I bring deep, multidimensional experience at the heart of the medical device industry, combining excellence in quality, sharp systemic understanding, and strong familiarity with international regulatory methodologies. My academic background includes a B.Sc. in Life Sciences (Bar-Ilan University), an M.Sc. in Medical Sciences (Faculty of Medicine, Tel Aviv University), and an M.A. in Law (Bar-Ilan University).

I am certified as a Lead Auditor for ISO 13485 by the Standards Institution of Israel, with additional accreditation covering the FDA’s Quality System Regulations (21 CFR Part 820) — placing me in a unique position to help companies integrate top-tier quality readiness with business excellence.

My professional background reflects deep, hands-on engagement at the core of the medical device industry, especially within companies pioneering integrated hardware and software solutions. I have led the creation of critical quality documentation, held a pivotal role in sophisticated software validation projects, proactively surfaced early-stage quality risks, and collaborated with multidisciplinary teams — bringing a proactive quality perspective that amplified operational impact and supported stronger business outcomes.

What distinguishes my work is the ability to go beyond compliance — to anticipate, simplify, and connect quality to real growth and value. I offer executive teams a quiet yet sharp perspective that uncovers hidden weaknesses and restores quality to its rightful place as a strategic and business driver.