Latest Vaccines Jobs

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, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site 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

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

On-site Permanent

Senior Systems Engineer, GXP Systems

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, 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

Director, Translational Science Lead

This role leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, focusing on biomarker development and validation to support clinical decision-making from preclinical through to launch. The position drives innovation in human translation using advanced technologies and multi-omics data, while providing strategic input across drug development and business development opportunities.

GSK US$178,200 – US$297,000 pa

Hybrid Permanent

Director, Translational Science Lead

Leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, driving biomarker development and validation from preclinical to clinical stages. Integrates multi-omics, human tissue data, and novel technologies to inform drug development decisions and support clinical trial design. Works cross-functionally to align translational insights with research, clinical, and regulatory teams.

GSK US$178,200 – US$297,000 pa

Hybrid Permanent

AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include prioritizing AI opportunities, evaluating external capabilities, and leading the deployment of AI-enabled workflows across the organization.

GSK

On-site Permanent

AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include prioritizing AI opportunities, evaluating external capabilities, and leading the deployment of AI-enabled workflows across the organization.

GSK

On-site Permanent

AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions that create meaningful value in clinical trials. Responsibilities include prioritizing AI opportunities, evaluating vendor capabilities, and leading the deployment of AI-enabled workflows across the organization.

GSK

On-site Permanent

Programming Leader

The Programming Leader will oversee project-level and study-level programming strategy and delivery for multiple complex studies in GSK's global pipeline. You will collaborate with cross-functional teams, ensure high-quality outputs, and champion agile methodologies and new technologies to enhance programming efficiency and data analysis.

GSK

Hybrid Permanent

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways at GSK. Key responsibilities include ensuring biomarker datasets are reusable, accessible, and aligned with translational decision-making, while also identifying and resolving systemic barriers and developing repeatable processes.

GSK

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

This role leads the global development of a respiratory medicine from clinical proof of concept through to regulatory approval, serving as the primary accountable leader across a matrixed cross-functional team. The VP will define strategic direction, oversee clinical and regulatory planning, manage budgets, and ensure alignment with GSK’s broader R&D and commercial objectives. The position involves high-level stakeholder engagement, lifecycle planning, and external representation to regulators and advisory bodies.

GSK United States £309,750 – £516,250 pa

Hybrid Permanent

VP, Medicine Development Leader - Respiratory

Lead the global development of a respiratory medicine from clinical proof of concept through to first-market approval, serving as the single point of accountability. You will build and lead a cross-functional matrix team, define strategic direction, and ensure alignment with GSK’s R&D and commercial strategies. The role involves shaping lifecycle plans, making evidence-based go/no-go decisions, and engaging with regulators and senior leadership to deliver patient-focused medical solutions.

GSK US$309,750 – US$516,250 pa

Hybrid Permanent