MOHAB Amin Eldesouki

Quality Assurance ManagerFull Time

• Job Details:Egypt OTSUKA is the major manufacturer of LVP in Egypt, it’s an affiliate of OTSUKA PHARMACEUTICAL JAPAN.  Overall responsibility for all Quality Assurance activities in the site.  Responsible of managing QA department by aligning daily tasks to organization objective & allocating resources to achieve such objectives.  Responsible for batch records review.  Manage & control process validation, equipment qualification for all products & systems at the site.  Handling of deviations, failure investigation, product quality review, returned goods.  Management & coordination of Internal audit program.

Quality Control ManagerFull Time

• Job Details: Ensure efficient transfer of analytical methods from Contract giver sites ( Novartis, GSK, J&J, Biofarma) to Arabio site .  Part of new product introduction committee participating in technology transfer process.  Coordinate with contract giver to identify gaps that may represent hurdle during project progress pertained to QC testing.  Implementing Team dynamics to build up strong QC team to achieve organisation objectives.  Managing department different related activities & ensuring availability of adequate resources to achieve departmental objectives.

Quality Control ManagerFull Time

• Job Details: PSI is a manufacturer of large and small volume injectables in different dosage forms.  Successfully spearheading the quality control team consisting of 26 members.  Responsible for managing activities pertaining to quality control of starting materials, in process checks and finished goods.  Managing various tasks related to sampling, specifications and testing with necessary documentation concluded by usage decision against each tested entity.  Maintaining adequate facilities with necessary qualified equipment, trained personnel, validated methods of analysis and approved procedures all encompassed in a suitable environment.  Accountable for site auditing of local packaging materials (PM) vendors, developing business plans to qualify new vendors as well as newly developed PM’s; administering internal auditing of manufacturing facilities and warehouses.  Authorising raw and packaging materials consignments, evaluating analytical records, overseeing approval of quality control documentation and all other activities necessitated by GMP guidelines.  Coordinating with regulatory affairs department for knowledge transfer concerning analytical literature in course of new products registration submissions.  Responsible for review and preliminary approval of quality agreements established between organisation and packaging materials vendors.