• Safety variation and renewal submissions to the Health Authorities internationally for Drugs in (Asia/APAC, Latin America, Africa, Middle East and Eastern Europe ). • Preparation of the submission packages in (eCTD, NeeS & ASEAN formats). • Answer to Question from NCA• Permanent contact & coordination with local affiliates • Preparation/redaction of internal procedures (SOP) & Working Practice Document (WPD)• Regulatory Intelligence• Project lead

• Managing production staff• Analyzing failures, malfunctions, propose improvements• Preparing documents: operating, cleaning and maintenance procedures, batch files, manufacturing and packaging instructions, log books...• Ensuring the continuity of the production, from the supply and availability of stocks (raw materials) to the delivery of the final product.• Performing activity reports (dashboards, production reports)

Quality assurance trainee

• Providing information on disease prevention and treatment, drug interactions, and possible side effects of medications• Preparing and maintaining drug inventories, ordering supplies, reviewing drug records, and preparing labels for prescriptions• Educating patients on the proper use of over-the-counter medications such as pain relievers or allergy medications• Explaining the purpose of prescription medications to patients and monitoring their use of the medications• Supervising the fulfillment of prescriptions by pharmacy technicians

• Participation in a clinical trials of bacteriostatic non-UV lamp (Biovitae)• Participation in clinical pharmacy activity: pharmaceutical analysis of prescriptions- conciliation• Management of drugs and medical devices inventories• Monitoring and issuing orders• Analysis of the consumption of antibiotics of the Burn Intensive Care Unit over a period of 6 months