Latest Operations Analyst - Internship Jobs

(Fixed-Term) Manufacturing Associate II - Shift Position

This role involves operating production equipment for mRNA vaccines in compliance with cGMP and safety regulations, performing routine maintenance, troubleshooting technical issues, and supporting continuous improvement initiatives within a 24/7 manufacturing environment. The candidate will work on the manufacturing floor at Moderna’s Harwell site, contributing to the production of safe and effective vaccines using cutting-edge mRNA technology. Emphasis is placed on digital proficiency, attention to detail, and active participation in a dynamic, cross-functional team.

Moderna

On-site

Senior Director, Targets and Mechanisms Solutions

Lead the strategic direction and AI-driven innovation of Pfizer’s Targets and Mechanisms platforms, delivering scalable, science-centric digital solutions to accelerate drug discovery. Oversee a global team integrating advanced data technologies, AI, and predictive analytics across research units including Oncology, Vaccines, and Inflammation & Immunology. Shape translational biomarker frameworks and target identification strategies using large-scale omics, clinical data, and competitive intelligence to de-risk development and inform clinical decisions.

Pfizer £230,900 – £384,800 pa

Senior Director, Targets and Mechanisms Solutions

Leads the strategic direction and product management of AI-driven Targets and Mechanisms platforms within Pfizer’s R&D ecosystem. Oversees global teams delivering scalable, data-centric solutions that integrate omics, clinical data, and AI to identify and validate therapeutic targets across oncology, vaccines, and immunology. Drives innovation through advanced data pipelines, predictive analytics, and cross-functional collaboration with research and digital technology teams.

Pfizer

Research Pipeline Project Manager

Lead and coordinate cross-functional research pre-clinical pipeline projects, shaping strategies, removing barriers, and driving delivery across discovery stages. Work closely with scientists, clinical teams, and external collaborators to accelerate milestones while maintaining quality and safety. Focus on governance, risk resolution, and continuous improvement in ways of working to support GSK's R&D ambitions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Principal Scientist, Bioanalytical & Molecular Assays

Lead the development and validation of molecular assays including RT-qPCR, dPCR, and NGS for clinical biomarker programs across Moderna's therapeutic pipeline. Drive end-to-end assay lifecycle management, ensure regulatory compliance with GCLP standards, and collaborate with cross-functional teams to deliver high-quality genomic data. Mentor scientists and integrate advanced analytics and AI-enabled tools to accelerate discovery and translational research.

Moderna Oxford, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Manager

Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across regions. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on strategic planning, regulatory intelligence, and process innovation within a patient-first framework.

GSK United Kingdom

Executive Medical Director, Clinical Development Lead - Oncology

Leads clinical development strategy for oncology assets, defining the scientific narrative and benefit-risk framework across the lifecycle. Acts as the primary clinical authority, shaping strategic direction and governance decisions while leveraging AI and advanced analytics to accelerate development. Represents Clinical Development in internal and external forums, including regulatory interactions and alliance partnerships.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

Associate Director, Device Lead

Lead the technical ownership and global delivery of medical device platforms within GSK's manufacturing network, ensuring compliance with regulatory standards and driving innovation in device technology. Collaborate across R&D, supply chain, and quality functions to manage device lifecycle, technology transfer, and risk. Work with suppliers and internal teams to optimize manufacturing processes and support combination product development.

GSK United States £142,725 – £237,875 pa

Associate Director, Device Lead

Lead the technical ownership and lifecycle management of medical device platforms within GSK's global supply chain, ensuring regulatory compliance, technology transfer from R&D, and robust supply strategies. Drive innovation in drug delivery devices and combination products while collaborating across global teams on quality, manufacturing efficiency, and risk management. Serve as the primary technical interface between device suppliers and internal MSAT teams.

GSK £142,725 – £237,875 pa

Associate Director, Device Lead

Lead technical strategy and lifecycle management for drug delivery devices across GSK’s global manufacturing network, ensuring regulatory compliance, supply robustness, and innovation in device design and manufacturing processes. Serve as the primary technical liaison between device suppliers and internal MSAT teams, driving technology transfer, risk management, and continuous improvement initiatives. Focus on quality by design, digital data management, and sustainable manufacturing within a regulated GMP environment.

GSK £142,725 – £237,875 pa

Associate Director, Device Lead

This role leads the global technical ownership of drug delivery device platforms, ensuring robust supply, regulatory compliance, and lifecycle management across GSK's manufacturing network. The individual will act as the primary technical interface with device suppliers, drive innovation in device technologies, and support technology transfer from R&D to commercialization. Key responsibilities include risk management, process optimization, and ensuring adherence to global medical device regulations and quality standards.

GSK £142,725 – £237,875 pa

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading clinical development strategy for oncology, specifically lung cancer, providing medical oversight across trial design, safety monitoring, and data interpretation. The Senior Medical Director will guide cross-functional teams, engage with external experts, and contribute to regulatory submissions, ensuring patient-centred, scientifically rigorous development. Based in the UK with hybrid working, the position plays a key leadership role in advancing GSK’s oncology pipeline.

GSK Stevenage, United Kingdom PLN 593,250 – PLN 988,750 pa

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading clinical development in oncology, with a focus on lung cancer, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and mentor junior medical staff within a global matrix team. The position emphasizes strategic input, external scientific engagement, and integration of clinical insights to advance therapies for high unmet need.

GSK Switzerland

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, guides cross-functional teams, and represents the programme in regulatory and scientific forums. Based on-site with a future relocation to Cambridge, UK, the position emphasizes strategic clinical leadership within a global biopharma environment.

GSK

On-site Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, contributes to regulatory engagements, and mentors medical teams within a cross-functional environment. The position integrates physician expertise into clinical strategy and external scientific forums, focusing on advancing care in high unmet need cancers.

GSK

On-site Permanent