My job contains many kind of applications of regulatory, quality assurance, pharmacovigilance,purchasing, import-export, planning &coordinating. Starting from the registration to the shipment of the products, for different countries, there are many well-organized projects. I am playing an influential role
in the processes of providing all needs for regulation (the application documents, working standards,impurities, reference standards, samples, packaging designs etc.); quality (the analysis certificates,changes of designs, SOPs, complaints); PSUR requests; purchasing (all needs for production factory; active
ingredients, raw materials, excipient, laboratory needs; chemicals, analysis devices etc.). Some of the demands are taken through imports and all the country demands are sent via exports. My role at import&export is only SAP processes and request the demands from related departments. Every country is a
project for us, so I am working as a Project Specialist for the countries I am responsible for.
●Provide guidance with interpretation/ translation policies and procedures to student.
● Support students with technical issues and perform administrative duties via phone, email and zoom.
● Work cooperatively with Program Coordinator, classified faculty and staff with special projects, scheduling students, monitoring student’s enrolment, using the SARS and MySite database.
● Assist with administrative work including answering phone calls,scheduling, rescheduling and cancelling appointments,filing documents.
●Responsible for providing excellent customer service and ensuring a positive customer experience.
• Analyzing the orders, received from customers, in accordance with their forecast figures and modifying them if needed.
• Generating orders in SAP system, preparing shipment documents and following up all procedures until its arrival.
• Following and evaluating the local stocks according to the sales and forecast figures.
• Managing forecast reports by analyzing customer stocks with respect to their sales figures.
• Corresponding customer requests and questions as soon as possible.
• Organizing and attending to customer visits.
• Coordinating all related departments in order to initiate the complaint process, and monitoring complaint procedure.
• Managing and following production plans in accordance with countries’ budgets and forecasts.
• Conducting medicine registration processes.
• Determining the products, which will be registered in the foreign countries, together with customers.
• Obtaining and presenting the necessary information from head office to customers in order to determine the new products.
• Attending the GMP audits of foreign authorities, and making coordination to compose the audit program and documents.
• Sustaining packaging design arrangements of needed products.
• Maintaining all design works and supplying packaging materials of future launch products in order to launch within the specified period.
• Sustaining designs works of existing products within the specified period when variations approved.
• Managing packaging materials’ usage in order to maintain the right materials for the production.