Principal Eng, Systems

• The ideal candidate will leverage his/her exposure to embedded software and its interplay with electronics/hardware to support optimal system/product level realization for new products as well as sustenance of the existing products to deliver dialysis therapy.
• You join our Systems engineering function which is a part of the larger R&D organization and collaborate across functions (Software, Hardware, V&V, Digital) and sites globally (QA, RA, Clinical, Service, Mfg).
• The successful candidate will possess strong technical abilities, an excitement and energy for product development, and a passion for their work and the impact it has on extending lives and expanding possibilities.

Essential Duties and Responsibilities:

• As a member of cross-functional team, integrates cross functional inputs to delivery of a project of minor to moderate complexity.
• Product Requirements creation, analysis and management.
• System integration and testing.
• Leverages knowledge of technology, process, and/or therapy domains to drive solutions and product design realization.
• Contributes through demonstrated hands-on participation with teams. Accountable for direct production of project deliverables.
• Contributes to design concepts and research methodologies that meet current and future customer & business needs for a product or process domain area.
• Participates as a member of Design Review Teams.
• Ensures inclusion of inputs into product and technical design reviews from cross functional stakeholders.
• Proposes and drives solutions to technical problems.
• Engaged within the team. May act as the leader for a subsystem for products of minor to moderate complexity or as a subject matter expert on technical problems.
• Understands and contributes to resolution of competing constraints within assigned function (eg systems, electrical, software, or mechanical engineering) required to deliver products to market.
• Able to apply technical risk mitigation tools and execute mitigation strategies to ensure optimal results.
• Able to contribute to the program/project or the organization s technical strategy.

Desirable :

• Awareness of medical devices ISO and IEC design control procedures, regulations and standards.

Qualifications:

• bachelors or higher engineering degree in Electrical/Electronics, Bio-medical, or related discipline.
• Proven experience as a systems engineer or a similar role.
• Proficiency in relevant software & systems tools & techniques.
• Strong analytical and problem-solving skills.
• A demonstrated track record in electromechanical system development, preferably medical devices or other highly regulated products.
• Excellent communication and collaboration abilities.