Principal Eng, Mechanical

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

•        "Contributes to the definition of product /design requirements, electronic system architecture development, design and implementation of electronic circuits, test of circuits and systems and the documentation and release of designs.

•        Contributes through demonstrated hands-on participation with teams. Accountable for direct production of project deliverables.

•        "An active and engaged member of Design Review Teams.

•        Ensures inclusion of inputs into product and technical design reviews from all cross functional stakeholders."

•        Ensures successful integration of Mechanical design entities with Electrical and consumable components.

•        "Contributes to design concepts and research methodologies that meet current and future customer & business needs for a product or process domain area.

•        Completes deliverables related to design of systems and sub-systems related to the overall mechanical architecture."

•        "Performs in-depth Mechanical engineering analysis and calculations.

•        Resolves competing constraints between interrelated functions (engineering, purchasing, manufacturing, regulatory, marketing, etc.) required to deliver the product to market."

•        Generates and/or improves Mechanical and electro mechanical designs that are optimized for production, reliability, regulatory compliance and cost.

•        Transitions products to manufacturing and ensures robust products and manufacturing processes and ensures right DHF documentation and DMR for manf. builds.

•        Executes protocols and testing required to validate the safety and effectiveness of the design(s).

•        "Develops and maintains an effective and collaborative working relationship with internal and external development partners.

•        Experience working with regulatory bodies like UL, TuV, ITT. "

•        "Recognized within the immediate team for technical and/or process expertise as evidenced by solicitation for input on a variety of issues.

•        Proposes and drives solutions to complex technical problems.

•        Understands and contributes to resolution of competing constraints among inter-related functions (e.g. engineering, manufacturing, regulatory, marketing) required to deliver products to market.

•        Leads the troubleshooting and problem solving efforts related to Mechanical aspects of devices and associated systems.

•        Leverages knowledge of technology, process, and/or therapy domains to drive solutions and product design realization.

•        Able to apply technical risk mitigation tools and execute mitigation strategies to ensure optimal results."

•        Engaged and respected within the team, for example may act as the leader for a subsystem for products of high complexity, as PDO, LSD, for products of simple to moderate complexity or as a subject matter expert on technical problems.

•        Participates as a member of cross functional teams and/or integrates cross functional inputs to delivery of a project of moderate technical and strategic complexity. May integrate technical development schedules for those products or subsystems, provided as input to the full cross-functional project schedule.

•        Contributes to intellectual property initiatives for a program. May hold patents that secure a competitive advantage for our products and/or assist with freedom to operate assessments for our products.

•        Creates and communicates design/test plans, tasks, deliverables and status. Manages time and resources to meet committed schedule milestones.

•        "Strong expertise in implementing the standards / regulatory requirements and testing it

•        Demonstrates awareness of FDA, ISO and IEC design control procedures, regulations and standards within area of responsibility/expertise and participates in external / internal audit as auditee / SME"

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

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