My current Job Description includes:• All regulatory issues of CIRA Pharma Group in addition to its 8 sister companies.• Registration of new Cosmetic Products (Local & Imported).• Registration of new Dietary Supplements products (Local & Imported).• Registration of new Pharmaceutical Products (Local).• Re-registration of expired products of the companies.• Signing & Legalization all Toll Contracts with different plants & others related to CIRA’s Plant.• Cooperating with Research & Product Development & Marketing Sectors in selecting / developing company's products.• Revising/editing the scientific data of the companies’ products related to inner & outer labels.• Co-operation with the Designer Director & Printing Houses in preparing and reviewing all the data before printing.• Co-operation with Supply Chain Director, Plant Manager, Q.C. Manager & Q.A. Section Head in preparing & handling Plant’s & Products’ Inspection.• Handling all issues related to EDA (Egyptian Drug Authority) & NFSA (National Food Safety Authority), including Registration, Inspection & Licenses departments.• Leading & Developing a team of 2 Section Heads & 1 Senior Regulatory Affairs Specialist.• Highly effective member in a committee concerns with preparing CIRA’s Plant till issuing the Plant License from EDA (Egyptian Drug Authority) & IDA (Industrial Development Authority).

Job Description:• Registration of new cosmetic products (Local & Imported) - (Total No. of Registered Products is 210)• Re-registration of expired products of the company.• Cooperating with research and development department & marketing department in selecting / developing company's products.• Responsible for all the scientific data of the company products' inner & outer labels.• High co-operation with the Designer Manager, Printing House, Companies responsible for making tubes & stickers in preparing and reviewing all the data before introducing the products' to the market.• Cooperating with Plant Manager, Export Manager, Import Manager & Quality Assurance Manager.• Responsible for all communications related to M.O.H. Registration, Inspection & Licenses departments. • Preparing registration files, free sales & G.M.P. certificates for exported products.• Preparing registration files for the company’s products in (Saudi Arabia, Sudan, Palestine, Iraq, Tanzania, Kuwait & Ghana) according to each country requirements.

* Member in a committee specialized in preparing, translating, and revising final English leaflets, Arabic leaflets, and external packs prior to its submission to the market.* Member in the "Planning / Production Committee".* Preparing / executing contracts of Bioequivalence Studies.* Attending pricing committees in Drug Policy & Planning Center.* Registration of the new pharmaceutical products.* Re-registration for expired products of the company.* Preparing pricing files for newly submitted products.* Preparing the annual production plan for the active & inactive ingredients needed for the production of the registered products.

* Achieve allocated sales target.* Solving problems found in the assigned territory (Shoubra El Khema, Shoubra, Ramsis, Down Town, Sayeda Zeinab, Masr El Kadima, Maadi, and Helwan).* Leading a team of 7 Medical Representatives & responsible of following up the achievement of their target.