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Aidoc is looking for extraordinary people to join our industry-leading team that’s building cutting-edge artificial intelligence to reshape the future of healthcare. Named one of TIME magazine’s “50 Genius companies”, an innovative and exciting work environment, talented teams and a great work culture are just a few of the reasons why you’ll love working here.
Aidoc is recruiting a Post Market Surveillance and QMS Specialist in Tel Aviv. Join our team!
Aidoc is revolutionizing clinical decision-making with real-time clinical AI imaging solutions, impacting over 60 million patients annually. Our technology empowers physicians to diagnose urgent cases, ultimately improving patient outcomes.
Powered by our proprietary aiOS, Aidoc assists clinicians by precisely highlighting suspected pathological findings directly on medical images and prioritizing cases. This ensures that urgent patients receive the immediate attention they need.
As a leader in clinical AI, Aidoc has the most FDA-cleared Computer-Aided Detection (CAD) solutions, with adoption in more than 1,600 medical centers worldwide.
Since our founding in 2016, Aidoc has secured over $370 million in funding and was recognized as one of TIME’s 50 most genius companies.
The Compliance team at Aidoc is responsible for regulation, quality assurance, privacy, and security.
As a Post-Market Surveillance and QMS Specialist, you will lead post-market surveillance activities, including collaborating with stakeholders across Aidoc and preparing periodic reports as required by regulations. As a QMS specialist, you will serve as a key link between regulatory requirements and internal teams across the company. Your mission will be to ensure that Aidoc’s quality management system (QMS), regulatory submissions, and product compliance meet the highest industry standards.
In this role, you will act as a subject matter expert in post-market surveillance, including leading complaint investigations, reporting to regulatory authorities, and preparing required surveillance reports. You will also provide expertise in medical device quality requirements and lead critical activities that support our fast-growing business strategy.