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Philips
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Ontario, California
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Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team ... minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software
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Philips
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San Diego, California
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Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team ... minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software
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Philips
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Pittsburgh, Pennsylvania
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Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team ... minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software
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Philips
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Cambridge, Massachusetts
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Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team ... minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software
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Philips
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Orange, Ohio
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Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team ... .
You have a minimum of a Bachelor’s Degree in Regulatory Affairs, technical or science related field
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Philips
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Rosemont, Illinois
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Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team ... minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software
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Philips
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Plymouth, Minnesota
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Reporting to the Director of Regulatory Affairs, the Senior RA Specialist will collaborate with global team ... minimum of 7 years' Regulatory Affairs experience within FDA regulated, complex Medical Device/Software
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Stryker
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Bengaluru,
India
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Summary:As a Principal Medical Affairs Specialist, you will ensure successful preparation of high quality ... guidelines preferred.
Excellent knowledge of regulatory guidelines (FDA/CFR; EN540/ Med DEV/GCP/EU MDR
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Philips
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Plymouth, Minnesota
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Principal Regulatory Affairs Specialist, Software (U.S. Hub based)
Clinical Integration ... + years of experience in Regulatory Affairs in the medical device industry. SaMD experience and extensive
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Philips
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Colorado Springs, Colorado
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Principal Regulatory Affairs Specialist, Software (U.S. Hub based)
Clinical Integration ... + years of experience in Regulatory Affairs in the medical device industry. SaMD experience and extensive
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Philips
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Cambridge, Massachusetts
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Principal Regulatory Affairs Specialist, Software (U.S. Hub based)
Clinical Integration and ... compliance._
You're the right fit if:
You’ve acquired 7+ years of experience in Regulatory
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Philips
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Bothell, Washington
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Principal Regulatory Affairs Specialist, Software (U.S. Hub based)
Clinical Integration ... + years of experience in Regulatory Affairs in the medical device industry. SaMD experience and extensive
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Philips
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Orange, Ohio
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Principal Regulatory Affairs Specialist, Software (U.S. Hub based)
Clinical Integration ... + years of experience in Regulatory Affairs in the medical device industry. SaMD experience and extensive
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Philips
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Pittsburgh, Pennsylvania
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Principal Regulatory Affairs Specialist, Software (U.S. Hub based)
Clinical Integration ... + years of experience in Regulatory Affairs in the medical device industry. SaMD experience and extensive
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Philips
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San Diego, California
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Principal Regulatory Affairs Specialist, Software (U.S. Hub based)
Clinical Integration ... + years of experience in Regulatory Affairs in the medical device industry. SaMD experience and extensive
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