40 year expertise in the pharma industry, sure to be able to guide =, hands on, your business towards compliance with GxP regulations

2015- 2017Business Owner of Teva new LMS system. In charge of implementation of a new LMS in Teva sites across the world.

In charge of all auditing activities of Teva- third party manufacturers. In charge of planning, scheduling, performing and review of audit reports, training and certification of auditors around the globe.

Consultant for pharma companies:Hands –on: writing and review of documents, protocols, reports, SOPs; Educating & training, mentoring of employeesConsulting on General cGMP, product development, compliance, quality assurance and quality control issues with Israeli manufacturers, including ophthalmic aseptic production facility (Dr. Fisher), Radiopharmaceutical manufacturer (Isorad, as QP/Authorized pharmacist), API production, consulting on the process of generic products development and more.R&D consulting in Turkey (Abdi Ibrahim Ilac), Good Distribution practices consulting with Clalit health services.

In charge of taking a product all the way from R&D to maturity, i.e. market. Including : scale up, validation, clinical supplies, clinical studies, RA, and more.