Latest Technology Jobs

Deviation Owner

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.

GSK Barnard Castle, United Kingdom

On-site Permanent

Site Shift Manager

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.

GSK Barnard Castle, United Kingdom

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include evaluating quality strategies, driving continuous improvements, and supporting health authority inspections. The role also focuses on talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management. The role requires a deep understanding of regulatory requirements and the ability to lead a global quality team.

GSK

On-site Permanent

SERM Scientific Director

The SERM Scientific Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. This role involves driving pharmacovigilance activities, evaluating safety data, and collaborating with cross-functional teams to ensure robust benefit-risk profiles and patient safety. The position requires significant experience in pharmacovigilance and a strong understanding of global regulations.

GSK

On-site Permanent

Study Manager

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

GSK Stevenage, United Kingdom

Hybrid Permanent

Senior Director, Portfolio Integration Lead

This role leads scientific and strategic integration across GSK's oncology portfolio, ensuring alignment and innovation in clinical development for high-impact cancer therapies. The Senior Director acts as a cross-asset expert, shaping disease-level strategies, advancing biomarker and combination approaches, and driving clinical trial innovation. They work across matrix teams and governance bodies to align portfolio decisions with patient needs and scientific feasibility.

GSK Stevenage, United Kingdom

Hybrid Permanent

Analytical Chemistry - Platform Modalities Leader

This role involves leading the strategic expansion and modernization of analytical chemistry platforms for complex therapeutic modalities, including small molecules, drug conjugates, and oligonucleotides. The Platform Modalities Leader will drive the adoption of new technologies, ensure robust and scalable analytical capabilities, and provide hands-on technical leadership while influencing cross-functional teams.

GSK Stevenage, United Kingdom

On-site Permanent

Head of RII or Oncology Programming

This senior leadership role involves overseeing the transformation of clinical data into regulatory-ready evidence for GSK's Respiratory, Immunology & Inflammation (RII) or Oncology Research Unit. The Head of RII or Oncology Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality, compliance, and timely delivery of medicines and vaccines.

GSK Stevenage, United Kingdom

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global R&D trials, translating protocols into operational supply strategies, and ensuring on-time delivery of investigational products. The Clinical Trial Supply Manager acts as the key link between clinical teams and supply operations, overseeing demand planning, depot management, and compliance across Phase I–IV studies, including investigator-sponsored and compassionate use trials.

GSK Stevenage, United Kingdom €48,375 – €116,000 pa

On-site Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory submissions. The position requires strong technical expertise, collaboration across functions, and a focus on quality and compliance.

GSK East Hertfordshire, United Kingdom

On-site Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory compliance. The position requires strong technical expertise, collaboration across functions, and a focus on quality and patient safety.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

AI Strategy Director, Development Operations

The AI Strategy Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions that accelerate clinical trials and improve patient outcomes. Responsibilities include prioritizing AI opportunities, evaluating external capabilities, and leading cross-functional teams to prototype and deploy AI-enabled workflows.

GSK Stevenage, United Kingdom

On-site Permanent

CMC Leader (Director)

Leads end-to-end CMC strategy and execution for a pharmaceutical product from early development through commercialisation, including process development, regulatory filings, and lifecycle planning. Coordinates cross-functional global teams across R&D, supply chain, and regulatory to deliver clinical and commercial supply, ensuring technical transfer, quality compliance, and launch readiness. Focuses on complex modalities such as small molecules and oligonucleotides, with strong emphasis on regulatory strategy, risk management, and transition to commercial operations.

GSK Stevenage, United Kingdom

Hybrid Permanent

CMC Leader (Director)

Leads the development, industrialization, and lifecycle delivery of a physical medicine from early development through commercialization, ensuring seamless transition across stages. Coordinates cross-functional CMC and supply chain teams to deliver regulatory filings, process validation, and launch readiness, with a focus on complex products including small molecules and oligonucleotides. Drives strategic decision-making across R&D, manufacturing, and commercial functions to ensure timely, compliant, and scalable product supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent