- Initiate medical device quality assurance activities.
- Support device complaint investigation and failure analysis as required.
- Develop incoming inspection processes and document incoming inspection activities.
- Provide in-process QA support to include inspection and document review.
- Manage the sterilization process, including validations and product sterile loads.
- Track nonconforming material and lead Material Review Board (MRB) efforts
- 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
- Bachelor's degree
- Prior quality manufacturing experience
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Quality Engineer
2 weeks ago
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1 week ago
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Quality Engineer
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Quality Engineer
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Supplier Quality Engineer
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Supplier Quality Engineer
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Design Quality Engineer
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Senior Quality Engineer
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Senior Quality Engineer
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Manufacturing Quality Engineer
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Quality Engineer
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Supplier Quality Engineer
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Quality Engineer
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Senior Quality Engineer
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Quality Engineer
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Quality Engineer
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Quality Engineer
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