Future Tech Jobs
Future Tech Jobs
This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating them into clinical plans to optimize decision-making and patient stratification.
This role involves developing and implementing biomarker strategies to support the clinical development of late-stage oncology assets. Responsibilities include collaborating with cross-functional teams, validating biomarker strategies, and integrating them into clinical plans to optimize decision-making and patient stratification.
In this role, you will manage and improve stability data for small molecule studies, create and maintain study protocols, collect and analyse datasets, and produce clear summaries and visualisations for regulatory submissions. You will also support audits, collaborate with cross-functional teams, and drive process improvements through digital tool adoption.
This role involves providing hands-on engineering support within a sterile pharmaceutical manufacturing environment, focusing on maintenance, compliance, and continuous improvement of production systems. The technician will work across complex equipment and processes, ensuring GMP standards, managing SAP systems, and supporting projects such as new product introductions. Key responsibilities include breakdown repairs, PPM activities, calibration, and supervision of contractors in a regulated, shift-based operation.
This role involves providing real-time technical support for manufacturing operations, troubleshooting process issues, and driving continuous improvements in a regulated pharmaceutical environment. The technologist will work hands-on on the shop floor to ensure production efficiency, compliance, and product quality, while collaborating with cross-functional teams including engineering, quality, and production. Emphasis is placed on data-driven problem solving, maintaining audit readiness, and coaching frontline staff in GMP and technical standards.
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.
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.
This role involves leading the investigation and resolution of manufacturing deviations in a GMP-regulated environment, ensuring compliance and product quality. The Deviation Owner will coordinate root cause analyses, drive corrective actions, and work across quality, production, and engineering teams to prevent recurrence. Emphasis is placed on data-driven problem solving, governance of deviation processes, and continuous improvement through structured methodologies like DMA/IC.
This role involves leading the integration of new equipment, processes, and technologies into sterile manufacturing operations, ensuring compliance, safety, and minimal disruption to supply. The technologist will work across project lifecycles—from design and validation to handover—providing technical leadership and operational readiness support. Collaboration with engineering, quality, and digital manufacturing teams is key to deploying capital projects and new product introductions in a GMP-regulated environment.
Lead technical operations at a UK pharmaceutical manufacturing site, ensuring safe, compliant, and efficient production of medicines. Provide technical leadership, resolve process and equipment issues, and drive continuous improvement in a GMP-regulated environment. Collaborate with engineering, quality, and supply chain teams to maintain operational excellence and support audit readiness.
This role involves managing technology transfer projects for external contract manufacturing organizations (CMOs) in the pharmaceutical sector, ensuring alignment between GSK and suppliers on timelines, quality, and technical deliverables. The specialist will coordinate cross-functionally across procurement, quality, technical, and supply teams to operationalize new assets or suppliers, with a focus on sterile drug products like monoclonal antibodies and vaccines. Key responsibilities include maintaining critical path schedules, mitigating risks, and driving project governance from transfer through to product launch.
This role involves providing expert process safety leadership at GSK’s Barnard Castle manufacturing site, ensuring compliance with EHS regulations and delivering process safety improvements. The engineer will lead hazard assessments, support incident investigations, and drive safe working practices across production operations, with a strong focus on regulatory standards like DSEAR and CDM. The position plays a key part in maintaining safety integrity within a high-value, regulated pharmaceutical environment.
This role involves managing technology transfer projects for external contract manufacturing organizations in the pharmaceutical sector, ensuring alignment between GSK and suppliers. The specialist will oversee project schedules, mitigate risks, and ensure timely delivery of drug products across critical assets like monoclonal antibodies, vaccines, and small molecules. Collaboration with cross-functional teams and supplier relationship management are central to driving successful operationalization within budget and timeline.
This role involves managing technology transfer projects for external drug product manufacturing with Contract Manufacturing Organisations (CMOs). The specialist will coordinate cross-functionally across Procurement, Quality, Technical, and Supply teams to establish and maintain project schedules, mitigate risks, and ensure timely delivery of assets within budget. The position emphasizes strong stakeholder engagement, governance, and retention of manufacturing knowledge across the supply network.
The role involves working as part of a team to support automated inspection equipment and processes, including troubleshooting issues, managing technical projects, and providing technical data. You will act as a subject matter expert in automated leak detection and visual inspection technologies, collaborating with engineers and suppliers to ensure compliance with GMP and EHS standards.
