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Coord, Quality System
full-timeJapan

Summary

Location

Japan

Type

full-time

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About this role

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.

宮崎工場における品質システム業務の一部(製品リリース、文書管理、変更管理、NCR/CAPATSC品質運用、バリデーション管理、最終製品テスト、年次製品レビュー、内部/外部監査、マネジメントレビューなど)を実行します。

 品質オペレーショングループ連携した校正管理、文書管理をサポートします。

  • 手順とコンプライアンス要件に従って、彼女が担当するタスクを正確に実行します。

  • テストまたはドキュメントの記録を確認し、適切に維持します。

  • 機器や試験機器を正しく操作し、データを作成します。

  • タスクレポートのデータを入力および編集します。

  • EMSおよび改善活動を実施します。

Execute some of the Quality System tasks in Miyazaki Plant (Product release, Document control, Change control, NCR/CAPA, TSC quality operation, Validation control, Final product test, Annual product review, Internal/external audit, Management review, and others).

Support Calibration control, Document management in cooperation with the Quality Operation Group.

  • Execute accurately the tasks of which she takes charge, following the procedures and compliance requirements.

  • Review test or document records, and maintain appropriately.

  • Operate the equipment and test instruments correctly, and create data.

  • Input and edit data for task reports.

  • Conduct EMS and Kaizen activities.

<資格・学歴・経験>

  • 医療製品の製造と品質システムに関する基本的な知識 - GMP QMS、製品、製造プロセス、および試験機器。

  • コンピュータースキル(ExcelWordなど)

Qualifications / Education / Experiences

  • Basic knowledge about medical product manufacturing and quality systems - GMP, QMS, Products, Manufacturing process and Test instruments.

  • Computer skill (Excel, Word, and others)

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.

Other facts

Tech stack
Quality Systems,Document Management,Change Control,NCR,CAPA,Validation Control,Final Product Testing,Internal Audits,External Audits,GMP,QMS,Manufacturing Processes,Test Instruments,Computer Skills,Data Entry,Kaizen Activities

About Vantive

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.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Medical Equipment Manufacturing

What you'll do

  • Execute various Quality System tasks at the Miyazaki Plant, including product release and document control. Support calibration control and document management in cooperation with the Quality Operation Group.

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Frequently Asked Questions

What does a Coord, Quality System do at Vantive?

As a Coord, Quality System at Vantive, you will: execute various Quality System tasks at the Miyazaki Plant, including product release and document control. Support calibration control and document management in cooperation with the Quality Operation Group..

Why join Vantive as a Coord, Quality System?

Vantive is a leading Medical Equipment Manufacturing company.

Is the Coord, Quality System position at Vantive remote?

The Coord, Quality System position at Vantive is based in Japan, Japan. Contact the company through Clera for specific work arrangement details.

How do I apply for the Coord, Quality System position at Vantive?

You can apply for the Coord, Quality System position at Vantive directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Vantive on their website.