Adel Mohammed Al-edkawy

QC Deputy managerFull Time

• Job Details:* Develop and approve the company’s quality control policies and procedures based on local and international standards and measures for pharmaceutical industry, taking into consideration internal operating conditions. * Continuous communication and cooperation with the concerned departments to ensure the achievement of management objectives such as quality assurance management, research, product development, production, finance, Supply and chain, Finance... etc. " Follow up sampling & analysis processes performance for routine & stability testing, and ensure its adherence to relevant described methods, existing procedures and maintains GLP, safety, good -housekeeping regulations, and ensure Q.C document’s GMP compliance. * Review certificates of analysis for material, product release, and stability testing and delegated to approve all certificates on behalf of the QC Manager. * Takes decisions for more OOS/OOT investigations & deviations, if needed, under supervision of Q.C. Manager. * Issue, update, & revise the required SOP’s for the different activities carried in Q.C department. * Follow up calibration program for all Q.C Instruments, and ensures commitments to calibration due dates. * Supervise good handling and proper operation of lab. Equipment & instruments, and ensures best equipment utilization. * Follow up the performance of department employees, provide assistance and advice, provide necessary internal or external training in cooperation with HR Department, and approve performance reports and promotion plans. * Management and organization of archives and organized databases for administration to maintain data and files of analysis, quality and release credits to other important data and to ensure the confidentiality of the data and the access to it only by the persons concerned. * Applying quality and ISO instructions internally in management laboratories, operating methods and internal analysis to qualify all laboratories to obtain quality certificates for control laboratories. * Follow-up to the directives and instructions of the Ministry of Health regarding quality and drug manufacturing, and fulfilling its requirements in terms of preparing samples and submitting reports or statistics, etc. * Participate in the evaluation of suppliers and make necessary reports on technical problems from each supplier.

Q.C section head (Q.C Deputy Manager)Full Time

• Job Details:Follow up sampling & analysis processes performance for routine & stability testing, and ensure its adherence to relevant described methods, existing procedures and maintains GLP, safety, good -housekeeping regulations, and ensure Q.C document’s GMP compliance. * Review certificates of analysis for material, product release, and stability testing and delegated to approve all certificates on behalf of the QC Manager. * Takes decisions for more OOS/OOT investigations & deviations, if needed, under supervision of Q C Managersupervision of Q.C. Manager. * Issue, update, & revise the required SOP’s for the different activities carried in Q.C department. * Supervise good handling and proper operation of lab. Equipment & instruments, and ensures best equipment utilization. * Follow-up to the directives and instructions of the Ministry of Health regarding quality and drug manufacturing, and fulfilling its requirements in terms of preparing samples and submitting reports or statistics, etc.

R&D Methodology and stability section headPart Time

• Job Details:Responsible for method of analysis preparation for trial samples and finished products. Responsible for Validation study of active ingredients for trial samples and finished products. Responsible for follow up of accelerated and long term stability samples. Responsible for preparation of validation and stability protocols to ministry of health