Ahmed Mohamed Ali

Results-driven professional with extensive experience in production planning, quality control, and resource management. Expertise in strategic methodologies to optimize operations and enhance productivity across various projects. Proven track record of implementing process improvements that yield significant efficiency gains while fostering a collaborative team environment. Committed to driving organizational success through innovative solutions and effective leadership.

Production Expert with strong background in overseeing manufacturing processes and ensuring operational efficiency. Proven ability to lead teams, optimize workflows, and drive productivity in fast-paced environments. Known for strategic problem-solving, adaptability, and fostering collaborative work environments. Skilled in lean manufacturing, quality control, and resource management.

Results-driven production professional prepared for demanding roles in manufacturing and operations management. Proven track record of enhancing production efficiency and maintaining high-quality standards. Focused on team collaboration and adaptability to changing project needs, with strong skills in process optimization and leadership.

Diligent Production Manager with extensive experience in managing production workflows and optimizing processes for efficiency. Successfully led teams to achieve project milestones and improve operational performance. Demonstrated expertise in resource allocation and process improvement.

Multi-talented Production Manager experienced in diverse industrial environments. Profit-motivated collaborator with ingenuity in troubleshooting complex productivity obstacles. Creative leader with motivational supervisory methods.

Proactive Production Manager successful at anticipating needs and making adjustments to schedules, materials and workflow. Ready to bring expertise to company needing hands-on, knowledgeable and resourceful leader.

Ambitious Production Manager with more than 15 experience years in Manufacturing environments. Motivates employees to align performance with company objectives in fast-paced production environments. Superior competency in resource allocation, production scheduling and workflow management.

Production management professional knowledgeable about allocating resources, optimizing production and increasing output with hands-on and dedicated approach. Articulate and professional problem-solver with good relationship-building abilities. Proficient in planning and implementing innovative production strategies.

Smoothly direct employees carrying out Processing and Packaging operations to achieve demanding production goals, schedules and budget targets. Driven leader with excellent analytical, decision-making and project management abilities. Maintain employee focus and achieve quality targets with hands-on supervision.

Experienced Production Manager successful maintaining consistent on-time delivery for customers. Well-organized, proactive and resourceful in dealing with routine and complex production issues.

Skilled Production Worker offering more than 15 experience years in quality, planning, warehouse and manufacturing environments. Focused on being productive and safety-minded at all times.

History of completing safe, accurate and physically-challenging work.

• Responsible Person for SAT for Production Machines in LIPTIS for Pharmaceuticals and Medical Products Plant:
• Cannan Preparation Line.
• Anchor Preparation Line.
• Fette 1200i Compression machine.
• Xaolun Coating Machine.
• MG2 (Alter Nova) Capsule.
• Hoonga V3 Blistering Machine.
• Uhlmann B1330 Blistering Machine.
• Hengi Bottle Filling Line.
• Jekson Track & Trace Printing Line.
• Passing External Audit :
• LIBYA Audit.
• YEMEN Audit.
• IRAQ Audit.
• LEBANON Audit.
• ETHIOPIA Audit.
• KENYA Audit.
• SUDAN Audit.
• TANZANIA Audit.
• UGANDA Audit.
• RWANDA Audit.
• WHO Audit.
• Being a member in Risk Assessment team as a Production Responsible Person in LIPTIS for Pharmaceutical and Medical Products in EGYPT site.
• Being a member in FDA Qualification team as a Production Responsible Person in LIPTIS for Pharmaceutical and Medical Products in EGYPT site.
• Having a delegation of Being Director of Operations in absence of Director of operations and his Deputy.

