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Shannon,
Ireland
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A Quality Engineer II applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimise product development
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Shannon,
Ireland
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A Quality Engineer II applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimise product development
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Cartago,
Costa Rica
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Make a meaningful difference to patients around the world. At Edwards Lifesciences facilities around
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Irvine, California
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a Systems Engineer II , this individual is responsible for evaluating system requirements and
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Irvine, California
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For over 50 years, the Critical Care business within Edwards Lifesciences (NYSE: EW) has operated at
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United States
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Imagine how your ideas and expertise can change a patient’s life. Our Global Supply Chain team plays
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Cartago,
Costa Rica
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Make a meaningful difference to patients around the world. At Edwards Lifesciences facilities around
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Irvine, California
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Make a meaningful difference to patients around the world. At Edwards Lifesciences facilities around
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Singapore
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Innovation starts from the heart. Edwards Lifesciences is the global leader of patient-focused innov
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Irvine, California
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Edwards Lifesciences has an opportunity for a Senior Engineer, Supplier Quality on the ... Engineer will apply knowledge of quality engineering principals and methods to ensure compliance with
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Irvine, California
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assigned.
What you’ll need (Required):
Bachelor’s degree in engineer or scientific with ... certifications.
Class II or Class III medical device industry.
Engineering methods (e.g., Six Sigma and
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Hybrid, California
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, Class II and/or Class III devices
• Full knowledge and understanding of EU and US requirements for
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Cartago,
Costa Rica
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Supervise employees and activities across areas of manufacturing for smooth and continuous operation
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Irvine, California
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, Class II and/or Class III devices
• Full knowledge and understanding of EU and US requirements for
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Dubai,
United Arab Emirates
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knowledge and understanding of global regulations relevant to medical devices (e.g., Class I, Class II and
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Irvine, California
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Class II and III medical device technologies and/or clinical studies background Required
**What
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Limerick,
Ireland
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Supervise employees and activities across areas of production for smooth and continuous operations.
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Salt Lake City, Utah
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levels exceeding the requirements of the Supervisor II
**What else we look for
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Nave 25,
Dominican Republic
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understanding of global regulations relevant to medical devices, Class II and/or Class III devices
• Solid
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Singapore
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Supervise employees across areas of manufacturing for smooth and continuous operations.
Key R
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Irvine, California
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Sciences field, with 5 Years experience Class II and III medical device technologies and/or clinical
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Irvine, California
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international regulatory compliances and frameworks such as ISO, SOX, BASEL II, EU DPD, HIPAA, and PCI DSS
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Singapore
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Supervise a team of employees in conducting technical training activities
Key Responsibilitie
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Irvine, California
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Full knowledge and understanding of global regulations relevant to medical devices, Class II and/or
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Irvine, California
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understanding of global regulations relevant to medical devices, Class II and/or Class III devices
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