11 Aug
Quality Engineer
Vacancy expired!
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.
- Complete final acceptance activities.
- Manage the sterilization process, including validations and product sterile loads.
- Interface and take lead QA role in interactions with suppliers, contractors and consultants that supply components, subassemblies and contract processing.
- 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.
Provide in-process QA support to include inspection and document review.
Track nonconforming material and lead Material Review Board (MRB) efforts.
Lead complaint investigations on returned product.
Vacancy expired!