Senior Regulatory Affairs Lead, Software Med Devices
Listed on 2026-10-15
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Pharmaceutical
Healthcare Compliance, Regulatory Compliance Specialist
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.
Our organisation is growing, and we are hiring a Senior Regulatory Affairs Lead, Software Med Devices in Alameda, CA, United States.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Alameda, CA, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 90..
We aim to respond to suitable candidates as soon as possible.
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