• Responsible for overseeing production employees in their performance. Insure the production process is flowing smoothly to meet the Company’s profitability.
• Responsible for the technical management, supervision and control of industrial production processes.
• Overseeing the production process, drawing up a production schedule.
• Identify all tasks for teamwork and provide continuous support to all members according to operating standards on every day.
• Ensure that products are produced on time and are of good quality.
• Ensure that the drug products are manufactured properly in accordance with regulations under drug product laws.
• Supervise effective working of production personnel and prepare effective production schedules and ensure compliance to all company policies.
• Administer all work according to QA/QC principles and recommend strategies to improve processes and reduce load.
• Manage and prioritize all production processes and implement all production plans.
• Analyze staffing requirements and ensure efficient compliance to production schedules and budget for all production process.
• Ensure compliance to workplace policies according to safety objectives.
• Supervise strictly implementation of cGMP regulations and SOPs in all aspects of production processes.
• Avoiding errors, mix ups and contamination or cross contamination during processes.
• Ensuring proper calculation of yield and reconciliation and that there are no discrepancies outside the acceptable limits.
• Correcting and/or reporting any deviations and/or discrepancies related to personnel or processes.
• Working out the human and material resources needed.
• Being responsible for the selection of equipment.
• Liaising among different departments, e.g. suppliers, managers.
• Working with managers and departments staff to implement the company's policies and goals.
• Ensuring that health, hygiene and safety guidelines are followed complies with cGMP.
• Reviewing worker performance.
• Approve training needs for production employees.
• Ensure that the required initial and continuing training of production employees is carried out and adapted according to need.
• Approve/Review the batch records and standard operating procedures relating to production operations and to ensure their strict implementation.
• Check the maintenance of the department, premises, and equipment.
• Ensure that the appropriate process validations and calibrations of control equipment are performed and recorded and the reports made available.
• Participate in Self-inspection and External inspections.
• Approve/follow-up the purchasing order issued from production department and follow-up their implantation.
• Ensuring quality, delivery and budget objectives are met.
• Review the regular reports and statistics on a daily, weekly and monthly basis.
• Comply with cGMP and GDP according to WHO organization.
• Toll Manufacturing Follow-up.

• Participate in planning and developing of the production process for all (existing , scale up ,pipeline) products adhering to the highest and updated quality standards and control systems(SOPs , Logs , ERP ,documentation ...) with the effective cross function with all departments to achieve Liptis targets and goals on time and within the preset budget and the effective collaboration in Liptis long term plans and projects(Plant project ,Biotech….)
• Monitor production plan according to the approved forecast with the coordination with supply chain department regarding the readiness of all starting materials 3 months before production.
• Assure with the team, all materials are in the MFG. site and released one month before start production.
• Review and adjust the production plan/schedule when needed and spread data intra departmental.
• Follow up the effective coordination with MFG sites to achieve the production plan on time.
• Reporting and reports analysis for all reports prepared by the production staff/other departments.
• Review and check the CCPs readiness product check list for all working products on weekly basis.
• Participate in establishing and renewing of MFG contracts with the coordination of RA department/R&D department.
• Monitor, investigate deviations, and implement CAPA within the department and within Liptis team.
• Participate in cooperating with Health and Food Supplement inspector and resolve problems if found.

• Overseeing the production process, drawing up a production schedule;
• Ensuring that the production is cost effective;
• Making sure that products are produced on time and are of good quality;
• Working out the human and material resources needed;
• Monitoring the production processes and adjusting schedules as needed;
• Being responsible for the selection and maintenance of equipment;
• Monitoring product standards and implementing quality-control programs;
• Liaising among different departments, e.g. suppliers, managers;
• Working with managers to implement the company's policies and goals;
• Ensuring that health and safety guidelines are followed;
• Reviewing worker performance;
• Identifying training needs.
• Approve the instructions relating to production operations, including the in-process controls, and to ensure their strict implementation.
• Ensure that the production records are evaluated and signed by a designated person;
• Check the maintenance of the department, premises, and equipment;
• Ensure that the appropriate process validations and calibrations of control equipment are performed and recorded and the reports made available;
• Ensure that the required initial and continuing training of production personnel is carried out and adapted according to need.

