Senior Risk Manager Azurion Eye - AI, cloud, Sa(N)MD

Job description

Job Title Senior Risk Manager Azurion Eye - AI, cloud, Sa(N)MD Job Description Senior Risk Manager Azurion Eye - AI, cloud, Sa(N)MD As Senior Risk Manager within the Azurion Eye program, you own and continuously evolve the product risk management strategy across the complete product lifecycle. You ensure that AI-enabled, cloud-based, and connected medical solutions are developed and maintained in line with applicable safety, quality, and regulatory requirements. Your role: Lead product risk management activities from early concept and architecture through development, regulatory submission, post-market surveillance, and continuous software releases. Develop and maintain the Product Risk Management File in accordance with ISO 14971 and Philips QMS requirements. Lead hazard analyses, benefit-risk assessments, software risk analyses, and AI risk assessments. Define safety strategies for AI-enabled SaMD, SaNMD, cloud-native software, connected medical devices, and distributed services. Facilitate cross-functional risk workshops with Engineering, Clinical, Quality, Regulatory Affairs, and Product Management. Integrate risk management into Agile, DevSecOps, CI/CD, and software lifecycle practices. Use complaint data, software telemetry, clinical feedback, and AI performance monitoring to support product safety decisions. Support regulatory submissions, audits, CAPA investigations, field actions, and post-market surveillance. Coach development teams and promote a strong product safety culture. You're the right fit if: A Master’s or PhD in Biomedical Engineering, Systems Engineering, Software Engineering, Computer Science, or a related field. At least 8 years of experience in regulated medical device development. Extensive experience leading risk management for software-intensive medical devices. Experience with AI-enabled SaMD, connected healthcare systems, cloud-native software, and distributed architectures. Strong knowledge of ISO 14971, IEC 62304, IEC 82304-1, ISO 13485, IEC 81001-5-1, FDA QMSR, and EU MDR. Experience with cybersecurity risk management, regulatory submissions, audits, and post-market surveillance. Strong stakeholder management skills and the ability to influence cross-functional engineering teams. Excellent written and verbal communication skills in English Nice to have Experience with MLOps, computer vision, foundation models, or large language models. Knowledge of AI performance, bias, explainability, model drift, human oversight, and AI governance. Experience with Azure or AWS, Kubernetes, containerized applications, DevSecOps, and continuous software delivery. Knowledge of connected-device interoperability, including DICOM, HL7, and FHIR. Familiarity with FDA Good Machine Learning Practice and ISO/IEC 42001. Compensation & benefits Doing meaningful work should come with fair, transparent rewards. The base salary range for this role is €78187–€130312. We determine pay within the range using objective factors, like the skills the role requires, your relevant experience and the responsibility you'll have in this role, alongside internal equity and local market considerations. This role is eligible for 3% bonus, with your rewards linked to KPIs/company results. We’ll share the full approach with you during the interview process, so you can make a clear, informed decision. How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. About Philips Are you ready to do the work of your life to help the lives of others? Learn more about our business , discover our rich and exciting history and learn more about our purpose . If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care . #ImageGuidedTherapy