Spezialist Medizinprodukteaufbereitung AEMP (m/w/d)

Primary Function of Position: The Genesis I&A Consultant will provide customers with onsite, remote consulting and educational initiatives designed to implement and maintain Intuitive medical technology / instrument and accessories best practice solutions through standardization, efficiency, staff training, and cost containment. The Genesis I&A Consultant will also closely work with hospital key stakeholders as well as the Intuitive Ecosystem partners, including leadership, as well as with Sales, Advanced Failure Analysis, Marketing, Customer Services, and Tech Support to ensure that customers have the necessary tools to launch, optimize and sustain successful da Vinci and Ion programs. Roles and Responsibilities: Develop and maintain expertise in the following: Intuitive technology, I&A reprocessing, and troubleshooting Proper handling, care and use of Intuitive Instruments and Accessories Detailed knowledge of regulations, standards, and guidance in the area of reprocessing of reusable medical devices (ISO, MDR etc.) Independently manage assigned territory while effectively managing work time and schedule Conduct Genesis I&A Consultant and educational initiatives with Intuitive with strategically targeted customers. Provide in person and/or remote consulting and educational services to deliver value to the customer. Examples of services are staff training, consultation on program readiness, standardization, efficiency, and high return remediation. Support complex, extended customer engagements and collaborate with customers, as well as Intuitive commercial, service, and support teams to formulate multi-faceted, customized solution and recommendations based on hospital use patterns, processes, protocols, goals, and other feedback. Uncover customer needs and opportunities. Prioritize potential solutions and gain alignment with hospital key stakeholders to help implement recommendations. Track progress and communicate status to customer on a schedule identified within the recommendations. Align with sales and failure analysis partners on delivering customized customer assistance, as needed. Collaborate with internal and external stakeholders to define, measure, and optimize the quality, effectiveness, and efficiency of Genesis programs. Run reports and analyze data when needed to prepare for customer engagements. Support customer and internal facing Genesis and Intuitive events and conferences (both in-person and virtual). Promote collaboration with Genesis and cross functional teammates to establish and achieve Genesis implementation goals. Report customer complaints to appropriate internal parties as they are discovered. Ad-hoc tasks or duties assigned by management. Required Knowledge, Skills, and Experience: Experience in the AEMP environment and/or qualification as Technical Sterilization Assistant are required 5+ years of documented professional experience in healthcare/hospital management Detailed knowledge of regulations, standards, and guidance in reprocessing of reusable medical devices (ISO, MDR etc.) Experience or working knowledge of the use and/or reprocessing and regulations of complex medical devices, and excellent mechanical aptitude and problem-solving skills Proven ability to work effectively and drive results as part of a team Excellent communication and interpersonal skills with ability to present to varying group sizes Ability to excel in a high-energy, fast-paced environment Willingness to be flexible with work hours Master complexity – ability to plan, organize, and oversee highly complex and strategic assignments involving multiple teams and individuals Fluent in English and German is required Ability to travel overnight up to 70 % Wir schätzen jede Person in ihrer Individualität – unabhängig von Geschlecht, ethnischer oder sozialer Herkunft, Religion, besonderen Bedürfnissen, Alter oder sexueller Identität. Diskriminierung hat bei uns keinen Platz. Haftungsausschluss für US-Exportkontrollen : In Übereinstimmung mit den U.S. Export Administration Regulations (15 CFR §743.13(b)) können einige Positionen bei Intuitive Surgical US-Exportkontrollen für potenzielle Mitarbeitende unterliegen, die Staatsangehörige von Ländern sind, die derzeit einen Embargo- oder Sanktionsstatus haben. Bestimmte Informationen, die Sie im Rahmen der Bewerbung angeben, werden verwendet, um festzustellen, ob Intuitive Surgical (i) in Ihrem Namen eine Exportlizenz von der US-Regierung einholen muss (das Lizenzierungsverfahren der Regierung kann bis zu sechs Monate dauern) oder (ii) einen Technology Control Plan (TCP) implementieren muss (verlängert den Einstellungsprozess in der Regel um 2 Wochen). Für alle Positionen bei Intuitive, die Exportkontrollen unterliegen, steht ein endgültiges Angebot unter dem Vorbehalt, dass vor dem geplanten Eintrittsdatum eine genehmigte Exportlizenz und/oder ein vollständig ausgeführter Technology Control Plan (TCP) vorliegt. Das Eintrittsdatum kann dabei angepasst werden, sofern der Genehmigungsprozess den Einstellungsbedarf nicht unangemessen beeinträchtigt. Diese Position kann abhängig von den betrieblichen Anforderungen und/oder der Erfahrung der ausgewählten Kandidatin bzw. des ausgewählten Kandidaten auf einer anderen Jobstufe als hier angegeben besetzt werden. Die Vergütung richtet sich nach der Jobstufe sowie der Qualifikationen der Kandidatin bzw. des Kandidaten, selbstverständlich unter Berücksichtigung aller gesetzlichen Vorgaben.