Latest Vaccines Jobs

Senior Director, Head, Vaccines and Infectious Diseases, Global Epidemiology and RWE

This role involves providing strategic leadership in epidemiology, leading a global team of VID epidemiologists, and collaborating across R&D functions. Responsibilities include designing and executing epidemiological studies, contributing to regulatory submissions, and driving innovation in methodologies and tools.

GSK

Hybrid Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves providing hands-on IT support for Moderna’s GMP manufacturing operations at the Harwell site. Key responsibilities include ensuring GMP compliance, triaging IT incidents, managing infrastructure, and collaborating with various teams to maintain robust and compliant systems. The position offers exposure to modern observability and cybersecurity tools, making it a dynamic opportunity for someone who thrives in complex, regulated environments.

Moderna Oxford, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves supporting Moderna’s manufacturing operations at the Harwell site, ensuring GMP compliance and providing Tier 1 IT support. Responsibilities include maintaining robust IT systems, triaging incidents, managing infrastructure, and collaborating with various teams to ensure smooth operations. The position offers exposure to modern cybersecurity and automation tools, making it a dynamic and challenging opportunity in the biotech industry.

Moderna

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

The Senior Manager, HTA, Value & Evidence (HV&E) role involves developing and executing strategic efforts to support patient access and reimbursement for rare disease treatments. This includes managing health economics and outcomes research, generating real-world evidence, and collaborating with cross-functional teams to demonstrate the value of Pfizer's medicines.

Pfizer

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer will be responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer United Kingdom

On-site Permanent

GMP Vendor Oversight and QA Lead

This role involves leading the quality oversight of external partners in R&D and regulated activities, ensuring compliance with GxP standards. Responsibilities include vendor lifecycle management, risk-based monitoring, quality agreements, and cross-functional collaboration to maintain high-quality standards and continuous improvement.

CSL United Kingdom

On-site Permanent

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

VP, Medicine Development Leader - Respiratory

Leads global development of a respiratory medicine from clinical proof of concept to approval, aligning cross-functional teams across R&D, manufacturing, and commercial functions. Defines strategic vision, manages development plans, regulatory submissions, and lifecycle strategy while ensuring patient-focused innovation and compliance. Acts as primary point of accountability and spokesperson to senior leadership and external stakeholders.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

This role leads the global development of a respiratory medicine from proof of concept through to approval, serving as the primary accountable leader across a cross-functional matrix team. The VP will define strategic direction, oversee clinical and regulatory execution, and align development with GSK’s broader R&D and commercial strategy, while engaging with senior leadership and external stakeholders to advance patient-focused innovation.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

Leads global development of a respiratory medicine from clinical proof of concept through approval, serving as the primary accountable leader across a cross-functional matrix team. Defines strategic vision, drives evidence generation, lifecycle planning, and regulatory strategy while coordinating input from R&D, manufacturing, commercial, and regulatory stakeholders to deliver patient-focused therapies.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent

AI Acceleration Lead

This role focuses on driving AI innovation in clinical development by identifying operational bottlenecks, designing and running AI pilots, and translating findings into scalable solutions. The person will work across clinical operations, technology teams, and vendors to validate AI tools, generate evidence of value, and guide investment decisions. Emphasis is placed on hands-on testing, change management, and enterprise-wide adoption of AI-native capabilities.

GSK Stevenage, United Kingdom

On-site Permanent

AI Acceleration Lead

Lead the design and execution of AI pilots to solve operational challenges in clinical development, working across clinical operations, technology teams, and vendors. Drive evidence-based scaling of AI solutions, validate feasibility using AI-native tools, and translate findings into strategic recommendations for enterprise adoption.

GSK United States

On-site Permanent

AI Acceleration Lead

The role involves identifying and executing AI-driven pilot projects to solve operational challenges in clinical development, working closely with clinical teams, technology partners, and vendors. The focus is on validating AI solutions, measuring impact, and driving scalable adoption across GSK’s Development Operations. It emphasizes hands-on testing, evidence-based decision-making, and translating innovation into measurable improvements in trial delivery and patient outcomes.

GSK

On-site Permanent

AI Acceleration Lead

This role focuses on driving AI innovation within clinical operations at GSK, identifying high-impact use cases, designing and running AI pilots, and translating findings into scalable solutions. The position works across clinical teams, technology partners, and enterprise AI functions to validate AI tools, improve trial delivery, and deliver measurable operational value through hands-on prototyping and cross-functional collaboration.

GSK

On-site Permanent