Hello Everyone,
I am seeking a Sr. Manager of Regulatory Affairs (possibly Director) for my client located in the Atlanta Metro area. This is a rare opportunity to be a part of a groundbreaking IDE clinical trial followed by an original PMA and to round out your regulatory career with EU MDR submission work, Class I, IIa, IIb, and Class III and to bring a variety of device classifications to a global market and support product development of more.
They are looking for someone with 8+ years' experience in medical device regulatory submissions and IDE support. PMA experience is desirable but not required.
If you would like to learn more about this opportunity, please email me your resume at davidleo@biomedical-resource.com or call me 413.596.2883.
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Best...
David Leo
Chair - RAPS Boston Chapter
President - Biomedical Resource Consultants, Inc.
davidleo@biomedical-resource.com / +1 (413) 596-2883
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