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.

EDUCATION AND REQUIREMENTS:

• You will have a degree in Science/ Engineering or equivalent
• Process validation experience is desirable
• Knowledge of EU GMP and FDA regulatory requirements
• You will have critical thinking and problem-solving skills
• Ability to demonstrate solid decision making and problem-solving abilities.
• Membership of a professional body desirable

• Author validation protocols, reports and risk assessments
• Review engineering trials and product development documentation
• Complete Trackwise 8 validation and risk assessments
• Technical approval of validation documentation
• Lead projects to ensure they are executed in a controlled and compliant manner
• Provide status updates on projects
• Presentations and project management