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نُقدّر رأيكِ

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تم إلغاء حظر المستخدم بنجاح
جون مجدي, Head of Naming & Labeling Department

جون مجدي

Head of Naming & Labeling Department ·Central Administration for Pharmaceutical Affairs, MOH

مصر

بكالوريوس, pharmacy

الخبرة العملية

مجموع سنوات الخبرة: 17 سنوات, 0 أشهر

Head of Naming & Labeling Department

أغسطس 2015 - حتى الآن

Central Administration for Pharmaceutical Affairs, MOH

القاهرة، مصر

أغسطس 2015 - حتى الآن

• Revision & Selection of Trade Names for new drug applications.
• Revision of outer & inner labels of pharmaceutical drugs.

مجال الشركة:
صناعة الدواء
الدور الوظيفي:
إدارية

Deputy Director of Drug Shortage and Subsidized Drugs department

ديسمبر 2014 - يوليو 2015

Central Administration for Pharmaceutical Affairs, MOH

القاهرة، مصر

ديسمبر 2014 - يوليو 2015

• Community pharmacies (Local Market) follow up.
• Governmentally supplied drugs (MOH Tender) Follow up.
• Important pharmacological groups and drug categories (CVS, CNS, Biological products, Life-saving drugs, etc.) follow up by monthly monitoring distributors' stocks and monitoring production & packaging at the manufacturers, to prevent shortages that may take place and take strict & immediate actions in case of sudden shortages.
• Receiving public complaints about drugs in short (via hot-line, written official letters, e-mails) and working on solving those complaints.
• Manufacturers and Importers support to solve their CAPA related problems that lead to drug shortages.
• Reporting urgent and complicated drug shortages issues to decision makers.
• Issuing Periodical drug shortages bulletin.
• Predict and therefore prevent the occurrence of any shortages.

مجال الشركة:
صناعة الدواء
الدور الوظيفي:
إدارية

Freelance Regulatory Affairs & Business Development Advisor

ديسمبر 2012 - نوفمبر 2014

Freelance

القاهرة، مصر

ديسمبر 2012 - نوفمبر 2014

• Preparing soft and hard registration dossiers for imported and local products (pharmaceutical, cosmetics, food supplement and disinfectants)
• following up all the stages of registration with the Competent governmental authorities till obtaining the registration licenses
• Cooperate and communicate with the different competent authorities due to a long fruitful relationship with most of governmental authorized stuff in the following places.
• Submitting and issuing of the import plans and permits from the competent authorities
• Following up the final release of pharmaceuticals.
• Making suggestions to improve the performance by identifying the areas that need enhancement and ways to achieve that.
• Making suggestions for new product submissions.
• Collect data and prepare submissions to regulatory agencies
• Identifies trendsetter ideas by researching industry and related events, publications, and announcements; tracking individual contributors and their accomplishments.
• Locates or proposes potential business deals by contacting potential partners; discovering and exploring opportunities.
• Screens potential business deals by analyzing market strategies, deal requirements, potential, and financials; evaluating options; resolving internal priorities; recommending equity investments.
• Develops negotiating strategies and positions by studying integration of new venture with company strategies and operations; examining risks and potentials; estimating partners' needs and goals.
• Closes new business deals by coordinating requirements; developing and negotiating contracts; integrating contract requirements with business operations.
• Enhances organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.

مجال الشركة:
صناعة الدواء
الدور الوظيفي:
إدارية

Member of the Technical Office Team

مارس 2012 - نوفمبر 2012

Central Administration for Pharmaceutical Affairs, MOH

القاهرة، مصر

مارس 2012 - نوفمبر 2012

• Providing different studies and policy analyses needed for decision making, policy formulation, necessary regulations development and their implantations.
• Provide technical assistance for development, implementation and monitoring of national medicines policy and strategic plan.
• Provide technical and decision support to different departments to solve problems and simplify procedures for better responsiveness to clients.
• Formulated the new pharmaceutical policy that addressed the emerging challenges in the pharmaceutical field on the regional and international level.
• Reviewed and implemented the new regulatory framework including registration, pricing, supply chain and importation regulations.
• Studied and analyzed issues and documents referred by the head of CAPA and presented recommendations.

مجال الشركة:
صناعة الدواء
الدور الوظيفي:
إدارية

Registration Specialist

يونيو 2009 - فبراير 2012

Central Administration for Pharmaceutical Affairs, MOH

القاهرة، مصر

يونيو 2009 - فبراير 2012

• Preparing issues referred by companies for presenting on technical committee, including issues from all departments at CAPA.
• Reception &Evaluation of the New Human Drug Applications.
• Data entry for the new application.
• Revise and manage the data base for the registered human drug
• Sharing in the legislation and implementation of the new regulations and decrees at the current time

مجال الشركة:
صناعة الدواء
الدور الوظيفي:
إدارية

التعليم

pharmacy

يونيو 2008

يونيو 2008

بكالوريوس، pharmacy

مصر

Skills

Regulatory Affairs
Expert
Regulatory Affairs
Expert
Hard worker
Expert
Hard worker
Expert
Able to concentrate under stress
Expert
Able to concentrate under stress
Expert
Responsible
Expert
Responsible
Expert
Regulatory Affairs
Expert
Regulatory Affairs
Expert

اللغات

الانجليزية

متوسط

العربية

اللغة الأم

الالمانية

مبتدئ

التدريب و الشهادات

الشهادات
ICDL
Mar 2010
eCTD
Oct 2012

التدريب
Assertive Communication skills
MERL
Apr 2011