Our staff combines fresh perspectives whith extensive experience to drive innovation in science and business models

Ofer has over 18 years of experience in the pharmaceutical, biotechnology, and medical device industries, specializing in compliance, quality assurance, validation, regulatory affairs, and cybersecurity. He holds a BSc in Biotechnology Engineering, an MSc in Environmental Engineering, and a PhD in Computer Science, along with certifications as an ISO Lead Auditor in ISO 9001:2015, ISO 13485:2016, and ISO 27001:2022. His expertise spans the pharmaceutical, biotechnology, medical device, and cosmetics sectors, with deep knowledge of quality assurance, validation, manufacturing processes, regulatory affairs, and the implementation of AI in systems. He has a proven track record in creating, implementing, and leading quality management systems, as well as providing training in these areas. His success includes leading inspections by the FDA, Health Canada, and other regulatory bodies, receiving an award for outstanding quality records, reducing regulatory penalties, and eliminating product launch errors. Known for his strategic vision, excellent management skills, and ability to prioritize tasks under tight deadlines, he has worked with major companies across North America, Europe, and Asia to improve processes, reduce costs, and establish interfaces between QA, R&D, regulatory affairs, and other departments.

As the Chief Operating Officer of the company, Noga brings a master's degree in clinical psychology and a strong skill set in managing daily operations. With a deep understanding of organizational behavior and interpersonal dynamics, she ensures seamless coordination across all departments, fostering collaboration and effective communication. Her expertise in overseeing operational workflows allows her to optimize resource allocation, manage client projects, and ensure the company consistently meets its goals and client expectations.

Known for her strategic thinking, she plays a key role in driving operational excellence, improving efficiency, and maintaining a positive, productive work environment.

With over 8 years of experience in the pharmaceutical and medical device industries, Charles has a strong focus on quality assurance, validation, research and development, and regulatory affairs. Holding a BSc in Biochemistry and a PhD in Cellular and Molecular Medicine, with a specialization in developmental signaling pathways, Charles has extensive management and consulting experience in global pharmaceutical, biologic, and medical device sectors. He has successfully led drug product development from conception through GMP manufacturing, managing multiple complex projects under accelerated timelines. Known for building and leading highly productive, multifunctional teams, he excels in adapting to new challenges and roles, with a strong collaborative approach to project development and management. His expertise includes team building, improving communication strategies, strategic planning, and exceptional problem-solving skills. With excellent oral and written communication abilities, he can synthesize complex scientific concepts and translate them into successful product and research program ideas.