
10,000+ employees
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams globally. For 70 years, our team has driven meaningful innovations in kidney care. Today, Vantive’s people, solutions and services deliver over 1 million touchpoints each day to patients around the world. As we build on our legacy, we are focused on elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Our goal is to provide therapies that fit more easily into providers’ practices and patients’ lives. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.
🕒 February 16
🗣️🇪🇸 Spanish Required
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10,000+ employees
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams globally. For 70 years, our team has driven meaningful innovations in kidney care. Today, Vantive’s people, solutions and services deliver over 1 million touchpoints each day to patients around the world. As we build on our legacy, we are focused on elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Our goal is to provide therapies that fit more easily into providers’ practices and patients’ lives. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.
• Contribute and drive the Global CMMS and Calibration area for the Full Clone and Clean Project in Vantive. • Successfully project managed multiple Global CMMS and Calibration site implementation projects based on timeline, scope, and budget. • Ensure the development and management of all project planning, schedule and budget in conjunction with the Global CMMS and Calibration Program Manager. • Responsible for project tracking, status reporting, Identifying risks, and new requirements. • Support the creation/review of validation materials and the execution of validation activities. • Consistently provides clear and effective communication with all project stakeholders and Team. • Managing / Coordinating, the Global CMMS and Calibration team • Supervising User Access Management for Maximo license Users once cloned • Analyze business requirement/process, Identify, and understand broader business impact, assess alternative solutions, and propose preferred solutions • Collaborate with Infra team and all IT partners for activities related to the Global CMMS and Calibration Domain. • Work in conjunction with Quality and Compliance team to ensure corporate requirements, documentation, and application policy are up to date and approved. • Consult with CAB stakeholders to deliver applications and business improvements. • Co-ordinate application enhancements, system upgrades, database upgrades, operating system upgrades once cloned • Support external contractors to ensure a healthy, stable Maximo Environment.
• Bachelor’s degree in information technology, Computer Science, or a related field. • Minimum 5 years of experience working with CMMS and calibration systems; Maximo experience strongly preferred • 6+ years of experience in manufacturing environment. • Strong functional expertise in CMMS and spare parts and calibration. • Experience of System validation in a pharmaceutical environment, desirable • Spanish and English speaking and written communication skills are mandatory.
• Reasonable accommodation for individuals with disabilities globally
Apply Now🕒 February 9
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