Principal Quality Engineer - Medical Device GMP/QSR Expert
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Engineering
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Quality Assurance - QA/QC
Job Description & How to Apply Below
Medtronic, Inc. in Grand Rapids, MI is seeking a Principal Quality Engineer to oversee quality for finished medical devices and to support manufacturing operations for regulatory compliance and product certification.
You will coordinate quality engineering activities, drive CAPA, risk management, and process improvements, and apply advanced statistical methods using Minitab and Power BI to ensure compliant, high-quality products.
Join us at Regulatory Toolkit as our next Principal Quality Engineer
- Medical Device GMP/QSR Expert in Grand Rapids, MI, United States.
Consider building your career as a Principal Quality Engineer
- Medical Device GMP/QSR Expert at Regulatory Toolkit.
The Principal Quality Engineer
- Medical Device GMP/QSR Expert position in the Engineering field is open for applications.
We have an opening for a Principal Quality Engineer
- Medical Device GMP/QSR Expert in Grand Rapids, MI, United States within Engineering.
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