Vantive: A New Company Built On Our Legacy

Baxter is on a journey to separate our ~$5B 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 separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.

The Renal Lead System Integrator (LSI) team is a part of the R&D organization that supports the Renal Care business unit. Within the team we provide project management activities in all product phases, innovation initiatives, new product development and improvement programs for existing therapy systems. This collaborative role gives you the direct opportunity to define solutions to new products and services to patients and continue Baxter’s mission to save and sustain lives.

Baxter is a global company with R&D sites at multiple locations in the world; competences and capabilities are spread over the different R&D sites, and you will commonly collaborate with colleagues across several of these R&D sites. Work assignments within the team are highly variable and we can promise you a work environment with exciting project management challenges and variability in your day-to-day activities.

Lead System Integrator co-ordinates/leads R&D team within a Project or Program with her/his Project Management and Technical Leadership skills.

Essential Duties and Responsibilities:

• Support research and development (R&D) project management work and research for medical devices and regulated healthcare products

• Owner of R&D program schedule creation, tracking, and execution. Responsible for delivering an integrated product with detailed plans from primary iteration to successful system verification completion

• Participates as a member of cross functional teams and/or integrates cross functional inputs into project delivery

• Supports project execution and proactive risk management.  Effectively tracks project status, risks and external spend

• Basic understanding of and adherence to FDA, ISO and IEC design control procedures, regulations, and standards

• Prepares project reports, analyses and delivers presentations to R&D leadership on a weekly basis

• Supports scheduled meetings in R&D, develops and manages agenda, creates minutes, and follows up action items throughout the integration steps

• Establish project communication channel. E.g., Teams group, Status meeting, Escalation matrix, etc. 

• Facilitate/organize project design reviews and change control meetings 

Qualifications:

• Experience in project management principles and methodologies

• Strong interpersonal and communication skills in written and verbal form

• Ability to provide technical leadership for medical device projects with medium complexity and scope

• Ability to decompose complex problems into actionable task lists

• Understanding of design requirements for development, validation, and verification of medical products

Education and Experience:

• Bachelors degree in Engineering or equivalent field

• 1+ years of R&D experience; experience in medical device industry preferred

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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