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.
#J-18808-LjbffrSenior Regulatory Affairs Lead, Software Med Devices in alameda at Unknown Company
This position is listed as full time and onsite.