Latest Vaccines Jobs

Labelling Strategy and Development, Oncology Team Lead

This role involves leading a global labelling team for oncology products, shaping clear and compliant product labels that support patient care and regulatory success. The position requires strategic oversight of labelling development from early stages through lifecycle management, working closely with cross-functional teams and regulatory authorities to drive innovative, patient-focused solutions.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labelling across the drug development lifecycle. This role shapes regulatory-compliant, patient-focused labels by collaborating with cross-functional stakeholders in R&D, Regulatory, Safety, and Commercial. It involves strategic decision-making, engagement with health authorities, and driving innovation in labelling standards to support GSK’s oncology portfolio.

GSK

Hybrid Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

Moderna

On-site Permanent

Computational Biologist

The role involves applying expertise in -omics and imaging, using state-of-the-art computational methods to support drug discovery and development, particularly in Hepatology. Responsibilities include generating and evaluating genomic and histopathology imaging evidence, collaborating with multi-disciplinary teams, and communicating results to peers and leaders.

GSK Stevenage, United Kingdom

Hybrid Permanent

Principal Scientist, Innovation ETCT

The Principal Scientist role involves leading target discovery and early biologics programs, specifically focusing on antibody drug conjugates (ADCs) and T cell engaging bispecific antibodies (TCEs). You will collaborate with internal and external teams to accelerate the development of next-generation biologics for cancer therapy, contributing to the preclinical development of novel biologics.

GSK Stevenage, United Kingdom

Hybrid Permanent

Engineering Technician

The Engineering Technician role involves providing comprehensive engineering support for the Steriles Business Unit, focusing on equipment maintenance, GMP compliance, and continuous improvement initiatives. Responsibilities include breakdown repairs, calibration, quality documentation, and project support, all while maintaining high safety and regulatory standards.

GSK Barnard Castle, United Kingdom

On-site Permanent Shift-work

Statistics Director, Oncology

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

GSK Stevenage, United Kingdom

On-site Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent

Laboratory Analyst

The Laboratory Analyst supports product testing and analysis within GMP-compliant laboratories at GSK’s Ware site, ensuring safe and effective oral and solid dose medicines are produced. The role involves sample preparation, analytical testing using methodologies like HPLC, and maintaining compliance with safety and quality standards. Collaboration with cross-functional teams is key to maintaining supply and driving continuous improvement in a fast-paced manufacturing environment.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

This role involves managing and improving stability data for small molecule studies, creating and maintaining study protocols, and producing clear data visualizations for regulatory submissions. You will work closely with cross-functional teams and external partners to drive process improvements and ensure data integrity.

GSK Stevenage, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

In this role, you will manage and improve stability data for small molecule studies, create and maintain study protocols, collect and analyse datasets, and produce clear summaries and visualisations for regulatory submissions. You will also support audits, collaborate with cross-functional teams, and drive process improvements through digital tool adoption.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Process Safety Engineer

This role involves providing expert process safety leadership at GSK’s Barnard Castle manufacturing site, ensuring compliance with EHS regulations and delivering process safety improvements. The engineer will lead hazard assessments, support incident investigations, and drive safe working practices across production operations, with a strong focus on regulatory standards like DSEAR and CDM. The position plays a key part in maintaining safety integrity within a high-value, regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK United Kingdom

Hybrid Permanent