




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. **Your role at Vantive** Carry out the implementation of cost-saving projects, plant maintenance, new products/equipment/processes/materials and/or design modifications arising from manufactured products within the company; ensuring compliance with applicable regulations and customer requirements at each stage. **What you will do:** * Implement labeling for products manufactured by the company through approval of designs, artwork, and subsequently printed materials that comply with local, foreign, and/or corporate regulations. * Apply national procedures, standards, and regulations when implementing alternative processes or product alternatives. * Ensure proper transfer and subsequent implementation within the company of products manufactured by another subsidiary and/or contract-manufactured products. * Coordinate with Planning and Manufacturing departments the implementation of input changes (inventory depletion). * Update procedures and/or documentation applicable to the implementation of new products or updates to existing ones. * Draft, execute, and follow up on protocols involved in the implementation of a new project. **What you will bring:** * Bachelor's degree or Engineering in Pharmacy, Biochemistry, Chemistry, Biology, or Biotechnology. * 1 to 2 months of experience in Projects, Product Development, Manufacturing, or Quality (desirable). * Knowledge of Local Health Regulations (COFEPRIS) and international standards ISO 9001 / ISO 13485. * Proficiency in software applications (e.g., Office). * Advanced English (interview will be conducted in English). **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.


