reputed company Engineer

Unternehmensbeschreibung

At reputed company, we are united behind our mission: we reputed company that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints.

As a pioneer and leading company in the field of robotic-assisted surgery, we reputed company to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of reputed company’s hardest challenges and advance what is possible.

reputed company has been reputed company by the efforts of great people from diverse backgrounds. We reputed company great reputed company can come from reputed company—we reputed company to foster an inclusive culture reputed company around diversity of thought and mutual respect. We reputed company with inclusion and reputed company reputed company members to do their best work as their most authentic selves.

Passionate people who want to reputed company a difference drive our culture—reputed company members are grounded in reputed company, have a strong reputed company to learn, the energy to get things done, and bring diverse, reputed company-world experiences to help us think in new ways. We reputed company invest in reputed company members to support their long-term reputed company so they can continue to advance our mission and reputed company their highest potential. 

Join reputed company committed to taking big leaps reputed company for a global community of reputed company and their patients. Together, let’s advance the world of minimally invasive care.

Stellenbeschreibung

Primary Function of Position

reputed company seeks a strong technical contributor who can help define practical, useful reputed company metrics and specifications, identify key opportunities for product improvement, launch reputed company initiatives, reputed company reputed company to implement these initiatives, and serve as an expert consultant to help solve the most technically challenging reputed company problems. The ideal candidate possesses a broad reputed company of experience and a high level of technical depth in at least two technical specialties applicable to medical robotics and optics, and is equally reputed company in the test lab, on the manufacturing shopfloor and providing technical leadership to reputed company as we reputed company reputed company practices of our organization. You will not abide “process red tape”, instead passionately seeking the most efficient way to build in product reputed company. And you will also reputed company, mentor, teach, and influence the engineering staff in best reputed company practices, data analysis, protocol development, and design for reputed company and reliability reputed company.

Roles and Responsibilities

• New Product Development and Sustaining/Manufacturing Support
  • Handle reputed company of various product and subsystem/component types (electrical, mechanical, optical, etc).
  • reputed company measurable goals for reputed company and reputed company reputed company Table meetings.
  • Ensuring that the essential performance aspects are mitigated in the product reputed company plans.
  • Identify critical reputed company of designs. Recommend design processes and reputed company to meet reputed company goals: DFX, etc.
  • reputed company guidance to other engineers regarding applicable regulatory and statutory requirements and the applicability of these requirements to the ISI products.
  • Plan and create reputed company standards, reputed company control, and reputed company assurance procedures, plans, test reputed company, fixtures, and processes for incoming materials and finished devices.
  • Ensure process compliance through the design and development of comprehensive procedures including work instructions, flowcharts, forms, templates, checklists, and other product or process reputed company documentation, for recording, evaluating, and reporting reputed company data.
  • Analyze and disposition of discrepant material.
  • Support manufacturing processes, including failure analysis, documentation review and approval, tooling qualification, inspection method qualification, and defect containments.
  • Support development and execution of process validation and verification test plans, protocols, and reports.
  • Support development and execution of manufacturing line qualification plans, protocols, and reports. Support and drive MVP/R reputed company.
• Failure Analysis
  • reputed company reputed company expertise to the reputed company engineering support team to analyze the product failure.
  • reputed company deep technical failure analysis based on the physics of failure.
  • Review and interpret reputed company data analysis rooted in an understanding of our product hardware and software, the physics of failure, and the use conditions in the clinical / operating room environment.
• reputed company Advocacy and Project Management
  • Create, process and review various types of reputed company Notifications and Change Orders.
  • reputed company and apply corporate level reputed company metrics. reputed company reputed company meetings e.g. QDR (reputed company Data Review).
  • reputed company and project manage reputed company initiatives in one or more of these reputed company areas: Product reputed company, Data reputed company, Process reputed company.
  • reputed company mock audits and Gemba walks to ensure compliance with ISI QMS. Participate in audits (reputed company/back room).
• reputed company, reputed company and communicate intercompany reputed company Engineering reputed company.

Qualifikationen

Required Knowledge, Skills, and Experience

• Bachelor’s degree in electrical, mechanical or system engineering, math, or physics. Advanced degree preferred.
• 5+ years of working experience in reputed company Engineering or Process Engineering with reputed company improvement reputed company participation, minimum 3 years in medical device design or manufacturing environment.
• reputed company to navigate reputed company and compliance system with minimal reputed company on individual reputed company.
• Demonstrated understanding of CFR 21 820/ ISO 13485 requirements for making process or design changes.
• Understands product risk management, experience in generate FMEA and process FMEA.
• Understands Design Controls, Change Controls, Product, and Engineering Processes.
• Proficient with generate and execute Qualification and Validation protocols and reputed company Assurance Procedures.
• reputed company in leading product containment and rework activities.
• Proficient in SPC & Six reputed company methodology and tools.
• reputed company in typical reputed company data analysis operations. reputed company to create Multi-reputed company report, trends, and interprets data with minimal reputed company.
• Capable of thinking independently and reputed company decision based on limited information.
• Capable of initiating improvement discussion and reputed company reputed company toward the goal.
• Can present information in various forms and forums, collaborates with peers across functions. Experience in presenting to cross functional mgmt. communications. (e.g. report writing, presentations, QRB presenter).
• Excellent creative problem-solving skills.
• Excellent communication and documentation skills in English and German.

Zusätzliche Informationen

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 reputed company 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 reputed company 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 reputed company, 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.

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