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Regulatory Affairs Specialist

Cypress HCM
Irvine, CA Full Time
POSTED ON 5/24/2024 CLOSED ON 5/31/2024

What are the responsibilities and job description for the Regulatory Affairs Specialist position at Cypress HCM?

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  • 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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