Senior Regulatory Affairs Specialist

Chicago  ‐ Onsite
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Keywords

Description

My Client is currently looking for a Senior Regulatory Affairs Specialist in Chicagoland area. They are looking for someone who has a strong medical device background. This is an expanding company that is looking for someone that can grow with them and move up in the company. They offer great benefits, bonuses and vacation.

If you are interested or know of anyone that would be a good fit for this role please email me your resume.

Essential Skills:

-Bachelors Degree (prefer in Science)

-3-7 years regulatory affairs experience

-3 years medical device background

-510k experience a must (submission with your name on it preferred)

-Expert knowledge of medical device regulations, standards, current industry practices and strong experience with interpretation and application

-Experience with hardware and software of medical devices

-Software submissions experience

-Proficient in Microsoft Outlook, Microsoft Work and Microsoft Excel

Desirable Skills:

-Familiar with international regulations (U.S./Canada)

-PMA experience (authoring it preferred)

To find out more about Real please visit www.realstaffing.com
Start date
01/2014
From
Real Staffing
Published at
17.12.2013
Project ID:
641673
Contract type
Permanent
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