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Edwards Lifesciences
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Irvine, California
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Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical ... journey.
As the Clinical Device Management Associate Analyst, you will develop and support
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AbbVie
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Irvine, California
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and in areas requiring select agents and Toxins access (i.e. Biosafety level 2 and biosafety level 3 ... lab investigations, CAPA, Change Control
• Experience working in a GMP regulated environment
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Parker Hannifin Corporation
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Irvine, California
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value is gained from each change, challenging as appropriate.
Monitors the wider Master ... appropriate Data driven regulatory requirements (i.e. DFARs, Data Privacy and GDPR
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