Principal Quality Engineer - Medical Device GMP/QSR Expert
-
Engineering
Quality Engineering, Biomedical Engineer, Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
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.
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- Medical Device GMP/QSR Expert role at Regulatory Jobs?
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This posting is for the Principal Quality Engineer
- Medical Device GMP/QSR Expert role at Regulatory Jobs, based in Grand Rapids, MI, United States.
We are looking to fill the Principal Quality Engineer
- Medical Device GMP/QSR Expert position at Regulatory Jobs in Grand Rapids, MI, United States.
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