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Confirmed on the employer's own hiring board on Nov 7, 2026. First seen by Alion on Nov 6, 2026.

Overview
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Vantive is a vital organ therapy company headquartered in Deerfield, Illinois, United States, that develops and supplies kidney care products such as peritoneal dialysis and hemodialysis systems, acute organ support therapies, digital solutions and related services. Formerly the kidney care business of Baxter, it builds on about 70 years of work in dialysis and operates worldwide, with sites in Bengaluru, Mexico, Poland, Ireland, Minnesota and Australia. It hires research and quality engineers, manufacturing and project engineers, dialysis sales managers, delivery drivers and warehouse staff, supply chain, ERP and IT specialists, and finance, audit and tax professionals.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients- that is what Vantive aspires to deliver.

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 is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

Summary:

This position is responsible for the development, validation, and transfer of analytical methods, as well as support to analytical testing. The successful candidate will possess solid “hands-on” technical abilities, excitement, a passion for their work and the impact it has on meeting the needs of patients.

  • Effectively contribute basic technical knowledge and skills to a variety of projects within relevant discipline
  • Interact effectively with a variety of disciplines. ·
  • Conduct routine research and design experiments with some assistance.

Essential Duties and Responsibilities:

Hands-on experience with analytical instruments such as HPLC, UPLC, GC, IC, UV, Potentiometer and other general techniques along with its data interpretation.

· Execute analytical method development, validation, transfer of methods for new product development and sustaining product projects. Provide some analysis/re-design of key experimental procedures. Independently select techniques and procedures to solve problems within area of responsibility.

· Execute routine analytical activities in accordance with global/local procedures within negotiated deadlines.

· Recommend appropriate designs, techniques, and processes for a specified sequence of tasks where needed including drafting analytical plan.

· Preparing analytical strategies/identify and review gaps in analytical methods, drafting method of analysis.

· Responsible for qualification and calibration of laboratory instruments/equipment's/procedures.

· Preparations of Validation/Transfer protocols, reports for execution of Class B studies.

· Demonstrate ability to apply technical theories and principles to projects within area of expertise for non-routine tasks. Analyze and determine best solutions to non-routine experimental design or research problems with minimal assistance. Accurately assess results for validity and conformance to specifications.

· Planning and execution of laboratory experiments associated with assigned projects.

· Support Laboratory investigation (OOS/OOT/Incidents/NCR)

· Good analytical and research skills.

· Maintain lab equipment and troubleshoot or report on malfunctions.

· Ensure compliance with laboratory health and safety guidelines.

· Good knowledge of laboratory health and safety standards.

Coordinate and ensure follow-up of technical activities in collaboration with key stakeholders, with respect of project commitment, quality procedures and business needs.

· Establish, maintain and update technical documentation according to Good Documentation Practices and follow all other laboratory compliance.

· Participate to multi-functional and international project team for effective collaboration and deliverables.

· Ensure good internal and cross-functional communication and regular status update of activities.

Reasonable Accommodation

Vantive 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. Form Link

Recruitment Fraud Notice

Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive 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.

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