical safety, and mentoring junior scientists.

GSK Stevenage, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities. You will evaluate compliance with GMP, policies, and regulatory requirements, and provide subject matter expertise on sterile manufacturing. The role requires strong communication and influencing skills, and involves travel to various sites across the network.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.

GSK Worthing, United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of risks and corrective actions.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Principal Scientist

This role involves leveraging cutting-edge computational approaches to understand and treat cancer. You will analyze and integrate multi-omics and clinical data to characterize disease heterogeneity, model disease evolution, and investigate treatment response. Collaboration with experimental and clinical teams is key to translating complex data into actionable insights for drug discovery.

GSK Stevenage, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects from internal and external donor sites to external Contract Manufacturing Organizations (CMOs). Key responsibilities include managing project schedules, mitigating risks, and ensuring timely delivery within budget, while acting as the main point of contact between GSK and suppliers.

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Worthing, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.

GSK Stevenage, United Kingdom

Hybrid Permanent

Operational Quality Director

The Operational Quality Director at GSK will lead the end-to-end quality oversight of manufacturing activities, ensuring compliance with GMP standards and regulatory requirements. Key responsibilities include managing batch documentation, overseeing real-time quality control, and leading the QP team to maintain high-quality standards and inspection readiness.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, collaborating with internal and external stakeholders to design and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key experts in the field.

GSK

Hybrid Permanent