Regulatory Affairs Associate
software technologyDenver, CO
Regulatory Affairs Associate
software technologyDenver, COSenior L5
Electromedical and Electrotherapeutic Apparatus ManufacturingSurgical and Medical Instrument ManufacturingSurgical Appliance and Supplies Manufacturing
APPLY NOW (opens in a new tab)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