Latest Vaccines Jobs

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance safety sciences functions, ensuring compliance with global regulatory standards and overseeing signal detection, safety data analysis, and process optimization. Provides strategic direction for evolving PV legislation and acts as a subject matter expert in audits and inspections. Supports drug development and post-marketing safety reporting while driving data visualization and analytical improvements.

CSL

Hybrid Permanent

Vaccines Safety Sciences Lead

Leads vaccine safety sciences functions, ensuring compliance with pharmacovigilance regulations and global safety standards. Oversees signal detection, safety data analysis, and regulatory documentation while guiding process improvements and cross-functional initiatives. Manages teams and supports regulatory inspections, safety reporting, and the implementation of data visualization tools for enhanced decision-making.

CSL

Hybrid Permanent

Medical Director, Oncology Clinical Development

This role involves leading oncology clinical trials from protocol design to study reporting, ensuring scientific integrity and alignment with regulatory and commercial goals. The Medical Director will collaborate with global experts and internal teams to advance GSK’s oncology pipeline, with a focus on data generation, safety monitoring, and strategic medical input across the clinical development lifecycle.

GSK Stevenage, United Kingdom US$222,750 – US$371,250 pa

Hybrid Permanent

Medical Director, Oncology Clinical Development

This role involves leading clinical research activities for GSK’s oncology portfolio, including designing and executing phase 1-3 trials, ensuring scientific integrity, and supporting regulatory submissions. The Medical Director will collaborate with internal and external experts to advance clinical development strategies and drive data generation in oncology. The position requires strong medical and scientific leadership in a matrix environment with a focus on patient impact.

GSK

Hybrid Permanent

Manager, Oncology Regulatory Strategy

This role involves leading and implementing regional regulatory strategies for oncology products in the Rest of World (ROW) region, ensuring alignment with global objectives and commercial goals. The individual will represent the region on the Global Regulatory Strategic Team, manage submissions and approvals, and shape interactions with health authorities. A key focus is ensuring compliance while influencing the regulatory environment to accelerate patient access to medicines.

Pfizer Marlow, United Kingdom

Manager, Oncology Regulatory Strategy

Leads regional regulatory strategy for oncology products across the Rest of World (ROW), ensuring alignment with global objectives and timely submissions to health authorities. Works closely with cross-functional teams and external agencies to shape regulatory pathways, influence policy, and secure commercially viable labeling. Focuses on compliance, risk mitigation, and strategic engagement in a dynamic regulatory environment.

Pfizer Sandwich, United Kingdom

(Fixed-Term) Manufacturing Associate I

Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.

Moderna Oxford, United Kingdom

(Fixed-Term) Manufacturing Associate I

This role involves operating and maintaining equipment in a cGMP-regulated mRNA vaccine production environment, ensuring safe and compliant manufacturing processes. The associate will execute production operations, support quality assurance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Work is conducted in a highly automated, digitally enabled facility with a focus on operational excellence and innovation in mRNA technology.

Moderna

Senior Scientist R&D

This role involves leading complex experimental workstreams in medical device R&D, from concept to design transfer, with a focus on diagnostic immunoassay technologies. The scientist will analyse multi-factorial data, optimise formulations using Design for Manufacture principles, and ensure compliance with GLP, GMP, and GDP standards in a laboratory setting. The position is based in Motherwell and supports critical development within a leading biopharmaceutical organisation.

Talentmark Calderbank, Lanarkshire, ML6 9TB, United Kingdom £20 – £23 ph

Junior Technical Specialist (Microbiology & Immunology)

Performs and oversees microbiology and immunology assays including bacterial culture, flow cytometry, ELISA, and functional immune testing to support vaccine research. Ensures high-quality, compliant laboratory operations within a regulated environment. Contributes to assay optimisation and troubleshooting in collaboration with senior scientists.

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

Contract

Senior Bioinformatics Scientist

A Senior Bioinformatics Scientist will define data requirements for AI models, design biologically sound datasets and evaluations, and ensure data integrity in training foundational genomic models. The role involves close collaboration with deep learning and engineering teams to validate model performance and biological relevance. Work focuses on sequence analysis, annotation, and evolutionary-scale data interpretation to support therapeutic discovery.

Basecamp Research London, United Kingdom

On-site Permanent

Associate Director, Device Lead

Lead technical strategy and lifecycle management for drug delivery devices across GSK’s global manufacturing network, ensuring regulatory compliance, supply robustness, and innovation in device design and manufacturing processes. Serve as the primary technical liaison between device suppliers and internal MSAT teams, driving technology transfer, risk management, and continuous improvement initiatives. Focus on quality by design, digital data management, and sustainable manufacturing within a regulated GMP environment.

GSK £142,725 – £237,875 pa

Associate Director, Device Lead

This role leads the global technical ownership of drug delivery device platforms, ensuring robust supply, regulatory compliance, and lifecycle management across GSK's manufacturing network. The individual will act as the primary technical interface with device suppliers, drive innovation in device technologies, and support technology transfer from R&D to commercialization. Key responsibilities include risk management, process optimization, and ensuring adherence to global medical device regulations and quality standards.

GSK £142,725 – £237,875 pa