Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek ---- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.
Regulatory Affairs ensures compliance to medical device and IVD regulations globally. The Regulatory Affairs Department communicates with worldwide health authorities in the licensing of all products both in development or currently marketed globally. The Senior Regulatory Affairs Specialist will collaborate with Agilent international partners and subsidiaries to drive high profile regulatory submission projects. The person in this role will investigate complex global regulatory issues and will develop and execute strategic regulatory plans in countries outside of the US and EU. Job Responsibilities:
Yes, 10% of the Time
Carpinteria, CA, United States - 6392 Via Real
Special Skills Required:
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