Senior Regulatory Affairs Lead, Software Med Devices
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Pharmaceutical
Job Description & How to Apply Below
Abbott Laboratories seeks a Senior Regulatory Affairs Specialist for Lingo in Alameda, CA. You will support regulatory activities for Class II software medical devices, collaborating with product teams to ensure compliant submissions and labeling throughout development and post‑market stages.
The role emphasizes cross-functional leadership, regulatory strategy, and robust documentation to meet timelines and FDA requirements.
We are currently recruiting a Senior Regulatory Affairs Lead, Software Med Devices for our team in Alameda, CA, United States.
We have an opening for a Senior Regulatory Affairs Lead, Software Med Devices in Alameda, CA, United States within Legal, Management & Operations.
This role, Senior Regulatory Affairs Lead, Software Med Devices at Thornton Tomasetti, could be your next opportunity.
Are you ready to take on the Senior Regulatory Affairs Lead, Software Med Devices role at Thornton Tomasetti?
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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