QA Analyst

Carlsbad  ‐ Onsite
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Keywords

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
Start date
02/2014
Duration
6 months - Hire
From
Real Staffing
Published at
21.02.2014
Project ID:
668593
Contract type
Freelance
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