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.

Summary

This is a great opportunity to be responsible for defining global regulatory strategies and submissions in support of new and existing marketing authorizations in a global business unit with focus on electromechanical devices.

You'll lead functional team working on electromechanical devices.

What you'll be doing

Provide technical and strategic input for regulatory decisions aligned with business strategy  Identify and prioritize key areas of risk and probability of occurrence as well as ensure implementation of mitigation plans and follow ups  Monitor, evaluate, and interpret all applicable regulatory requirements, assure compliance with Baxter and external standards  Assess impact of new regulations and provide feedbackEvaluate technical and scientific information, identify deficiencies, implement and execute strategies to remediate risks  May act as primary contact for meetings with regulatory authorities including planning and leadership  Maintain appropriate communication within the RA function, with GBU Marketing, and with other functions primarily at the project team level  Plan and manage complex projects and prioritize workload  Initiate, manage and maintain operational activities in support of new and existing marketing authorizations  May manage regulatory budget at project level  May represent Baxter interests in industry and working groups  Set team, group, or service objectives to assure they align with the regulatory strategy  May provide direct supervision of individuals including mentoring, performance management and staffing decisions​ 

What you'll bring

Bachelor/Master's degree or country equivalent in a scientific discipline  (PhD will be an advantage)   +7 years experience in RA, including managing people or projectsExpert Regulatory knowledge in electromechanical devicesSound basis of Scientific (Training/ Communications) knowledge  Ability to oversee multiple projects in a matrix team environment  Ability to work effectively in multinational/multicultural environment  Interest in Regulatory Intelligence and experience managing standard compliance and regulation updatesExcellent oral and written communication and presentation skills  Excellent interpersonal and collaboration skills, including diplomacy to negotiate conflicting priorities  Ability to lead, coach, and motivate others  and to accomplish results through othersFluent English knowledge

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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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