
Job description
Vantive is a vital organ therapy company seeking a QA Manager to lead quality assurance efforts for medical devices and pharmaceuticals. The role involves ensuring compliance with laws and regulations, improving/maintaining product quality, and realizing the "Quality Policy." The QA Manager will be responsible for managing product quality tasks, including quality agreements with domestic and overseas manufacturers, and performing GMP management work.
The QA Manager will be responsible for various tasks, including document management, creating and revising product master formulas, managing QMS-related records, supporting annual product reviews, and executing or supervising other quality assurance work.
This role requires a strong understanding of GQP and QMS regulations, as well as experience in quality assurance management. The ideal candidate will be able to lead a team, manage tasks efficiently, and communicate effectively with stakeholders.
Company
Keep exploring
Sign in to see similar jobs
Create a free account to discover roles related to this posting.

Healthcare • Manufacturing
Vantive is a leading vital‑organ therapy company specializing in kidney care and dialysis solutions. With 70 years of experience, the company provides a comprehensive portfolio of digital platforms, advanced services, and therapeutic products that support over one million patient interactions daily worldwide. Vantive’s offerings are designed to integrate seamlessly into healthcare providers’ workflows, enhancing flexibility and efficiency for care teams while improving the quality of life for patients. Building on its legacy, Vantive is expanding beyond dialysis to develop innovative therapies for other vital organs, aiming to deliver treatments that are easier to administer and more adaptable to patients’ needs. The company’s focus on digital innovation and service excellence positions it as a forward‑thinking employer for professionals dedicated to advancing healthcare outcomes.