Philips Senior System Engineer - Interventional Hemodynamic Solutions 

Germany, Hesse 

580655260

Senior System Engineer - Interventional Hemodynamic Solutions
Job Description

As a Senior System Engineer, you'll play a crucial role in the development of the Philips Interventional Hemodynamic System. This medical system is pivotal in assessing and analyzing a patient’s hemodynamic condition during Interventional Cardiac Procedures.

Your Role:

• Oversee the requirements and risk management of the (released) system or system component within our Hemo portfolio.

• Manage safety, privacy, and security risks associated with the designated system or component.

• Coordinate, in close collaboration with the system architect, the interfaces between various hardware and software components comprising the Philips Hemo System.

• Manage interfaces between the Philips Hemo System and external components or systems.

• Take ownership of the overall design and integration of a system or system function throughout multiple stages of the product life cycle, mainly focusing on hardware aspects such as EMC, risk management, reliability, and obsolescence, aligned with the product architecture defined by the system architect.

• Develop the design specifications for external components in collaboration with suppliers.

• Define the technical concept, mapping dependencies, and implementing constraints originating from legacy, regulatory, and relevant cross-functional areas for the designated system or function.

• Lead fault-finding sessions and develop solutions for software/hardware issues identified in our released products (based on field feedback) or during the implementation, integration, and testing phase of a product realization project.

You're the right fit if:

• You hold a Master's degree in electrical, mechanical engineering, or related fields.

• Possess a minimum of 5 years of experience in system design, with a strong emphasis on hardware, Experience with software as part of a system is considered a plus.

• Demonstrate proficiency in regulated industries, particularly in the medical device sector, with a solid understanding of relevant standards and compliance requirements.

• High commitment to quality, with demonstrated expertise in leading fault-finding sessions using advanced methodologies.

• Skilled in collaborating in small cross-functional teams and (external) development organizations.

• Results-oriented and practical, with the ability to quickly adapt to new areas and challenge conventional approaches.

• Team player with excellent communication skills, with fluency in English and Dutch preferred, enabling effective stakeholder influence.

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