Sr. Engineer Disposables

Vantive: A New Company Built on Our Legacy

Since last year, Baxter has been on a journey to separate our Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. 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 are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.

*Completion of the proposed sale of Vantive to funds managed by the Carlyle Group is subject to receipt of customary regulatory approvals and satisfaction of other closing conditions.

• Development of mechanical Fluid control systems by designing and conducting research programs; applying principles of mechanics, thermodynamics, hydraulics, heat transfer, and materials.
• Ensures successful integration of mechanical design entities with electrical and consumable components.  Contributes to troubleshooting and problem solving efforts related to mechanical aspects of the design and interfaces with other design constituents.
• Contributes to development and documentation of mechanical systems architectures.
• Able to effectively transition products to manufacturing and ensure robust products and manufacturing processes.
• Generates and/or improves Plastic Component/System designs that are optimized for production, reliability, regulatory compliance and cost.
• Performs in-depth mechanical engineering analysis and calculations, Risk Analysis.
• Resolves competing constraints between interrelated functions (engineering, purchasing, manufacturing, regulatory, marketing, etc.) required to deliver the product to market.
• Defines protocols and conduct the necessary testing required to validate the safety and effectiveness of the design(s).
• Develops and maintains an effective and corroborative working relationship with internal and external development partners. 
• Executes protocols and testing required to validate the safety and effectiveness of the design(s).
• Troubleshooting and problem solving efforts related to mechanical aspects of devices and associated systems/subsystems.
• Creates and communicates design/test plans, tasks, deliverables and status. Manages time and resources to meet committed schedule milestones.
• A demonstrated track record in Plastic component Design, preferably medical devices or other highly regulated products.
• In depth knowledge of the regulatory environment for Design, Develop and Manufacture of Medical products.
• Knowledge of standards such as IEC 60601, UL, ANSI, ASTM standards.
• Experience working with regulatory bodies like UL, TuV, ITT
• Understanding of the Healthcare regulatory environment and country regulations
• Demonstrated strong analytical and problem solving skills
• Success in working with multifunctional, global teams.
• Excellent interpersonal/communication/influencing skills required

Reasonable Accommodations

Baxter 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.

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