assistant supervisor

at  Vantive

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:

• Diploma or equivalent

EXPERIENCE:

• Diploma with 2 years experience. Fresh Graduates are welcomed to apply as training will be provided
• Language profociency: English
• Good communication, interpersonal and problem solving skills
• Computer literacy with ability to handle production data in system
• Experience in EMS, GMP and other regulatory requirements will be an advantage.
• Knowledge of lean manufacturing and six sigma will be an advantage
• 12-hour shift (day or night) is required.
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RESPONSIBILITIES:

Prepare, coordinate and monitor work schedule to achieve shift production target. Manage shift manpower deployment such as line balancing, leave management and overtime scheduling. Conduct daily shift briefing to line operators on production matters. Review shift labour efficiency and scrap data to drive improvement. Conduct training to line operators on process SOP update. Manage inventory on raw material, product WIP and daily scrap to ensure shift to shift inventory accuracy in system. Review work order accuracy, amend work order information, perform work order closure in all manufacturing systems. Troubleshoot and solve the manufacturing systems errors to minimize the impact to production. Drive Kaizen submission to meet the department target. Provide support for Safety, Quality and regulatory audits.