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Your Search Term(s): Clinical » Regulatory Affairs » Medical
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Company Job Title Location Posting Date
Aerotek Clinical  Sr. Regulatory Affairs Specialist Minnetonka, Minnesota 9/9/2014
...regulations. Mainly responsible for assisting in planning and writing 510(k) and PMA submissions to the FDA. Must Haves: 5+ years experience in Regulatory Affairs Experience with 510(k) and PMA submissions Medical Device Experience

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