Senior Regulatory Affairs Lead: Global Submissions
Listed on 2026-10-18
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Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
Cordis, in partnership with Selution, seeks an experienced Senior Regulatory Affairs Specialist in Irvine, CA. You will lead and author regulatory submissions, coordinate with engineering, QA, clinical teams, and regulators to ensure compliance with FDA, EU MDR, and other global requirements.
Responsibilities include PMA/IDE submissions, CE marking, and development of regulatory strategies for new and existing products.
We are looking to fill the Senior Regulatory Affairs Lead:
Global Submissions position at Cordis in Irvine, CA, United States.
All applications are reviewed carefully by our team.
The position is based in Irvine, CA, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 89..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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