Engineer

In this role, you have the opportunity to design, develop and maintain Intravascular Ultrasound Consoles and Patient Interface modules. As a member of an international cross-functional team, you work closely with hardware engineers, product industrialization engineers, procurement experts, and external partners. You are responsible for planning and tracking Mechanical design, ensures risks are mitigated, and communicated to stakeholders. You will ensure that your design is consistent with the higher-level architecture and requirements. Major parts are plastic molding parts, sheet metal parts, and electromechanical assemblies.

Your responsibilities:

Lead design and detail of components and systems, including conducting predictive analysis and calculations.
Select materials and processes appropriate for those designs
Lead prototypes creation plan and execution.
Write/review test protocols, conduct tests, analyze data, and report results.
Successfully interact with associates in other departments, such as Manufacturing Operations, Procurement, and engineering staff, to achieve project and product objectives.
Develop new test methods and tools as necessary. Specify, acquire, and maintain lab equipment.
Operate lab instruments such as micrometer, tachometer, manometers, flow meters, tensile and compression testers, data acquisition systems, environmental chambers, and computer programs.
Be a highly motivated, self-disciplined, open-minded individual possessing hands-on skills.
Requirements detailing, design specification preparation, implementation, test, and integration of Unit per the higher-level Requirement and - Design specifications/architectures.
Ensures the mutual consistency and efficient integration of the separate modules in modular, easy-to-maintain units that meet the product specification.
Understands and communicates the consequences of their design on the architecture.
Determines the Unit interfaces (HW/SW) in close consultation with relevant disciplines.
Ensures that there is proper documentation for his/her design.
Keeps abreast of technical developments in own field through study of the literature and technical contacts, and propagates it.
Defines, execute, and take the lead in concept and feasibility studies with a limited scope to investigate the usability of new technologies.
Contributes to technology roadmaps and other strategic-related activities.
Takes technological or process-related improvements initiatives within the scope of at least the mechanical development group.
Contributes to the Work Breakdown Structure/ the planning process of his/her area.
Draws up personal schedule and reports on progress.
Inspires team members to get the job done.
Performs work in line with the processes that have been agreed in the department.

To succeed in this role, you should have the following skills and experience:

Bachelor s or master s degree in precision engineering, mechanical engineering, medical engineering, or equivalent.
In-depth knowledge and 6-8 years of experience in the development of mechanical design
Experience in creating design concepts and mechanical designs of complex parts or assemblies.
Strong knowledge and experience in CAD/CAE. such as SolidWorks
Experience in metal or plastic crafts (drilling, milling, etc.) would be appreciated
Good basics in physics
Good knowledge and experience with gate staged development governance, ideally familiar with
ISO 13485 or FDA-regulated development processes.
knowledge of medical requirements and regulatory standards is beneficial (such as IEC 60601-1)
Capability to interact in cross-functional teams
Outstanding commitment, being innovative and adaptive