Vantive: A New Company Built on Our LegacySince 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.SummaryAre you ready to take on a unique opportunity as a V&V leader?
Join our team at Baxter and be part of a world-class R&D organization dedicated to improving medical products.
We are looking for an individual with exceptional work behaviors to lead, when needed, the verification and validation activities of our innovative electromechanical medical product.
As the V&V leader, you will play a crucial role in ensuring the flawless performance and regulatory compliance of our productsYou'll follow all phases of V&V activities at system and sub-system level of our electromechanical medical products, from the impact analysis, through the definition of the test activities up to the preparation of all the documentation in line with the regulatory/standard requests and the QMS.What you'll be doingThe V&V activities include:Coordination of Sys V&V team as technical leaderVerification of technical requirementsValidation of intended use and user needsSafety system verification and compliance to 60601-2-16Risk Control Measures VerificationLabeling and Training material VerificationDevelopment of tool/test bench/test method for supporting test activitiesCollaboration on investigation, feasibility and root cause analysisActive participation in multi-functional and/or cross-sites teamsSupport on internal and external AuditManagement of instruments/toolsWhat you'll bringMaster's Degree in Electronic Engineering or Biomedical EngineeringISTQB certificate is preferred5+ years of experience working in R&D, in System V&V and experience with medical device products is preferredUnderstanding of medical device product design and regulatory processesKnowledge of applicable standards and regulations (FDA, ISO and IEC)Deep knowledge of Design Control and of Design Of ExperimentsFamiliarity with Electronic and Software instruments and tools used in V&V labFamiliarity with Statistical Analysis and Test Methods ValidationFamiliarity with system design, electronics, mechanical and software integrationExperience with LabView and Test Stand development is preferredAble to communicate optimally, both verbally and in writing, within an international and multi-site environmentTeam working approach, Problem-solving attitude and ability to organize and prioritize tasksReasonable AccommodationsBaxter 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.Recruitment Fraud NoticeBaxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information.
To learn how you can protect yourself, review our Recruitment Fraud Notice.150537#J-18808-Ljbffr