Production Specialist (Temporary Contract)
Pubblicato il 30-09-2026 - Vantive in Grosotto
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
Join our Valtellina Plant and help drive operational excellence and processes in a highly regulated production environment. In this role, you will work closely with Production Supervisors and cross-functional teams to improve processes, enhance efficiency,
and support the manufacturing of products that make a meaningful difference in patients' lives worldwide.
Responsibilities
- Partner with Production Supervisors to identify, prioritize, and implement improvement initiatives emerging from Value Stream Mapping activities.
- Support continuous improvement projects focused on reducing waste, minimizing rework, and increasing operational efficiency.
- Support production departments in managing EBR events
- Review batch records to ensure accuracy, compliance, and product quality.
- Manage training activities for the departments, ensuring employees are appropriately trained and qualified
- Perform procedural updates and continuous improvement of production procedures and work instructions.
- Contribute to maintaining a culture of quality, compliance, and continuous improvement throughout the manufacturing organization.
Requirements
- Bachelor's degree in Engineering (Biomedical, Mechanical...) or Life Sciences (Chemistry, CTF, Biology...)
- Strong interest in manufacturing processes and continuous improvement methodologies.
- Excellent communication and teamwork skills.
- Good problem-solving and analytical capabilities.
- Good English knowledge, written and spoken.
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