Description
QA Analyst IIIKey responsibilities include:
DUTIES AND RESPONSIBILITIES:
* Participate in QMS software testing, and validation activities
* Create validation protocol and business requirements as it relates to QMS Tools
* Maintain QMS Software documentation
Requirements:
* A minimum of 4 years of experience in the medical device domain in either Quality Assurance or Regulatory Affairs.
* Experience in technical software documentation as it related to the medical device domain
* Experience with software validation in the medical device domain
* Experience with MS Office required
* Experience with a range of off the shelf software packages desirable
* Experience in working with all levels of the business.
Please apply ASAP to be considered. This is an excellent opportunity for anyone looking for a long term position with a family oriented medical device company and excellent people to work with!
To find out more about Real please visit www.realstaffing.com