Job description
Responsibilities:
- Provide in-process QA support to include inspection and document review.
- Complete final acceptance activities. Manage the sterilization process, including validations and
- 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.
- 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.
- product sterile loads.
- BS/MS degree in engineering or science.
- 3-5 years of related engineering experience.
- Quality engineering experience.
- Medical device or similar regulated background is plus.
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