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Regulatory Affairs SpecialistsWork Location - 100 % RemoteQualificationsWorking towards a Bachelors or Masters degree in regulatory affairsEntry-level knowledge of US and EU medical device regulations, 21 CFR 820 Quality System Regulation, and standardsProficient in using Microsoft Word, Excel, and PowerPointStrong communication skillsResults-oriented focusResponsibilitiesUnder direct supervision and guidance, an opportunity to be exposed to complex regulatory affairs strategies for medical device fieldUse regulatory research skills and entry level regulatory knowledge to support projects such as competitive regulatory assessments, initial regulatory strategy development and regulatory guidance for marketing/salesShould you be interested, please send me a copy of your resume in word format along with the following details ASAP. Name: Visa: Exp: Location: DOB: Rate: Thanks, Sr. RecruiterSupriya

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Level

Senior L5

Location

Denver, CO

Occupation

Regulatory Affairs Specialists

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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