Latest Vaccines Jobs

Postdoctoral Research Scientist – Veterinary Vaccines Research

APHA scientific activity focuses on protecting UK against the threat of a wide variety of animal diseases. Research undertaken at APHA provides the scientific evidence that allows the Agency to provide expert advice and supports policy development for the Government.As...

Animal & Plant Health Agency Addlestone, New Haw, South East England, United Kingdom £47 – £52 pa

Permanent

Senior Director, Global Real-World Evidence & Health Outcomes Research Lead, RSV Vaccines

This role involves leading the generation and dissemination of real-world evidence and health outcomes research for GSK's RSV vaccines. Responsibilities include managing data generation plans, collaborating with cross-functional teams, and engaging with external stakeholders to ensure robust evidence supports product positioning and market access.

GSK United Kingdom

Senior Director, Global Real-World Evidence & Health Outcomes Research Lead, RSV Vaccines

This role involves leading the generation and dissemination of real-world evidence and health outcomes research for RSV vaccines. Responsibilities include managing data generation plans, collaborating with cross-functional teams, and engaging with external stakeholders to ensure robust evidence supports vaccine development and commercial success.

GSK

(Fixed Term) Manufacturing Associate I

Operate and maintain mRNA vaccine production equipment in compliance with cGMP and safety standards, executing manufacturing processes, troubleshooting equipment and digital systems, and supporting quality documentation and continuous improvement initiatives. Work within a cross-functional team to ensure timely batch release and operational excellence in a fast-paced, highly regulated environment.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Manufacturing Associate I

Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.

Moderna

On-site Temporary

Process / Equipment Engineer

The Process/Equipment Engineer provides technical support for the Bio-Vaccines Suites, ensuring equipment reliability and resolving manufacturing issues. Responsibilities include troubleshooting, leading investigations, validation, compliance, and continuous improvement initiatives.

Appcast Enterprise Dublin, Alba / Scotland, IV17 0YF, United Kingdom

Postdoctoral Research Assistant in Immunology

This role involves conducting advanced research in spatial immunometabolism, specifically focusing on the germinal centre reaction. The successful candidate will work within the Clarke group at the Kennedy Institute, developing new scientific techniques, guiding junior researchers, and contributing to research proposals and funding applications.

University of Oxford Oxford, South East England, United Kingdom £39 – £46 pa

On-site Contract

Undergraduate Clinical Development Scientist

Pfizer UK Undergraduate Programme 2027/2028Clinical Development Scientist UndergraduateVaccine Clinical ResearchWho can apply?Applicantsmust be completing a placement as part of a degree course at a UK University, either through Year in Industry/Industrial Placement or Gap Year.Please note that we will only...

Pfizer Marlow, United Kingdom

Postdoctoral Research Associate (Computational Vaccine Discovery)

This role involves developing a computational platform for malaria vaccine discovery, focusing on T-cell antigen and peptide prioritisation. You will work with large datasets, develop scalable workflows, and collaborate internationally to create reusable research outputs and scientific publications.

Liverpool School of Tropical Medicine Liverpool, Northern England, United Kingdom

Contract

Undergraduate Regulatory Strategist

This role involves working in Pfizer's Regulatory Strategy department, contributing to the development and implementation of regulatory strategies for innovative medicinal products. Responsibilities include compiling regulatory documents, engaging with health authorities, and maintaining systems and processes. The position offers a unique overview of the pharmaceutical product life cycle from research to market.

Pfizer United Kingdom

Research Assistant in Cancer Vaccine Epitope Discovery & Future mRNA Manufacturing

We are seeking to appoint a Research Assistant (AI Scientist & Computational Cancer Biology) to join the Nuffield Department of Medicine, University of Oxford, working on an state of the art project funded by Advanced Research & Innovation Agency.Reporting to...

University of Oxford Oxford, South East England, United Kingdom £35 – £41 pa

Contract

Process Technician 11-Month

Operate and monitor manufacturing processes in a cGMP-regulated biopharmaceutical environment, supporting the production of life-changing medicines. Perform troubleshooting, contribute to process improvements using Lean methodologies, and assist in validation and documentation activities. Work within a rotating shift pattern in a safety-focused, highly regulated team setting.

Appcast Enterprise Dublin, Alba / Scotland, IV17 0YF, United Kingdom

Contract

Head of Operational Excellence

The Head of Operational Excellence leads process improvement activities and staff, aligning projects with business strategies. They establish and maintain performance metrics, manage operational processes, and oversee training and development of subject matter experts in a regulated, global matrix organization.

CSL United Kingdom

Senior Scientist R&D

The Senior R&D Scientist will execute complex experimental workstreams, analyse data, and present findings to stakeholders. They will apply Design for Manufacture (DFM) principles to optimise product formulations and ensure compliance with GLP, GMP, and GDP standards in a laboratory setting.

Talentmark Stirling, Stirling And Falkirk, United Kingdom £25 – £27 ph

On-site Contract Clearance Required

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role focuses on end-to-end quality oversight of external vendors and suppliers involved in regulated R&D activities, ensuring compliance with GLP, GCP, GMP, and GVP standards. The individual will lead vendor qualification, audit management, quality agreement negotiation, and continuous performance monitoring, while collaborating with cross-functional teams including Clinical, CMC, Safety, and Legal. A key aspect is driving compliance, data integrity (ALCOA+), and continuous improvement across third-party partners through risk-based assessments, CAPA follow-up, and QMS integration.

CSL United Kingdom

On-site Permanent