• Receive the yearly / quarterly sales forecast.• Study the sales forecast taking into consideration the available lines capacity and the available stocks of finished goods and raw & Packaging materials.• Set plans for production and for materials supply.• Review MRP on a regular basis and place purchase orders accordingly to ensure orders / supplies are in line with the production plan.• Insure proper alignment of the planned purchasing orders taking into consideration the minimum order quantities, lead time,…..etc.• Work closely with local / foreign purchasing to ensure having the materials on time.• Coordinate the new products launches process by working closely with Marketing ,Production, R&D, & Purchasing..• Responsible for coordinating any toll manufacturing by submitting / receiving all kind of information between the company and the client.• Follow-up on all production lines ensuring the production is following the preset production plan.• Conduct regular meetings with production / sales to address all open issues.• Follow-up regularly on the other department (Q.C. for under inspection items, Purchasing for open P.O., Warehouses for storage capacity ..etc )• Issue a quarterly report showing the actual production vrs sales forecast• Review and suggest ways to improve the current flow process

• To ensure the quality of raw materials, packaging materials and finished products are compliant with the approved specifications and GMP/GLP.• Maintains a controlled documentation system in the quality control department.• Monitors compliance with the requirements of approved procedures.• Reviews of quality control records.• Ensures that the proper monitoring and the maintenance of department premises and equipment are done properly.• Ensures that the Monitoring of the calibration program of equipment is done.• Checks the Laboratory organization (For example; document, glassware, chemicals, and equipment).• Ensures the organization and proper keeping of retained samples in the retained samples room.• Ensures the proper handling of reference and working standards.• Ensures the Monitoring of the retention of the QC records.

• Monitor inventory• Coordinate shipping logistics• Ensure accurate documentation• Prepare reports on supply chain performance• Communicate with stakeholders• Enforce strict adherence to safety standards

As a quality control Manager during start up of Unimack International group company , passing NFSA audit for factories white list approval and IMS ISO 9001, ISO 22000,ISO 14001, ISO 45001 and food GMP ISO 22002 part IConducting a gap analysis for the requirements of IPC, QC, and microbiology laboratories.Responsible for direct management and utilization of laboratory (analytical and microbiology), water treatment, sanitation, microbiological equipment, raw materials, and all quality processes.Write, update, and maintain SOP's (Standard Operating Procedures).Leads the development and implementation of Food Safety Fundamentals, the Food Safety Plan and Food Quality Plan.Communicate to relevant personnel all information essential to ensure the effective implementation and maintenance of SQF.Accountable for a safe working environment through the development of strategies focused on accident reduction as well as energy and waste minimization.Optimize resources while ensuring raw materials and finished product meet specifications and manufacturing standards and in accordance with GMP's, HACCP, and all other governmental policies, procedures, and regulations.Ensure application of best practices and signature tools to optimize Efficiency and Effectiveness.Ensure implementation and compliance of all food safety quality and regulatory policies and practices at assigned location.Analyze, review and interpret food safety quality and regulatory policies and practices to identify and drive continuous improvement efforts.

•Coordinating and supervising the day-to-day inspections and analysis of incoming raw materials, and finished products to ensure adherence to specifications and company quality & regulatory standards•Review QC laboratory data for validity and accuracy according to cGMP/cGLP standards•Review documents as a QC department subject matter expert (SME)•Support laboratory investigation of OOS/ invalid assays, CAPAs and change controls•Ensuring accuracy and completeness of executed analytical method qualification, validation, and transfer activitiesSet testing priorities and manage work assignments•Interpreting and enforcing all quality procedures for QC personnel. Ensure staff training qualification for the assigned activities and training completion in a compliant state•Implementing quality control programs to ensure reliability of testing procedures, proper function of laboratory equipment, and compliance with applicable regulations.•Preparing, approving and maintain applicable records. Develops and implements Quality related documents including control plans, visual aids, and work instructions. Recommends changes in specifications of materials, parts, and products based on inspection results. May formulate and revise quality control policies and procedures.•Supporting in troubleshoots problems around quality to come up with solutions that are comprehensive and higher quality in investigation and follow-up. Reviews reports and confers with quality assurance, production, management, and engineering personnel to solve work-related problems.•Ensures full adherence to data integrity and good documentation practices.

•Ensure ERP system meets business requirements and goals and fulfills user requirements.•Key User