Description
DUTIES AND RESPONSIBILITIES:- Participate in data migration project to support Agile implementation
- Locate and verify engineering drawings
- Create bills of materials
- Locate and review FDA registration and 510(k) information
QUALIFICATIONS (Minimum Experience, Education, Computer Skills, etc.):
- A minimum of 4 years of experience in the medical device domain in either Quality Assurance or Regulatory Affairs.
- Experience in Quality Engineering or Regulatory Affairs
- Experience with MS Office required
- Experience with UniPoint, Agile PLM, or other quality system application desirable
- Experience with Oracle desirable
- Experience with, or certification from, ISO 13485
To find out more about Real please visit www.realstaffing.com