Senior Regulatory Affairs Lead: Global Submissions
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Pharmaceutical
Job Description & How to Apply Below
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.
Are you ready to take on the Senior Regulatory Affairs Lead:
Global Submissions role at Cordis?
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.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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