Validations and change controls referent.Approval of protocols, procedures and reports.Accompanying and approving validations for various equipment, piping and faucets, clean rooms, warehouses, computerized systems, shipments.Accompanying and approving changes in the plant, accompanying calibration deviations and deviations in water sampling and pure steam.

Systems and machines validation engineer at Teva Jerusalem plant.Performs validations for equipment and machinery on production lines.Writing protocols, procedures and reports. Conducting risk management and investigations.Performing temperature and humidity mappings in clean rooms and warehouses.Responsible for validation in the project to implement "serialization" of all products in the factory as part of the company's global project.

Validation engineer at "Omrix" in project for the establishment of a new biopharmaceutical plant under GMP conditions.A computerized system validation (CSV), air conditioning (HVAC) validation and general facility validation.Drafting procedures, forms of work, protocols and reports (SOP, RA, IQ, OQ, VSR).Execution of qualification protocols (IQ / OQ) and review of commissioning protocols (IC / OC).Also, responsible for coordinating tasks (Change Control / Request) and discrepancies reports in the project.Responsible for commissioning new equipment, confirmation of receipt of the equipment and its installation (RV / IV), and update relevant drawings.

Billing referent in Operations DepartmentReceiving data, distribution and sorting, and placing them into a computerized system. Exceptional production and maintenance reports.Ability to make decisions and handle with data exceptions.Training new employees, monitoring and supervision of their work integrity.