Clinical Applications Engineer Reprocessing (mwd)

Intuitive; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading medical technology company in Germany seeks a Clinical Applications Engineer - Reprocessing to serve as a technical liaison for reprocessing solutions. This role involves managing exploratory research, working with diverse teams, and ensuring compliance with local regulations. The ideal candidate will have a Bachelor's degree in science or engineering, strong communication skills, and be fluent in both English and German. A willingness to travel up to 60% is essential for this full-time position.

Leistungen

Flexible work arrangements

Professional development opportunities

Health insurance benefits

Qualifikationen

• 4+ years of experience in the medical industry with a focus on customer needs.
• Experience working with cross-functional teams across different time zones.
• Fluency in English and German.

Aufgaben

• Develop and implement project plans for exploratory research.
• Conduct site assessments to understand local reprocessing needs.
• Collaborate with teams to prioritize expansion targets.

Kenntnisse

Medical procedures knowledge

Project management

Strong communication skills

Client relationship management

Ability to travel

Ausbildung

Bachelor's degree in science or engineering

Tools

SolidWorks

Laboratory experience

Jobbeschreibung

Primary Function of Position

The Clinical Applications Engineer - Reprocessing serves as a technical liaison for Intuitives endoluminal reprocessing solutions across new and existing markets. This position is critical for enabling the successful deployment and sustainability of Intuitives endoluminal reprocessing programs in diverse healthcare settings.

Working cross-functionally with commercial teams reprocessing trainers engineering and external partners this role ensures that reprocessing solutions are technically sound compliant scalable and aligned with regional and customer-specific needs.

Roles and Responsibilities

• Execute exploratory reprocessing research programs to support expansion into new regions.
• Develop and implement project plans for research programs.
• Collaborate with commercial clinical and market teams to prioritize expansion targets.
• Engage stakeholders (hospital admins clinical staff) and conduct site assessments to understand local reprocessing needs.
• Deliver tailored information sessions and ensure compliance with local regulations.
• Monitor outcomes and share learnings with leadership for continuous program improvement.
• Serve as the voice of the customerduring early-stage product development by gathering feedback from end users and external partners identify customer challenges and advocate effective solutions.
• Support validation and launch strategies including hands‑on field training and feedback collection.
• Review documentation as Subject Matter Expert to ensure clarity and compliance.

Qualifications

Required Knowledge, Skills, and Experience:

• Minimum bachelors degree in science engineering or a related field or equivalent relevant experience.
• Demonstrated experience or strong interest in medical procedures and reprocessing with applicable certifications.
• Minimum 4 years of industry experience with a proven track record of translating customer needs into actionable design insights.
• Experience working directly with customers to articulate the value and potential of new medical technologies and thrives in a high-energy fast-paced and customer-facing environment.
• Demonstrated success collaborating with international cross-functional teams across multiple time zones to ensure effective communication and coordinated execution.
• Experience navigating complex or high-tension situations aligning stakeholders toward effective forward-looking solutions.
• Excellent written and verbal communication presentation and interpersonal skills.
• Acts as a Medical Device Consultant (Medizinprodukteberater) in Austria and Germany after appropriate training as per legal requirement and provide guidance insight and support in the proper handling of Intuitive medical devices.
• Willingness and ability to travel up to 60% often on short notice to support accounts across multiple geographies.
• Fluent in English and German.

Additional Information

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 Mitarbeiter 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 (Hinweis: Das Lizenzierungsverfahren der Regierung kann 3 bis 6 Monate dauern) oder (ii) einen Technologiekontrollplan (TCP) implementieren muss (Hinweis: verlängert den Einstellungsprozess in der Regel um 2 Wochen).

Für jede intuitive Rolle die Exportkontrollen unterliegt hängen die endgültigen Angebote vom Erhalt einer genehmigten Exportlizenz und/oder eines ausgeführten TCP vor dem Startdatum des potenziellen Mitarbeiters ab was flexibel sein kann oder auch nicht und innerhalb eines Zeitrahmens der den Einstellungsbedarf nicht unangemessen behindert. Gegebenenfalls werden die Kandidaten über die diesbezüglichen Anforderungen informiert und angewiesen

Remote Work

Yes

Employment Type

Full-time

Key Skills: Laboratory Experience,Vendor Management,Design Controls,C/C++,FDA Regulations,Intellectual Property Law,ISO 13485,Research Experience,SolidWorks,Research & Development,Internet Of Things,Product Development

Experience: years

Vacancy: 1