-Reviewing & setting company general policy of compliance with the target Quality Management Systems of the international reference standard regarding to the organization context.-Starting with Food Manufacturing company business model (Ferdas for Couscous & Pasta) for Setting, Documentation & Application of an Integrated Management System - QOHSE (ISO 9001:2015, ISO 45001:2018, ISO 14001:2015) in addition to Food Safety Management System (ISO 22000:2018).-Coordinating with company Assigned OHSE Heads for Documentation & reviewing Occupational Health, Safety & Environmental Procedures complying with the updated international standards.-Leading a team for Process tracking & monitoring for setting & application of a well-designed, Risk management – based & integrated HACCP Plan regarding FSMS requirements & procedures.-To set & lead application of cGXP regarding FSMS & management Policy (cGHP, cGMP, cGSP, cGDP, cGLP).-To set & ensure Risk-based system procedures that minimizes, reduces business risks & enhances good opportunities.-Fulfilling a complete PDCA cycle model for the company MS Procedures.-Leading & applying company Internal Auditing Procedure with the assigned team & handling of external auditing procedures with the approved 3rd parties.-Following up – with the assigned company Heads & QA Team – NCRs Monitoring, Reporting, Analysis & appropriate CAs taken.-Coordinating with company Heads & Top Management for Applying Management Review Procedures (Inputs review, Outputs issuance, Decisions & Improvement suggestions taken).-Setting MS General policy & Procedures for sister companies of the holding group of different product categories (Feed, Flour, Cake, Diapers…).

Handling & maintaining both certification & implementation of QHSE management systems (ISO 9001:2015, ISO 14001:2015 & ISO 45001:2018).Assigned Quality Manager of the testing lab accredited ISO 17025:2017.Handling of company audits (Internal, External & Supplier ones).Setting & maintaining product / process / service compliance with regard to both regulatory authorities & customers’ requirements.Evaluation of Continuous Improvement measures by monitoring & control of PDSA cycle of company / system (deviations, internal NCRs, external customer complaints, RCA, CAPAs, Change Control & Risk management procedures).Monitoring, analysis , control & eliminating root causes of company product returns.

-Setting quality Objectives, Policy, Plans & Procedures with regard to company objectives.QMS implementation with regard to ISO 9001:2015 & Cosmetics GMP ISO 22716:2007.-Optimizing products’ compliance by applying GMP guidelines in cosmetic industry (ISO 22716:2007) in the whole site processes; from start (Incoming materials supply chain) to the end (Finished goods distribution into the market).

•Ensures product compliance to the approved design & reference specifications required by the customer throughout 3 production shifts by daily controlled reporting system.•Traces technical NCRs in production sites for leading the investigations & following up the initiated CAPAs plan with the concerned departments.•Ensures the final product release upon completeness of all required actions (IPC, FP inspection, COA, dispatch inspection…).•Ensures & maintains all communications required among QC, IPC, Production & QA members to stabilize all processes' parameters & specifications at the operations site.•Leads the investigations of customer complaints in close coordination with QA members, Technical Operations Manager & other concerned departments heads to take the appropriate CAPAs plan in the most appropriate time.•Handles & manages all customer's & third parties' audits.•Passing surveillance audits for ISO17025/2005 & ISO 9001/2008 . •Follow up internal auditing & site inspection findings & appropriate CAPAs progress.•Reporting all audits' findings, action plans & areas for improvement to the Managing Director.• Maintaining the department manpower by staffing high calibers & reorganization of working teams.

•Establishment of new documentation system with regard to cGMP & regulatory authorities' guidelines (BPR, SOPs, Policies, Quality Checklists…. etc.).•Applying an IPC procedure in all production areas to for monitoring & control of standard procedures.•Reviews & ensures compliance to cGMP in the whole site (M/C qualification, Calibration, Clean Areas' Validation, and Process Validation).•Reviewing & updating WH procedures for incoming materials' receiving, storage & release.•Ensures & traces the implementation of deviations, NCRs & CAPAs management procedures in the site.•Final approval for finished products' release upon reviewing compliance & completeness of all required actions & documents.•Conducts training for all the concerned departments on cGMP, newly issued SOPs and products' Batch Production Records.•Conducts on job training for QA Specialists on IPC, GSP, GLP, internal auditing & self inspection.•Passing MOH site audit for license of Liquid Dosage Form production line.

Monitoring and supervision of all Quality Assurance activities in the plant (IPC, Batch record review, Validation, Auditing, Documentation, etc.). Ensuring the effectiveness of Quality Assurance monitoring for the whole production process that meet quality standards specified. Process verification and SOPs writing for the technical departments of the plant. Conduct planned and unplanned internal audits as a member of the internal audit team. Interact with departments' Section Heads and Supervisors to co-ordinate different activities affecting the process quality. Ensuring, with all QA Specialists, the compliance of cGMP in all processes carried out. Ensuring QMS effectiveness & compliance with ISO 9001\​2008 with regard to Alandalous quality policy.

Inspection of manufacturing operations to ensure compliance with cGMP and other regulatory requirements. Participating in process validation & cleaning validation in production areas. Validation for new production areas & following the different qualification stages (IQ, OQ.& PQ) of new production machines. Compressed air filters validation (capsule filters type). Checks and co-ordinates quality requirements among production and other departments. Assist in regulatory inspections. SOPs writing for different QA devices and testing procedures. Reviewing deviations & investigation reports to ensure that root causes have been identified and appropriate corrective actions have been implemented. Organizing & co-ordinating QA Specialists' activities and responsibilities throughout different working shifts (day and night shifts).

IPC inspection in Liquid and Semisolid dosage forms. Promoted upon KPIs achievements to Solid dosage form IPC team. Random check test throughout processes for critical start up tests. Reviewing batches’ records for completeness, correctness and compliance to in-process control results with specification and reporting of unusual incidents. Using spectrophotometric methods, colourimetric methods and other analytical methods for active material detection between different products. Reporting data for all processes carried out.