This role involves managing and maintaining quality processes, ensuring compliance with regulatory requirements, and supporting inspection readiness across CSL's global affiliates. You will collaborate with cross-functional teams to implement quality initiatives and improve systems.
This role involves managing and improving quality systems across CSL's European affiliates, ensuring compliance with regulatory requirements. Responsibilities include coordinating inspection readiness, maintaining quality KPIs, and supporting global quality initiatives. The position requires strong knowledge of pharmaceutical regulations and quality systems, with a focus on continuous improvement and cross-functional collaboration.
Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.
Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.
This role involves partnering with the Head of Portfolio Decision Sciences to support the R&D portfolio in the Respiratory, Immunology & Inflammation (RI&I) and broader Pharmaceutical pipeline. Responsibilities include conducting economic analyses, guiding project teams, and providing strategic recommendations to senior leadership for portfolio investment decisions. The role requires extensive R&D experience and a strong background in portfolio management.
This role involves partnering with the Head of Portfolio Decision Sciences to support the R&D portfolio in Respiratory, Immunology & Inflammation (RI&I) and broader pharmaceuticals. Responsibilities include conducting economic analyses, probabilistic evaluations, and strategic assessments to guide investment decisions and enhance the pipeline. The role requires strong data-driven decision-making skills and collaboration with cross-functional teams.
This role involves developing and executing HEOR and HTA strategies for Novartis' Immunology portfolio, ensuring payer and HTA evidence requirements are integrated into clinical development plans. You will partner with various teams to maximize asset value and translate complex evidence into compelling value stories for healthcare decision-makers.
The Vendor Program Head leads the vendor strategy and management for clinical development programs within a specific disease area. Key responsibilities include overseeing vendor execution, building high-performing teams, and ensuring alignment with development priorities and quality standards.
Perform on-site installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide technical support and troubleshooting for complex laboratory equipment, working closely with lab managers and technicians. The role involves regular weekend work and extensive customer interaction across a diverse range of clinical environments.
This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings. The engineer will troubleshoot on-site, provide technical support, and liaise with laboratory staff. Full product training is provided, and the role requires some weekend work due to a five-day-in-seven schedule.
The Shift Laboratory Analyst will work in a high-throughput laboratory, preparing and analysing samples, performing wet chemical and instrumental analysis, and maintaining laboratory equipment. The role involves supporting quality activities and technical projects, with a focus on accuracy and adherence to procedures.
Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...
This role involves taking ownership of engineering workstreams across medical device and combination-product development projects, coordinating technical activities with engineering, quality, suppliers, and manufacturing teams. Responsibilities include product development, NPI, verification, validation, industrialisation, and manufacturing transfer, with a focus on technical problem-solving and documentation.
The role involves end-to-end management of clinical trials within a fast-paced, AI-driven drug discovery environment. The Senior Clinical Trial Manager will lead cross-functional teams, oversee trial start-up through close-out, ensure compliance with ICH/GCP standards, and integrate AI innovations into clinical operations. Key responsibilities include vendor and budget management, clinical documentation, data oversight, and supporting regulatory readiness and audits.
Develop and optimise cutting-edge AI models at the intersection of machine learning and drug discovery, translating research into scalable, production-ready systems. Work on foundational models like Diffusion networks, Transformers, and GNNs, building robust infrastructure and data pipelines while collaborating closely with scientists. Focus on advancing a digital biology platform to accelerate rational drug design across multiple therapeutic areas.
