• You own the fraud P&L. Payout rate, chargeback rate, approval rate, false-positive rate — across the business, these are yours. You're the one who can explain every movement and who's accountable for the trend line. • You won't just run the team; you'll build a strong second line of leadership beneath you and develop the people in it, so the function stays sharp whether or not you're in the room. • You own the fraud-reduction roadmap. You decide what we build versus buy, where we invest, and how the multi-product fraud program is designed — then you make sure it actually ships. • You own the commercial and strategic relationships with our fraud-prevention partners. RFPs, champion-challenger tests, SLAs, and the negotiations themselves sit with you. • You're the operational partner to Product, Engineering, Finance, and Legal. When the business builds something new, you make sure fraud risk is designed in from the start — not patched in after the first loss. • You own our risk-side regulatory and compliance obligations — PSP requirements, KYC, and law-enforcement requests — and make sure we're defensible as we scale across markets. • You're the top escalation point for the hardest risk calls, and you represent Risk & Fraud in cross-functional and leadership forums with structure, data, and a clear point of view.

• Lead and coordinate all risk management activities according to ISO 14971, ISO 13485, MDR and annex XVI. • Plan, prepare and perform risk management for medical devices and aesthetic products according to project phases following all relevant internal procedures, processes, and external requirements for development products. • Represent Risk Management on assigned development projects. • Establish risk acceptance criteria for individual residual risks and the overall residual risk for specific devices in development and for legacy devices • Maintain a close link to the Human Factors / Usability Engineering process to meet the needs and ensure the safety of all users and patients. • Support creation of device design specifications to ensure that risk control measures are appropriate. • Monitor that risk control measures have been implemented, verified, and validated. • Maintain knowledge of current Company policies, standards and guidelines as well as industry practices, regulatory requirements, and other relevant information. • Ensure harmonized approaches to risk management across projects. Communicate with Research and Development team members on other projects to share lessons learned and ensure use of common tools and ideas within the team. • Ensure that the risk management process incorporates all relevant data from the Design Authorities e.g., Design FMEAs, Security Risk Analysis, Use-related risk analysis, formative human factors evaluations and human factors validation studies. • Ensure that risk management reports are prepared in a timely manner and in accordance with ISO 14971 and applicable Company SOPs and guidelines and are adequate for inspection by notified bodies and other relevant authorities. • Present project-specific risk management activities at regulatory body inspections and internal audits. • Work cross-functionally with other global functions: e.g., Global Marketing, Global Regulatory Affairs, Clinical Affairs and Manufacturing. • Support a good link between risk management during development and risk management for marketed products. • Ensure that all hazards associated with a medical device and aesthetic products are identified, the associated risks are estimated and evaluated and that these risks are controlled; monitors that these risk controls are implemented, verified and validated. • Assures that Company quality and compliance standards and applicable government regulations are met by means of independent risk management for medical devices under development. • Performs risk management in medical device and aesthetic projects and assists medical device sites in ensuring that risk management is performed in sufficient detail and in a timely manner for new device introductions and regulatory agency inspections. • Has overall responsibility that medical devices and aesthetic products are designed to be safe, effective and in compliance with the applicable regulations worldwide.

• Coordinar la planificación y ejecución de cambios en entornos PRE, asegurando cumplimiento de ventanas operativas y control de riesgos. • Establecer y mantener la gobernanza de entornos, garantizando estabilidad operativa y trazabilidad de actividades. • Facilitar y liderar procesos de CAB (Change Advisory Board), asegurando la correcta evaluación, aprobación y comunicación de cambios. • Supervisar despliegues y actividades técnicas en coordinación con equipos de infraestructura, aplicaciones, testing y soporte. • Gestionar riesgos operativos, incidencias y dependencias en plataformas tecnológicas complejas. • Asegurar la comunicación efectiva entre equipos y stakeholders durante ciclos de cambio y eventos críticos.

Role Description Aon are currently recruiting Risk Settlement Group Consultants across the country (work location is flexible). As a Risk Settlement Consultant at Aon, you will be a member of our 70–strong Risk Settlement Group, which has a uniquely diverse range of experts and specialist sub-teams. Some of your responsibilities will include: - Support to transaction advisers on a range of settlement transactions across the pension risk transfer market (including buy-ins, buy-outs, wind-ups, longevity swaps, and consolidation/capital solutions) - Take responsibility for the running of transactions, ensuring they are completed on time and on budget and develop relationships with transaction stakeholders. - Help advise clients on their strategic ‘Journey to Settlement’, including preparation for approaching the settlement market and feasibility. - Support on new business opportunities and initiatives both internally and externally. - Leverage your knowledge of the settlement market to help deliver settlement solutions for our clients. - Support marketing initiatives and media engagement, including our annual marketing campaign and our dedicated risk settlement conference. - Help to develop new strategies and propositions within the Risk Settlement Group. - Coach, mentor and support direct and indirect reports. Qualifications - Track record of delivery on settlement transactions - Industry experience coupled with sound technical capability - Strong communication and interpersonal skills - Self-motivating and ambitious - Able to encourage and develop colleagues, and work well within diverse teams - Whilst having an eye for detail, also capable of considering wider matters Benefits - Comprehensive benefits package - Encouragement of an inclusive workforce - Agile environment for managing wellbeing and work/life balance - Two “Global Wellbeing Days” each year - Variety of working style solutions - Continuous learning culture - Reasonable accommodations for individuals with disabilities