Latest Technology Jobs

Steriles Business Change Lead

Lead business change initiatives for sterile manufacturing at a GSK site in Barnard Castle, ensuring operational readiness across quality, compliance, and production systems. Coordinate cross-functional teams through commissioning, validation, and go-live phases, with a focus on safety, regulatory compliance, and sustainable performance improvement in a highly regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Steriles Standards Manager

Leads the development and enforcement of operational standards for sterile manufacturing, ensuring compliance with regulatory requirements and driving continuous improvement. Works cross-functionally with quality, engineering, and operations teams to standardize processes, support audit readiness, and strengthen control in aseptic environments. Focuses on reducing variability, improving compliance, and coaching teams in a highly regulated pharmaceutical setting.

GSK Barnard Castle, United Kingdom

On-site Permanent

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways, ensuring biomarker datasets are reusable and accessible. Key responsibilities include resolving systemic barriers, aligning data delivery with decision timelines, and developing repeatable processes for data re-use across multiple functions.

GSK Stevenage, United Kingdom

Hybrid Permanent

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

Leads drug product development for sterile long-acting injectables and oligonucleotides, guiding cross-functional teams in formulation, process development, and technology transfer. Ensures robust CMC strategies, regulatory compliance, and supply readiness across clinical to commercial phases. Focuses on delivering high-quality, patient-centric medicines through scientific leadership and matrix collaboration.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

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

Leads late-stage drug product development for sterile long-acting injectables and oligonucleotides, guiding cross-functional teams in formulation, process development, and technology transfer. Translates CMC and regulatory strategies into actionable plans, ensuring robust control strategies and compliance across clinical and commercial phases. Works within a matrix environment to align R&D, manufacturing, and supply chain functions for successful asset delivery.

GSK Stevenage, United Kingdom

Hybrid Permanent

VP and Head of Operational Effectiveness

Leads operational effectiveness for clinical trial programs across GSK’s R&D organisation, driving process reimagination, performance intelligence, and transformation to accelerate drug development. Focuses on data-driven insights, operational excellence in third-party delivery and documentation, and capability building to improve speed, quality, and compliance in clinical operations.

GSK Stevenage, United Kingdom €190,500 – €317,500 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating submissions and ensuring compliance with global regulations. Works across cross-functional teams to address complex regulatory challenges and support continuous supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a matrix environment.

GSK Stevenage, United Kingdom €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for pharmaceutical 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 projects.

GSK London, United Kingdom £90,000 – £150,000 pa

Hybrid Permanent

Executive Medical Director, Clinical Development Lead - Oncology

This role leads the clinical strategy and scientific vision for oncology assets across their lifecycle, shaping high-impact drug development from discovery to real-world application. The Executive Medical Director acts as a strategic leader within cross-functional teams, driving data-driven decision-making, regulatory engagement, and innovation through AI and advanced analytics. They are responsible for integrating clinical, regulatory, and commercial considerations to advance treatments for cancers with high unmet need.

GSK Stevenage, United Kingdom US$242,250 – US$403,750 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development to commercial manufacturing. The Molecule Steward ensures robust product control strategies, drives continuous process improvement, and coordinates technical strategy across drug substance, drug product, and analytical teams. The position requires deep scientific expertise, regulatory knowledge, and leadership in a matrixed global environment to maintain product quality and manufacturability.

GSK East Hertfordshire, United Kingdom €103,500 – €172,500 pa

Hybrid Permanent

Director, Clinical Science Oncology Clinical Development

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune...

GSK Exeter, EX4 4HD, United Kingdom

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent