
Hemispheric builds AI systems that interpret brain activity to enable research and practical neurotechnology applications. The company develops foundational AI models and algorithms for decoding neural signals, using machine learning and deep learning techniques to translate brain data into usable outputs. Its products and tooling are aimed at neuroscience researchers and organizations building neurotech devices and applications. Hemispheric operates in the foundational AI for neuroscience category and focuses on model development and research partnerships to support downstream neurotechnology use cases.

Hemispheric builds AI systems that interpret brain activity to enable research and practical neurotechnology applications. The company develops foundational AI models and algorithms for decoding neural signals, using machine learning and deep learning techniques to translate brain data into usable outputs. Its products and tooling are aimed at neuroscience researchers and organizations building neurotech devices and applications. Hemispheric operates in the foundational AI for neuroscience category and focuses on model development and research partnerships to support downstream neurotechnology use cases.
We are seeking an to lead and manage all regulatory interactions, including FDA documentation, submissions, and communication. This position plays a critical role in ensuring compliance and regulatory readiness for our AI-based neurotechnology products. The ideal candidate brings medical regulatory expertise—someone who understands the nuances of QMS systems, SW/AI-as-a-medical-device, and non-invasive medical device regulation.
In this position you will:
Our ideal candidate will have:
This is a full-time position, located in Tel-Aviv. If this sounds exciting, get in touch: joinus@hemispheric.ai
At HEMISPHERIC, we care about people and do not discriminate based on... anything.