Job Description

Vantive: A New Company Built On Our LegacyBaxter 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\xe2\x80\x99t settle for the mediocre. Each of us are driven to help improve patients\xe2\x80\x99 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:Junior Research Associate within Renal Business, is responsible for technically leading projects/tasks/activities related product development and lifecycle management of peritoneal dialysis products.Essential Duties and Responsibilities:

• As Tech Lead or Change Owner, define, organize, plan, and execute activities related to product design change, supplier related changes, new product registration and strategic or value improvement projects in compliance with current international/regional/national regulations with support from senior colleagues as in when necessary.
• Propose, formulate, and coordinate action plan for implementation of changes and related activities by working closely with PDO Organization, Project Management, Regulatory, Quality, senior colleagues, and the other cross-functions.
• Expected to develop, document, test and manage product related changes in accordance with established Renal Care product processes and stay in alignment with Quality Management System.
• Ensure good internal and cross-functional communication and regular status update of activities.
• Establish, maintain, and update technical & Design documentation according to Good Documentation Practices.
• Propose, participate, or lead ideation sessions for product enhancement and exploratory activities to foster innovation culture within team.
• Assist in providing technical support to queries from MOH authorities or auditors (internal/external) in due time by collaborating with cross-functions and subject matter experts.
• Ensure Quality & Compliance to Baxter policy/Ethics/Data Integrity.

Qualifications:Masters in Science or Pharmaceutical disciplines is required.Education and/or Experience:\xc2\xb7 Masters degree in Science or Pharmaceutical disciplines is required.\xc2\xb7 Adequate orientation towards Renal PD therapies and products with time.\xc2\xb7 Adequate knowledge of product development stages and life cycle management required for effective collaboration with cross-functions and execution of project deliverables.\xc2\xb7 Adequate knowledge of Design Control documentation, Process, and Quality Management Systems.\xc2\xb7 Adequate knowledge of international/regional/national regulations and standards.\xc2\xb7 Demonstrate Project Management skills in due time.\xc2\xb7 Demonstrates flexibility and the ability to shift gears between projects comfortably.\xc2\xb7 Excellent oral and written communication skills.Reasonable 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 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 .

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