Regulation Affair Director
Nadav Reuben is a senior executive and top management leader with over 22 years of experience in the medical device, biotechnology, and pharmaceutical industries, specializing in global Regulatory Affairs, Quality Assurance, clinical strategy, and operational leadership.
Throughout his career, Nadav has held multiple Vice President-level positions, serving as a key member of executive leadership teams responsible for driving company growth, operational scale-up, and global compliance.
He has led regulatory strategies and quality systems supporting FDA submissions, CE certification under EU MDR, MDSAP , MoH requirements, and global frameworks, while successfully managing complex international audits and inspections.
Nadav on his previous role, serves as VP QA & RA at Noga Medical Products, acting as a strategic partner to executive management and leading global regulatory and quality activities aligned with business expansion objectives. Previously, he served as VP Operations, Regulation, Quality & Clinical at Venus Concept, where he led company-wide regulatory and clinical strategy and established a new U.S. manufacturing site from planning through operational scale-up. Prior to that, Nadav was Senior Director and Head of Sites at Teva Pharmaceuticals, leading quality and regulatory operations across medical device and oncology divisions. He also held VP leadership roles at Biological Industries and CollPlant, supporting international growth, infrastructure development, and regulatory-driven market entry.
Nadav holds an MBA in Business Administration and a B.Sc. in Biotechnology, and is certified as CQA and CQM by the American Society for Quality (ASQ).
He is recognized for strategic thinking, strong execution, and a leadership style based on integrity, accountability, and cross-functional collaboration delivering measurable impact in regulated global organizations
