Company founderOverall project management: - Financial monitoring - Manufacturing area development - Suppliers contact and raw material order Recruiting, training and development of staff

- Preformulation, formulation of generics- Application of a new method of preformulation (SEDEM method)- Development and validation of assays and stability indicator method- Scale-up and pilot batch manufacturing- Manufacturing process validation- Preparation of the Marketing Authorization Application (CTD format)- Supervision of pharmacy interns in training in the laboratory.

- Daily Validation of sterilization cycles and traceability control- Management of the sterilization process under the responsibility of the pharmacistresponsible for the sterilization sector- Participation in continuous quality improvement (development of policy quality ofservice, management of non-compliant MD, implementation of preventive andcorrective measures, evaluation of customer satisfaction (OR of UH and otherhospitals), updating procedures and work… Show more - Daily Validation of sterilization cycles and traceability control- Management of the sterilization process under the responsibility of the pharmacistresponsible for the sterilization sector- Participation in continuous quality improvement (development of policy quality ofservice, management of non-compliant MD, implementation of preventive andcorrective measures, evaluation of customer satisfaction (OR of UH and otherhospitals), updating procedures and work instruction)- Monthly monitoring of hemodialysis water and updating the control procedure- Environmental Monitoring and updating control procedures- Validation of parenteral nutrition prescriptions, preparation and control of nutritionbags (one week / month)- Night guard (provision of emergency drugs, clinical trials, preparation of parenteralnutrition bags)- Technicians and pharmacy interns training Show less

- Daily Validation of sterilization cycles and traceability control- Analysis of daily records of non-compliance and implementation of corrective actions- Update procedures- Implementation of internal and external audits- Environmental control- Study of the profitability in case of outsourcing sterilization in a private company.- Traceability of implantable MD and monthly monitoring of stocks and implementationof different notebooks care.- Technical assessment of… Show more - Daily Validation of sterilization cycles and traceability control- Analysis of daily records of non-compliance and implementation of corrective actions- Update procedures- Implementation of internal and external audits- Environmental control- Study of the profitability in case of outsourcing sterilization in a private company.- Traceability of implantable MD and monthly monitoring of stocks and implementationof different notebooks care.- Technical assessment of consumables for sterilization- Toxicology: drug dosage (one week per month)- Night guard (provision of emergency drugs, clinical trials, preparation ofchemotherapy bags, clinical trial management and drug dosage)- Technicians and pharmacy interns training Show less

- Validation of chemotherapy prescriptions (CHEMO ® software), organization ofchemotherapy bags preparation, preparation of chemotherapy bags using a negativepressure pharmaceutical isolator, validation of finished preparations.- Daily management of non-compliance and implementation of corrective actions- Environmental control- Management of subcontractors- Management of clinical trials- Update procedures- Qualification of an external unit for manufacturing… Show more - Validation of chemotherapy prescriptions (CHEMO ® software), organization ofchemotherapy bags preparation, preparation of chemotherapy bags using a negativepressure pharmaceutical isolator, validation of finished preparations.- Daily management of non-compliance and implementation of corrective actions- Environmental control- Management of subcontractors- Management of clinical trials- Update procedures- Qualification of an external unit for manufacturing chemotherapy bags Show less

- Control of raw materials, packaging components, intermediate products and finishedproducts and their release- Evaluation of assay methods and procedures and proposal of amendment to thedevelopment department.- Development of a stability indicating Method of levomepromazine

- Daily Activity: technicians aid in various manufacturing tasks that allowed me toacquire a good knowledge of various manufacturing processes drugs.- Ensure implementation of production programs and procedures in accordance withGMP, ISO standards and safety regulations.- Participation in the validation of manufacturing processes of pasty forms.- Control of anomalies and proposal of corrective actions

Pharmaceutical hospital management