Description
Requirements:* Six Sigma Green/Black belt recommended.
* Minimum of five years experience in a related regulated medical device environment.
Essential Duties and Responsibilities:
* Manages the site CAPA program, working with Operations and Engineering to ensure timely issue resolution and CAPA closure.
* Manages the site Internal Audit program, working with Operations and Engineering to ensure timely issue resolution and Internal Audit closure.
* Will coordinate and prepare the site Management Review, ensuring that any action items are addressed.
* Designs and develops forms and instructions for recording, evaluating, and reporting quality data and monthly metrics.
* Analyze Quality data for management reporting, and advise management on potential improvements or enhancements to the quality system and processes in the company.
Please be in contact as soon as possible for this urgent position.
To find out more about Real please visit www.realstaffing.com