Hire the Best Quality Assurance in Ad Dammam, Saudi Arabia

Specialties: HACCP, On job training, Experience by facing client auditing (Saudi Aramco), Preparing Presentations, Preparing Checklists.

My ambition is to join in a professional work environment with belonging, seriousness sacrifice and patience to work so that we can develop skills, achieve goals and vision to be happy with excellence, progress and effective development

An excellent Quality Assurance & Validation Manager with 22+ years of experience in the pharmaceuticals field. Managed quality for multiple pharmaceutical manufacturing companies. A steadfast leader that helped start a new pharmaceutical factory from scratch. Managed to obtain an EMEA Certificate of GMP Compliance of a non-European manufacturer as the first and the only pharmaceutical manufacturer to receive such a certificate in Egypt. Manage all validation activities related to production equipment & cleaning/manufacturing/packing processes, which include the development, writing, execution, review, and approval of validation plans, validation protocols, and reports (DQ/FAT/SAT/IQ/OQ/PQ/VSRs), etc. Strategically manages any problem or complaint and finds a solution for them. A strong leader that incorporated revolutionary technological advances within the pharmaceuticals field to improve customer experiences. Achievements: - Responsible for Initial Validation and qualification of the Sterile Area Expansion and new production line project - Preparing for “EMEA” Certification and Technology Transfer Leader of the Certified Product from ATHLONE (Ireland) to MAP (Egypt) - Participate in starting a new pharmaceutical factory and manufacturing site (for sterile and non-sterile products). - Contributed to Acquiring the European Certificate “EMEA” for a non-European Pharmaceuticals manufacturing site - Help a company obtain the first and only pharmaceutical manufacturer to obtain such a certificate in Egypt. Expertise: Quality Management | Change Management | Corrective/Preventive Actions | Internal/External Audit | Regulatory Compliance | Process Validation | Cost Estimation/Forecasting | Standard Operating Procedure (SOP)| Strategic Planning | Client & Suppliers Relationships | Cross-functional Team Leadership | Validation Management cGMP manufacturing · Risk Assessment |Strategic Planning |Sop |GMP |Pharmaceutical Industry |Validation |Regulatory Affairs |Quality System |GLP |FDA |Quality Assurance |CAPA |Compliance |Quality Auditing |GxP |Change Control |Teamwork |ISO 14001 |Problem Solving |Leadership |Quality Improvement |Communication Skills |Time Management |V&V |Quality Control |Cleaning Validation |Calibration |Pharmaceutics |Quality Management |Aseptic Processing |Regulatory Requirements |Regulatory Submissions |Batch Release |Deviations |Deviation Management |ISO |Software Documentation |USP |TQM |cGMP practices |ISO 9000

An excellent Quality Assurance & Validation Manager with 22+ years of experience in the pharmaceuticals field. Managed quality for multiple pharmaceutical manufacturing companies. A steadfast leader that helped start a new pharmaceutical factory from scratch. Managed to obtain an EMEA Certificate of GMP Compliance of a non-European manufacturer as the first and the only pharmaceutical manufacturer to receive such a certificate in Egypt. Manage all validation activities related to production equipment & cleaning/manufacturing/packing processes, which include the development, writing, execution, review, and approval of validation plans, validation protocols, and reports (DQ/FAT/SAT/IQ/OQ/PQ/VSRs), etc. Strategically manages any problem or complaint and finds a solution for them. A strong leader that incorporated revolutionary technological advances within the pharmaceuticals field to improve customer experiences. Achievements: - Responsible for Initial Validation and qualification of the Sterile Area Expansion and new production line project - Preparing for “EMEA” Certification and Technology Transfer Leader of the Certified Product from ATHLONE (Ireland) to MAP (Egypt) - Participate in starting a new pharmaceutical factory and manufacturing site (for sterile and non-sterile products). - Contributed to Acquiring the European Certificate “EMEA” for a non-European Pharmaceuticals manufacturing site - Help a company obtain the first and only pharmaceutical manufacturer to obtain such a certificate in Egypt. Expertise: Quality Management | Change Management | Corrective/Preventive Actions | Internal/External Audit | Regulatory Compliance | Process Validation | Cost Estimation/Forecasting | Standard Operating Procedure (SOP)| Strategic Planning | Client & Suppliers Relationships | Cross-functional Team Leadership | Validation Management cGMP manufacturing · Risk Assessment |Strategic Planning |Sop |GMP |Pharmaceutical Industry |Validation |Regulatory Affairs |Quality System |GLP |FDA |Quality Assurance |CAPA |Compliance |Quality Auditing |GxP |Change Control |Teamwork |ISO 14001 |Problem Solving |Leadership |Quality Improvement |Communication Skills |Time Management |V&V |Quality Control |Cleaning Validation |Calibration |Pharmaceutics |Quality Management |Aseptic Processing |Regulatory Requirements |Regulatory Submissions |Batch Release |Deviations |Deviation Management |ISO |Software Documentation |USP |TQM |cGMP practices |ISO 9000

Seeking a challenging position in a reputed organization where I can learn new skills, expand my knowledge, and leverage my learnings.

Motivated Quality Manager Assistant with a Bachelor’s Degree in Industrial Engineering and Management. Capable of developing, implementing, and periodically evaluating a program to ensure the organizations' production operations, from raw materials to finished products, meet the quality, integrity, and efficiency standards set by the organization. Supported by a demonstrated ability to lead a high-performance team, encourage them, and consistently meet critical criteria with excellent analytical and troubleshooting skills. Equipped with a Radiation Safety Officer (RSO) Certificate, and an Organizational Development course. All of that led me to implement a reverse osmosis plant with 200 M3/Hour, as well as lead 36 to 48 employees during 3 shifts.

Quality Manager Assistant with over 17 years of experience in developing, implementing, and periodically evaluating a program to ensure the organizations' production operations, from raw materials to finished products, meet the quality, integrity, and efficiency standards set by the organization, which enriched my field expertise in: - Quality Assurance - Quality Management - Quality Control - Risk Management - Project Management Holding a Bachelor’s Degree in Industrial Engineering and Management, and a Diploma in Mechanical Technical Production, in addition to that, I believe that the only way to stay relevant is to keep learning, so every week I strive to pick up at least one new technique that I can work into my technical skills such as: - Internal Auditing Training Based on ISO 50001: 2018 (EnMS) - Quality Assurance - Organization Excellence All of the above helped me to make significant success in managing projects and achievements successfully such as: - Oversee and plan for Capital Expenditures (CapEx) and Operating Expense (OpEx) along with full control to achieve cost reduction - Reduced the chemicals cost by about 20% under control It's going to be my absolute honour to continue my career with your organization. I'm a very professional individual who is eager to give 100% of his energy and concentration and willing to learn, I always try my best to exceed your expectations no matter what. Feel free to contact me via mail, or private msg. Hussain A. H. Al-Mahfooz Hussain.mahfooz@icloud.com +966504974124

Experienced Food Safety, Quality Assurance, Health and Environment Specialist with a demonstrated work history in Restaurant, Industrial Catering and Airline Catering. I skilled in Food Safety Management System, Food Production, Operations, ISO Standards, HACCP, FSSC, FSMS, HALAL, CCPs, PRPs, OPRPs, GMPs, Research and Development (R&D), and Total Quality Management (TQM). My objectives are to grow with the organization, not just as a professional but also as an individual, be mentored by the best, be valued and in return contribute significantly to the organization's objectives every day through sheer hard work and dedication. To get a respectable position in a dynamic organization where I can utilize my potential and prove myself as an asset for that organization.