• Identify all tasks for teamwork and provide continuous support to all members according to operating standards on every day.
• Supervise effective working of production personnel and prepare effective production schedules and ensure compliance to all company policies.
• Administer all work according to QA/QC principles and recommend strategies to improve processes and reduce load.
• Manage and prioritize all production processes and implement all production plans.
• Analyze staffing requirements and ensure efficient compliance to production schedules and budget for all production process.
• Ensure compliance to workplace policies according to safety objectives.
• Supervise strictly implementation of cGMP regulations and SOPs in all aspects of production processes.
• Avoiding errors, mix ups and contamination or cross contamination during processes.
• Ensuring proper calculation of yield and reconciliation and that there are no discrepancies outside the acceptable limits.
• Correcting and/or reporting any deviations and/or discrepancies related to personnel or processes.
• Ensuring that health and safety guidelines are followed.
• Reviewing worker performance.
• Ensure that the required initial and continuing training of production personnel is carried out and adapted according to need.
• Making sure that products are produced on time and are of good quality.
• Follow up for maintenance of equipment and tools.
• Supervise IQ, OQ and PQ for production machines in LIPTIS PHAMACEUTICALS for Pharmaceutical and Medical Products Plant.
• Participate in Start-up of LIPTIS PHAMACEUTICALS for Pharmaceutical and Medical Products Plant.
• Participate in establishing of documentation and system of LIPTIS PHAMACEUTICALS for Pharmaceutical and Medical Products Plant.

• Ensure production area is safe to work, productive and has required inventory.
• Maintain production machines and equipment.
• Ensure equipment and work floor is clean, safe and well-maintenance.
• Monitor and control processes using visual observation, process data and on-line testing.
• Identify and debug problems in processes, products, equipment and work for solution.
• Resolve practical problems and deal with variety of concrete situation variables where limited standardization exists.
• Perform tasks assigned to operations.
• Promote safe and healthy production environment and perform safe work practices always.
• Establish and perform high performance standards characterized by integrity.
• Support field personnel in production data management.
• Lead and direct operators to ensure production integrity.
• Support data management and technical evaluation efforts of team.
• Recommend new approaches to streamline team's data management.
• Supervise strictly implementation of cGMP regulations and SOPs in all aspects of production processes.
• Avoiding errors, mix ups and contamination or cross contamination during processes.

• Issuing for site master file (SMF) of the factory and any technical changes.
• Assuring of implementation Good Manufacturing Practice cGMP.
• Reviewing the standard operating procedure and master documents of quality assurance.
• Supplier auditing & qualification.
• Documentation, issuance, archiving, distribution of master documents and Making database for it.
• Batch revision after the end of the manufacturing & release.
• Deviation investigation.
• Complaints investigation.
• Recall investigation.
• Management review.
• Release of Finished Products.
• Monitoring for reprocessing and repackaging procedures.
• Self inspection.
• Validation & qualification activities.
• AHU & HVAC system, Water system, Machine qualification and calibration program.

• Fluent with good appearance.
• A good negotiator and tactful.
• Able to learn new tasks quickly.
• Ambitious, self-motivated and dynamic.
• Ability to work under pressure.
• Workgroup and management leadership and creative.

• Attended the 2nd training course in First aid and Emergency in the faculty of pharmacy -Assuit University at 04/2006.
• Attended the summer training program in the production department in T3A Company at 07/2006.
• Attended the third training course in clinical pharmacy and first aid at the drug information center - faculty of Pharmacy - Assiut University at 07/2007.
• Attended the PHARMACONEX at 04/2016.
• Attended the "cGMP Compliance Inspection" course at 03/2017 by AGON Academy (FDA Approved).
• Attended the "Handling of Deviation Effective CAPA Strategy" course at 11/2017 by AGON Academy (FDA Approved).
• Attended the "Advanced cGMP and GHP" course at 12/2017 by AGON Academy (FDA Approved).