Lead global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Partner with cross-functional teams and external collaborators to generate regulatory-grade evidence and shape development strategies. Drive scientific dissemination through publications, regulatory submissions, and international conferences.
Leads global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and safety teams, manages external collaborations, and drives scientific dissemination through publications and regulatory submissions. Focuses on strategic epidemiological planning and mentoring junior staff within a matrixed R&D environment.
Leads the technical architecture and development of Pfizer's global Medical Insights platform (InsightXplorer), translating regional and business needs into scalable technical solutions. Drives innovation by evaluating new data sources, AI methods, and analytics approaches, and collaborates across global teams to deliver a reliable, evolving platform. Works at the intersection of engineering, product, and stakeholder engagement to ensure technical decisions deliver scientific and business value.
Leads the technical architecture and development of Pfizer's global Medical Insights platform, InsightXplorer, translating business and regional needs into scalable technical solutions. Drives innovation by evaluating new data sources, AI methods, and analytics approaches for integration into the platform. Works cross-functionally to align engineering, data governance, and stakeholder requirements while enabling change management and platform adoption.
Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.
This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.
You will design and build a full-stack AI platform that connects scientists directly to experimental results, owning the system architecture from model endpoint to user interface. The role involves rapid prototyping, close collaboration with in-house scientists, and shaping both product and technology for a novel scientific discovery platform. You'll start as an individual contributor with a path to lead technical direction.
Lead complex mathematical and simulation-based modelling projects in bioprocessing and life sciences within a high-growth, well-funded start-up. Work autonomously on advanced technical challenges with opportunities for long-term career development in a remote-first environment. Collaborate with a growing team focused on accelerating technology through advanced modelling.
This role involves leading the design, testing, and verification of electromechanical systems in medical devices, with a focus on improving reliability and supporting technology transfer to production. The engineer will conduct root cause analyses, optimize system performance, and lead cross-functional design reviews. Work spans system integration, validation, and documentation within a regulated healthcare technology environment.
The role involves leading technology transfer activities for diagnostic products, bridging R&D and manufacturing teams. You'll coordinate process transfers, manage technical documentation, support validation, and ensure compliant, scalable production. The position focuses on problem-solving during transfer projects and driving continuous improvement in a regulated environment.
Lead and maintain the Quality Management System (QMS) in a regulated diagnostic manufacturing environment, ensuring compliance with ISO standards and audit readiness. Drive quality documentation, process improvements, and cross-functional collaboration with technical and operations teams. Play a key role in upholding product safety and quality within a growing, innovative business.
This role involves leading pharmacovigilance and safety science activities across Roche’s medicine portfolio, with responsibilities spanning signal detection, risk management, and safety reporting. The individual will contribute to clinical development strategies, oversee post-market safety assessments, and ensure compliance with global regulatory standards. Working within a hybrid model in Welwyn, the position requires strong scientific analysis, leadership, and cross-functional collaboration in a regulated environment.
This role involves leading end-to-end enterprise sales cycles to acquire new clients in the pharmaceutical and biotech sectors. The Senior Account Executive will engage with scientific, technical, and executive stakeholders to position Helical’s AI-native biology platform, translating complex technology into tangible value. The position offers a strategic opportunity to shape the commercial strategy of an early-stage company at the intersection of AI and drug discovery.
Lead a computational drug discovery team focused on structure- and fragment-based design, integrating AI/ML, cheminformatics, and advanced simulation methods into multidisciplinary drug discovery programmes. Drive computational strategy while maintaining hands-on involvement in projects from hit identification through to candidate nomination. Collaborate closely with medicinal chemistry, structural biology, and biophysics teams to deliver innovative therapeutics.
Leads the operational delivery of high-impact, global R&D projects within a cross-functional biotech environment. Focuses on strategic planning, budget and timeline management, risk mitigation, and stakeholder reporting. Provides mentorship to junior project management staff and ensures robust project execution across drug research, development, and manufacturing.
