Previous Job
H - Quality Engineer 1 RECRUITED - 18M014 - 100030
Ref No.: 14-01683
Location: Newark, Delaware
Pay rate max $45/hr

Seeking a Quality Professional who has the following experience:
Project Management Experience
Chemistry Background
Medical Device Manufacturing Experience
FDA 21 CFR Part 820
ISO 13485
Warning Letter Remediation
CAPA Systems
Medical Device Reporting (MDRs)
Complaint Handling
Medical Device Design
Design History File (DHF)
Batch Records
4 Year Technical Degree Required - Bachelors
ASQ Certification a plus

Contractors will be doing look backs of various documents associated with medical device compliance.
They will be reviewing CAPA, DHFs, MDRs, Batch Records, Complaints, etc... for completeness and compliance.

7-10 years experience in quality with FDA Medical Devices