Future Tech Jobs
Future Tech Jobs
This role involves leading the generation of strategic insights for a key oncology brand within GSK's ADC portfolio. Responsibilities include shaping commercial forecasts, conducting global market research, and partnering with cross-functional teams to drive business strategy and competitive intelligence.
As a Senior Engineering Technician, you will provide comprehensive engineering support for the Sterile Value Stream, ensuring all production processes meet business and regulatory requirements. You will lead and supervise the Engineering Technician team, manage equipment breakdowns, and drive continuous improvement initiatives in a shift-based environment.
This role involves leading the RTSM function, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.
The Process Engineer role involves providing technical expertise to support safe and efficient manufacturing at GSK's Montrose site. Responsibilities include resolving technical issues, contributing to capital projects, improving process plant software, and collaborating with cross-functional teams to ensure compliance and process improvements.
Leads global CMC regulatory strategy for small molecule medicines, shaping development and approval pathways across international markets. Works at the intersection of R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient access. Focuses on solving complex regulatory challenges, mentoring talent, and improving processes to support long-term product success.
As a Process Technologist, you will support the production area by providing technical services, troubleshooting, and working on technical projects. You will collaborate with cross-functional teams to ensure product quality and compliance, execute process validation, and perform root cause analysis for material and processing issues.
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 24/7 manufacturing operations outside core hours at GSK’s Barnard Castle site, ensuring safety, compliance, and supply chain continuity. The Site Shift Manager acts as the primary on-site leader during shifts, coordinating production, managing incidents, and aligning cross-functional teams including manufacturing, quality, and engineering. Emphasis is placed on real-time decision-making, audit readiness, and continuous improvement in a regulated pharmaceutical environment.
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.
This role leads operational excellence for Supported Studies at GSK, focusing on data governance, system ownership, and digital integration. The individual will ensure data integrity, drive compliance with regulatory requirements like Transfer of Value, and translate operational needs into scalable digital solutions. Working across cross-functional teams, they will enhance efficiency, quality, and transparency in clinical operations through robust dashboards, automation, and process improvements.
This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies, ensuring data integrity, system performance, and compliance. The individual will lead data governance, dashboard development, and system integration—particularly for platforms like Veeva and IdeaPoint—while acting as a bridge between business and technology teams to drive efficiency and compliance in clinical study delivery.
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.
