Latest Technology Jobs

Director, CMC Regulatory Affairs

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.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Steriles Operator - Multiple Positions Available

This role involves operating and monitoring semi-automatic and fully automatic packaging, assembly, and inspection equipment in a sterile manufacturing environment. You'll ensure product quality through visual inspections, maintain accurate batch documentation in compliance with GMP standards, and support the production of medicines and vaccines in a regulated, classified environment. The position requires working closely with cross-functional teams to resolve discrepancies and maintain efficient, compliant operations.

GSK Barnard Castle, United Kingdom

On-site Permanent

Head of RII or Oncology Programming

This role involves leading the clinical data programming for GSK's Respiratory, Immunology & Inflammation or Oncology Research Unit. Responsibilities include setting high standards for data quality, driving innovation with technologies like Generative AI, and collaborating with cross-functional teams to accelerate the development and submission of new medicines and vaccines.

GSK United Kingdom

On-site Permanent

Head of RII or Oncology Programming

This role involves leading the clinical data programming for GSK's Respiratory, Immunology & Inflammation or Oncology Research Unit. Responsibilities include setting high standards for data quality, driving innovation with technologies like Generative AI, and collaborating with cross-functional teams to accelerate the development and submission of medicines and vaccines.

GSK

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, or Oncology Research Units. The Head of Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality and compliance.

GSK

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK’s global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager will coordinate across depots, logistics partners, and clinical teams to maintain supply continuity, minimise waste, and support study milestones across phases I–IV. It requires strong planning, risk management, and GxP compliance in a patient-focused, global trial environment.

GSK Belgium €69,600 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the clinical trial supply chain for GSK's global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager coordinates across depots, logistics partners, and internal teams to maintain compliance, minimise waste, and support study milestones across all phases of clinical development.

GSK €48,375 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, translating protocols into supply strategies, and ensuring timely delivery of investigational products. The manager will lead supply planning, coordinate with depots and logistics partners, and act as the primary link between clinical teams and supply operations across Phase I–IV studies. Emphasis is placed on risk-adjusted, patient-focused planning and continuous improvement in compliance with GxP and regulatory standards.

GSK £48,375 – £116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, from protocol review to study close-out. The Clinical Trial Supply Manager ensures timely, compliant delivery of investigational products by translating protocols into supply strategies, managing inventory and distribution, and acting as the key link between clinical teams and supply operations across Phase I–IV studies.

GSK €48,375 – €80,625 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for global trials from protocol review to study close-out, ensuring timely delivery of investigational products while minimizing waste. The Clinical Trial Supply Manager acts as the key link between supply chain and clinical teams, developing risk-adjusted supply strategies, overseeing depot operations, and ensuring compliance with GxP and regulatory standards across Phase I–IV studies.

GSK €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 technology transfers, process verification, and product qualifications, while collaborating with R&D, manufacturing sites, and regulatory teams to ensure safe and compliant supply.

GSK Worthing, United Kingdom

Hybrid 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 technology transfers, process verification, regulatory submissions, and cross-functional investigations to ensure safe and compliant supply. The role emphasizes practical problem-solving and collaboration across functions.

GSK

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 with R&D and manufacturing sites, and a focus on robust and compliant supply.

GSK

On-site 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 to improve clinical trial outcomes. Responsibilities include prioritizing AI opportunities, evaluating vendor capabilities, and leading cross-functional teams to prototype and deploy AI-enabled workflows.

GSK United Kingdom

On-site 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 to accelerate clinical trials and improve patient outcomes. Key responsibilities include prioritizing AI opportunities, evaluating external vendors, and shaping deployment strategies with cross-functional teams.

GSK

On-site Permanent