Diality, Inc. is seeking a Principal Regulatory Affairs Specialist to lead regulatory submissions for the Moda-flx Hemodialysis System and provide cross-functional regulatory guidance. You will manage 510(k)s, IDEs, and international submissions while ensuring compliance across development and post-market activities. The ideal candidate has extensive experience translating complex technical data into regulatory documentation, excels in fast-paced startup settings, and can drive projects to

Also on the board Same function, level within a rung

Level

Manager

Location

Irvine, CA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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