Regulatory Affairs Specialist

3 weeks ago


New York, United States Cypress HCM Full time

· 0-2 years of experience in regulatory affairs, and/or experience in QA, R&D, Manufacturing or Project Management within the IVD industry · Working knowledge of FDA, and CE marking requirements for IVD products is a plus · Able to work independently and with others · Able to work with minimal supervision · Excellent computer applications skills · Strong customer orientation and focus

Salary: 90K



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