This inclusive employer is a member of myGwork – the largest global platform for the LGBTQ+ business community. Vantive: A New Company Built On Our Legacy Baxter is on a journey to spin off 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 Covering this role, you'll be accountable for activities related to complaints and nonconformities technical investigation, according to applicable procedures. I'll report to the Qa Ops Investigation Supervisor and you'll collaborate with a team that supports our mission: Save and Sustain Lives. What you'll be doing Performs activities related to investigation of customer complaints and manufacturing nonconformances in order to find the root causes of events, according to applicable procedures; Coordinates complex root cause analysis activities and provide support to the investigation team, ensuring that activities are conducted with appropriate scientific methods and following a DMAIC approach; Develops and implements experiments and tests to confirm or rule out potential root causes, demonstrating knowledge id Design Of Experiments (DOE) and statistical analysis; Writes investigations reports in order to properly document the activities in accordance with good documentation practices (GDP); Manages critical quality issues and keeps track of their resolution processes, interfacing with subject matter experts from different areas and, when required, leading the investigation teams; Supports his supervisor in order to identify the immediate, corrective and preventive actions as per continuous improvement process; Supports in case of audits; Escalates to the quality site management and to senior managers relevant and critical quality issues; What you'll bring Degree in Engineering (biomedical, electronical, mechanical …); 4-5 years of experience in Quality area in the medical industry or other fields; Knowledge of principles of dialysis/hemodialysis products; Previous experience in Project Management will be considered a plus; Organization skills and ability to do multiple tasks at once; Good communication and interpersonal skills; Problem Solving attitude; Fluent in English. #LI-CG1 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. Recruitment Fraud Notice Baxter 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 . 124784
