Regulatory Affairs Specialist

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Precision’s goal is to provide breakthrough treatments for the one billion patients worldwide suffering from neurological illnesses. We are building the only brain–computer interface that is designed to be minimally invasive, safely removable, and capable of processing large amounts of data. To learn more about how Precision is connecting human intelligence and artificial intelligence, visit

Developing neural interfaces is an interdisciplinary challenge. Working at Precision means collaborating closely with some of the world’s leading experts in fields ranging from brain surgery to software and mechanical engineering to circuit design to microfabrication.
We are seeking a Regulatory Affairs Specialist to write and facilitate regulatory submissions and other technical papers related to our medical device brain-computer interface.

This is an extraordinary opportunity to join our core team to help shape the future of our company. Your work will help our product advance rapidly toward commercialization, so that we improve the lives of patients who live with neurological disorders.


  • Write about our complex brain computer interface (BCI) medical device which includes hardware and software components.
  • Interface across all business functions including hardware, software and product management teams to ensure a deep understanding of our device and development timelines.
  • With the help of our highly accomplished technical team and external regulatory consultants, write and facilitate regulatory submissions including clinical trial applications, IRB and IDE submissions, pre-submission inquiries, 510(k) and PMA applications.
  • Monitor newly published FDA guidelines and international guidance documents.
  • Collaborate with the rest of our team on technical manuscripts and academic whitepapers.


  • Expert at communicating complex technical ideas clearly and effectively.
  • Previous experience writing substantial contributions for (or leading entirely) at least one 510(k) application.
  • 2+ years’ expertise writing regulatory documentation for medical devices(comprising hardware or software), such as 510(k) applications, IRB and IDE submissions, PMA applications and clinical trial applications.
  • Has a science background either through education or work experience.
  • A self-starter who enjoys working to challenging deadlines.
  • A great collaborator who enjoys working as part of a high-performing, friendly, close-knit team.

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