Latest Technology Jobs

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects from internal and external donor sites to external Contract Manufacturing Organizations (CMOs). Key responsibilities include managing project schedules, mitigating risks, and ensuring timely delivery within budget, while acting as the main point of contact between GSK and suppliers.

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Worthing, United Kingdom

Hybrid Permanent

SERM Scientific Director

The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.

GSK

On-site Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development through manufacturing and commercial supply. The Molecule Steward ensures product quality, process robustness, and regulatory compliance by leading technical strategy, coordinating cross-functional teams, and driving continuous improvement across global supply chain sites. The position requires deep scientific expertise, strong leadership in matrixed environments, and active involvement in regulatory submissions and lifecycle management.

GSK €103,500 – €172,500 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, robustness, and compliance by leading technical strategy, process optimization, and cross-functional collaboration across R&D, manufacturing, and regulatory teams. They play a key role in technology transfer, continuous process verification, and maintaining control strategies in a highly regulated environment.

GSK €103,500 – €172,500 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, regulatory compliance, and process robustness by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives. It requires deep scientific expertise, strong leadership in matrixed environments, and coordination across R&D, manufacturing, and regulatory functions.

GSK €103,500 – €172,500 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 product quality, robustness, and manufacturability by leading technical strategy, process optimization, and regulatory compliance across global supply chain teams. The position requires deep scientific expertise, cross-functional collaboration, and leadership in resolving complex technical challenges in a regulated environment.

GSK €103,500 – €172,500 pa

Hybrid Permanent

Privacy Lead – R&D / Chief Patient Office (CPO)

This role involves leading privacy strategy and compliance for R&D and patient-focused initiatives at GSK, ensuring responsible data use in clinical research, digital health, and AI-driven projects. The Privacy Lead embeds privacy-by-design principles, conducts risk assessments, and supports governance across highly regulated environments, balancing innovation with ethical data practices.

GSK

Hybrid Permanent

SERM Medical Director

The SERM Medical Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. Key responsibilities include interpreting safety data, managing safety signals, and providing expert medical input to support benefit-risk decisions. This role involves leading cross-functional teams, collaborating with regulatory authorities, and shaping the safety strategy for innovative oncology medicines.

GSK

On-site 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 United Kingdom

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

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

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

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

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