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.
This role is aligned within Kidney care Solutions and the Containers Team working with the Sr. Manager, Solutions and Containers team in the USA. As part of the Product Sustenance team you will play a key role in defining, organizing, planning and leading global multi-functional projects related to all the modalities of Kidney care (PD, HD and Acute).
What you will be doing:
- Take charge of defining, prioritizing, planning, and leading the projects that are technically complex and multi-functional in nature
- Co-ordinate with multi-functional project team for effective collaboration and deliverables
- Work with Materials, Polymers, Plastics Processing (Extrusion/Molding), Mold flow studies
- Gain knowledge of structure property relationships of polymers/materials
- Exposure to material characterization tools, extractables and leachables and REACH complaint materials for drug products/medical devices
- Work with regulatory standards and quality management systems in the field of medical devices and related areas
- Strong Project Leadership and ability to flex as the role demands while interacting with internal and external stakeholders
- Establish, maintain and update technical & Design documentation according to Good Documentation Practices
- Active participation in the audits as the role demands
- Work with international/regional/national regulations and standards for drugs and medical devices
What you will bring:
- Bachelor's in Pharmaceutics, Material Science, Polymer Chemistry, Polymer Engineering, Chemical Engineering, Biology, Biosciences and Biomedical engineering
- Understanding of Design Control documentation
- Experience with Statistics and Six Sigma tools
Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $ 72,000 - 95,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.
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Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
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