Jobs in Reading

NPI Launch Lead

This role leads the logistics and project management for new pharmaceutical and consumer product launches at GSK’s Barnard Castle site, ensuring timely, compliant market rollouts. The NPI Launch Lead coordinates cross-functional teams, manages launch timelines across global markets, and ensures adherence to GMP, quality, and regulatory standards throughout the product introduction lifecycle.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Operational Technologist

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.

GSK Barnard Castle, United Kingdom

On-site Permanent

Associate Director, Global Regulatory Science, CMC

Lead global CMC regulatory strategy for mRNA medicines, guiding international submissions and ensuring compliance with health authority requirements. Collaborate with manufacturing and quality teams to support product development across vaccines, oncology, and rare diseases. Develop and maintain regulatory documentation in CTD format, while driving process improvements and change control assessments.

Moderna

Hybrid Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently and in compliance with regulatory standards. The specialist coordinates with CROs, vendors, and internal teams to maintain supply chain continuity, troubleshoot logistics, and support digital innovation in supply systems, including AI-enabled tools and IRT platforms.

Moderna

Hybrid Permanent

Global Labelling Manager, Content

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels and regulatory guidance, and ensuring compliance with global standards across the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis London, United Kingdom

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing processes to generate and apply high-quality medical insights across Pfizer. Key responsibilities include developing Medical Insights strategies, prioritizing use cases, translating complex data into actionable insights, and embedding these insights into core medical processes to support informed decision-making and strategic discussions.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on leveraging advanced analytics and AI to translate complex medical data into strategic decisions, ensuring consistency and value across Pfizer’s medical portfolio.

Pfizer

On-site Permanent

Senior Director, AI Commercial Business Partner - Biopharmaceuticals Business Unit Europe & Canada

This role involves leading AI commercial initiatives and translating business needs into AI use cases for the Biopharmaceuticals Business Unit in Europe and Canada. The Senior Director will work closely with business teams and technical experts to drive the adoption and lifecycle management of AI solutions, ensuring they deliver measurable business impact and enhance customer engagement.

AstraZeneca

Hybrid Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on safety evaluation in clinical development and post-marketing settings. The Scientific Director will lead cross-functional teams, drive safety governance, and ensure regulatory compliance across international markets. The position requires deep expertise in drug safety, signal detection, and benefit-risk assessment to protect patient safety and support regulatory submissions.

GSK United States US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation in clinical development and post-marketing settings. The Scientific Director provides expert scientific input into safety governance, drives cross-functional teams, and ensures compliance with global regulatory standards. They play a key role in signal detection, safety surveillance, and shaping long-term clinical strategies to protect patient safety.

GSK US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management for GSK's global assets, ensuring scientifically sound review and interpretation of safety data. The director will develop and execute safety strategies, manage safety governance, and lead cross-functional teams to address product safety issues and ensure patient safety globally.

GSK

On-site Permanent

SERM Scientific Director

The SERM Scientific Director role involves leading pharmacovigilance and risk management planning, developing safety strategies, and ensuring the scientific soundness of data reviews. The position requires expertise in evaluating safety risks, managing cross-functional teams, and communicating safety issues to senior management.

GSK

On-site Permanent

Associate Director, Operations Excellence Supported Studies

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.

GSK Stevenage, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

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.

GSK London, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent