Aidoc is recruiting a Director of QA & RA in Tel Aviv. Join our team!
Aidoc is a pioneering force in clinical AI. Our clinical AI imaging solutions help physicians quickly identify and diagnose urgent cases and improve patient outcomes. Built on Aidoc’s exclusive aiOS, we analyze and aggregate medical data to enable care teams to operationalize the unexpected and work seamlessly with a continued focus on the patient. Aidoc AI is always on, running in the background to change the foreground.
We have 17 FDA clearances, and our solutions are used in more than 1,000 hospitals, including leading health systems in the US. Funded by some of the industry’s leading VC’s, Aidoc has raised more than $250 million to date, and was chosen as one of TIME’s 50 most genius companies.
The RA team in AIdoc is unique in the extensive scope of medical devices it manages, and its pioneering position in the realm of AI regulation.
The team is responsible for receiving FDA, CE and other regulatory marking authorizations, ensuring conformity with all required medical device regulations and standards, maintaining Aidoc’s QMS, and assuring compliance with privacy requirements.
The Director of QA & RA is a pivotal link between the medical device regulators requirements to all company departments, promising Aidoc’s quality management system, regulatory submissions, clinical work, product verification and validation processes meet the highest regulatory standards.