Biotechnology Jobs

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on shaping regulatory approaches and mentoring teams in a complex, science-driven environment.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Lead CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Work cross-functionally to ensure compliance, support inspections, and maintain product supply. Influence regulatory decisions and mentor teams within a complex, matrixed environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, ensuring compliance with global regulations and supporting submissions, inspections, and supply continuity. Works cross-functionally to shape regulatory approaches and mentor teams, with a focus on innovation and risk mitigation in complex regulatory environments.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex international environments.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and ensuring compliance with global regulations. Works cross-functionally to address complex CMC issues, support inspections, and influence regulatory decisions. Focuses on maintaining product supply and optimizing regulatory processes across international markets.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK United States US$144,375 – US$240,625 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

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

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

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

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

Director, DP Workstream Leader – Small Molecule Parenteral (LAIs and Oligos)

This role involves leading late-stage drug product development for sterile long-acting injectables and oligonucleotides, overseeing formulation, process development, and technology transfer across clinical and commercial phases. The position acts as a strategic bridge between CMC project teams and functional execution, ensuring regulatory robustness, supply readiness, and integrated solutions through cross-functional leadership. It emphasizes scientific excellence, risk mitigation, and patient-focused innovation within a hybrid working model.

GSK United States

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

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