• Overseeing and coordinating analytical research, as well as formulation and process development teams.• Establishing and effectively managing a new R&D development unit in Amman.• Enhancing quality systems and refining development approaches.• Ensuring registered files are updated to comply with GCC and restricted markets regulations.• Taking charge of development and technology transfer initiatives for solid, liquid, and steriledosage forms.• Conducting product selection and feasibility studies.• Effectively managing CAPEX and budgets.• Supervising the development of oral solid dosage forms, sterile dosage forms, and oral liquiddosage forms.• Establishing strong relationships with authorities in both internal and external markets.• Identifying and resolving issues related to existing products through effective troubleshooting.

• Overseeing and coordinating analytical research, as well as formulation and process development teams.• Establishing and effectively managing a new R&D development unit in Amman.• Enhancing quality systems and refining development approaches.• Ensuring registered files are updated to comply with GCC and restricted markets regulations.• Taking charge of development and technology transfer initiatives for solid, liquid, and steriledosage forms.• Conducting product selection and feasibility studies.• Effectively managing CAPEX and budgets.• Supervising the development of oral solid dosage forms, sterile dosage forms, and oral liquiddosage forms.• Establishing strong relationships with authorities in both internal and external markets.• Identifying and resolving issues related to existing products through effective troubleshooting.

• Spearheading the formulation and process development activities for oral and injectableproducts across EU, US, and MENA markets.• For oral dosage forms, overseeing the development of immediate release, modified release, andmultiarticulate systems.• For injectable products, leading the development of simple sterile liquids (vials and bags),lyophilized powders, and injectable suspensions.• Taking charge of technology transfer initiatives for injectable products.• Leading technology transfer efforts for oral dosage forms to Algeria and other contractmanufacturing organizations (CMOs) within the MENA region.• Providing training to the R&D team on development approaches utilizing Quality by Design (QbD)tools.• Collaborating within a committee responsible for introducing new technologies within the MSPharma group.• Preparing Standard Operating Procedures (SOPs) related to R&D, technology transfer, andproduction.• Establishing and monitoring budgets for new drug product developments and other R&D-relatedcapital expenditures (CAPEX).• Managing operational expenditures (OPEX) for the R&D team.• Collaborating with the business development department to assess the feasibility of projects.• Evaluating the technical feasibility of new products based on their applicability at both R&D andproduction sites.• Conducting audits of in-licensing files and assessing their technical suitability.• Delivering progress updates and reporting any delays in R&D projects to management.• Coordinating in vivo studies with various Contract Research Organizations (CROs).

• Plan and oversee the construction of new R&D laboratories for the development of oral andinjectable dosage forms.• Lead formulation and process development activities for oral and injectable products targetingEU, US, and MENA markets.• Develop oral dosage forms such as immediate release, modified release, and multiarticulatesystems.• Develop injectable products including simple sterile liquids (vials and bags), lyophilized powders,and injectable suspensions.• Take charge of technology transfer processes for injectable products.• Manage technology transfer processes for oral dosage forms to Algeria and other CMOs in theMENA region.• Provide training to the R&D team on development approaches using QbD (Quality by Design)tools.• Collaborate within a committee responsible for the introduction of new technologies within theMS Pharma group.• Prepare standard operating procedures (SOPs) related to R&D, technology transfer, andproduction.• Develop and monitor budgets for new drug product developments and other CAPEX (capitalexpenditure) related to R&D.• Manage OPEX (operating expenses) for the R&D team.• Collaborate with the business development department to assess project feasibility.• Evaluate the technical feasibility of new products based on their workability at R&D andproduction sites.• Conduct audits of in-licensing files and assess their technical suitability.

• Technology transfer for injectable products from MS pharma Injectable to MSPharma Turkey.• Technology transfer of oral dosage forms to Algeria.

• Lead the development of oral dosage forms specifically designed for the MENA and US markets.• Actively contribute as a member of the Fast Track Committee, focusing on high-value products.• Conduct scale-up studies to ensure successful transition from formulation development tocommercial production for the developed products.• Oversee and coordinate the progress of bioequivalence studies, ensuring compliance withregulatory requirements.• Drive innovation by researching and working on new drug delivery systems, with a primaryemphasis on multiarticulate systems.• Collaborate closely with Glatt Company in the co-development of drug products, leveraging theirexpertise and resources to achieve mutual success.

Scale up and process development team.Responsible for studying the scale-ability of projects from R&D scale into pilot and production scale.process improvement and trouble shooting.Formulation development for problematic products.

Development of co-processed exipients , DPI formulations , Active layering using Wurster fluid bed coater , and using spray drying to improve physicochemical properties of some drugs .

Teaching assistant at pharmaceutics Dept. Where I gave physical pharmacy , dispensing of dosage forms , pharmaceutical technology and pharmacokinetics courses.