Senior Regulatory Affairs Manager, SaMD and GxP, United Kingdom We are looking for a Senior Regulatory Affairs Specialist to support the regulatory strategy and compliance activities for AI-enabled software products used within clinical and healthcare environments. This position will play a key role in ensuring products meet international regulatory and quality standards across the UK, EU and US markets. The role will involve leading regulatory submissions and maintaining compliance for Software as a Medical Device (SaMD) and AI-based technologies, while working closely with cross-functional teams including Quality, Engineering, Product, Clinical Operations and Data Science. You will provide regulatory guidance throughout the software development lifecycle, including validation activities and risk management processes. Key responsibilities include: Developing and implementing regulatory strategies for software and AI-driven medical technologiesSupporting global regulatory submissions and interactions with notified bodies, auditors and regulatory authoritiesEnsuring compliance with relevant standards and regulations including ISO 13485, IEC 62304, ISO 14971 and AI/ML guidanceReviewing technical documentation, risk management files and validation documentationSupporting audits, inspections and quality management activitiesMonitoring regulatory developments and advising internal teams on compliance requirements The ideal candidate will have: Significant experience within ..... full job details .....