Regulatory Affairs Specialist

4 weeks ago


Irvine, 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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