Job Description

Regulatory Affairs Specialists

Work Location - 100 % Remote

Qualifications

• Working towards a Bachelors or Masters degree in regulatory affairs
• Entry-level knowledge of US and EU medical device regulations, 21 CFR 820 Quality System Regulation, and standards
• Proficient in using Microsoft Word, Excel, and PowerPoint
• Strong communication skills
• Results-oriented focus

Responsibilities

• Under direct supervision and guidance, an opportunity to be exposed to complex regulatory affairs strategies for medical device field
• Use 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/sales

Should 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.Recruiter

Supriya

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