GQP Specialist, Medical Device

A leading multi-national medical device company that has been providing physicians and patients with quality products in Japan for over 20 years. The company has enjoyed stable growth over recent years and is aiming for the number 1 market share in Japan of it’s main product line.

Opportunity

You will report to the Group Manager of the GQP team and will be responsible for assisting the team with auditing manufacturing facilities both in Japan and overseas. You will also be required to periodically check and maintain GQP and other related documents.

Requirements

You will have:

* Over 2 years of medical device Quality Assurance/Quality Control or Regulatory Affairs experience.

* Experience of working with Class III/IV medical devices (preferred).

* GQP knowledge.

* Experience of handling quality assurance documents.

* Experience of manufacturing plant inspections.

* Business level Japanese.

* Conversational English.

Benefits

* Opportunity to join growing company.

* Extensive training and development program.

This position, GQP Specialist, Medical Device, was posted on January 23, 2010. Since this job has been published, it has been viewed 41 times.