Engineer Quality

Profile

We are seeking an Engineer, Quality for a very important client.

The purpose of this position is to initiate medical device quality assurance activities. These activities must be in accordance with FDA Quality System Regulation, ISO13485 and other international standards. This position will also support device complaint investigation and failure analysis as required. Essential Duties and Responsibilities: Develop incoming inspection processes and document incoming inspection activities. Provide in-process QA support to include inspection and document review. Complete final acceptance activities. Manage the sterilization process, including validations and product sterile loads. Track nonconforming material and lead Material Review Board (MRB) efforts. Interface and take lead QA role in interactions with suppliers, contractors and consultants that supply components, subassemblies and contract processing. Lead complaint investigations on returned product. Manage corrective action and quality improvement activities. Manage aspects of internal quality system relating to receiving inspection, calibration, MRB, etc. Assist in the performance of quality system internal auditing. Support quarterly management review meetings. Establish, monitor and evaluate quality system metrics.
Requirement:
The ideal candidate will possess the following qualifications:
How to Apply:
If this position is a fit, simply click on the recruiter's email above, attach your resume, and hit send.

If this position isn't quite right, click here
to let us know what you are looking for and our recruiters will get to work finding something that is a better match.

Company info

Sign Up Now - HRCrossing.com