Dates : Jan. 2007 – Till Now Position in Company : Making, Packing and Start up Process Engineering Systems Leader Company Name : (Proctor & Gamble Company) Dammam Plant – Saudi Arabia Company Address : Saudi Arabia
1 Dates : April 2006– Jan 2007 Position in Company : Operation Engineer 2 Dates : June 2003– April. 2006 Position in Company : Central control Room Operator Company Name : Arab Company for white Cement Industry Company Address : Jordan
Dates : Sep. 2001– Dec 2002 Position in Company : Laboratory Technician Company Name : Jordan Carbonate Company Company Address : Jordan
Eductation
Education Information
University Education Institution : Al-Balqa' Applied University Degree: : Bachelors Major : Chemical Engineer Location : Amman-Jordan Date of graduation : Feb. 2006 Grade : 2.89/4.00 (Good)
College Education Institution : Amman College For Engineering Technology (Polytechnic). Degree: : Diploma Major : Chemical Industries Technology Location : Amman-Jordan Date of graduation : July 2001 Grade : 74.7 (Al-Shamel Exam)
Certification
1.Quality Assurance Key Elements(Internal Audit)–Bahrain Oct, 27th – Oct 31st2007 2.Microbiology–Engineering workshop–Saudi Arabia July,1st–July, 2nd20073. Quality Maintenance Workshop–Saudi Arabia–26th Jan 2008–30th Jan 2008 4.Process Control Strategy - Saudi Arabia – 1st March 2007 5.Leading Quality Incident Investigation (LQII)-Saudi Arabia–12th May 2007–13th Jan 2008 6.Quality Incident Elimination Methods (QIEM)-Saudi Arabia–3rdJan2007–4thJan 2007 (2 Days). 7.Process Validation-Saudi Arabia–18th March 2007 8.Quality Window-Saudi Arabia–17thApril2007–18thApril2007 9.Late-Late Product Differentiation Process–Czech Republic-30th March2008–5April2008 10.Total Quality Tools 11.Total Quality Fundamentals 12.Microbiology Daily Management 13.Product Quality Matrix 15.Quality Pillar 16.Self Improvement Procedure 17.Quality Incidents
Additional Information
Standard Documents 1.Originate Formula Cards and Manufacturing Standards. 2.Originate Process Related SOPs. Process Improvement 3.Monitor, update and set all process Conditions and Centrelines. 4.Improve department process capability and operation personnel. 5.Change control revision, approval and follow-up. 6.Lead Process Optimization and Saving Projects. 7.Lead Quality incident, Quality Failures & Process Failures Investigations. 8.Insure all Quality, Microbiology & Safety Systems is applied in any change or improvement in the process Process Control Strategy 9.Develop Process Control Strategy. 10.Review Calibration scheduling, results and approval. 11.Issue Statistical Process Control and Statistical Quality Control Reports and Analyzing Data. Validation 12.Review and Approve IQ, OQ, PQ protocols and reports for systems, utilities and equipment. 13.Review and Approve Cleaning and Sanitization Protocols. 14.Contribute on commissioning, Qualification & Verification for new projects and formulas. 15.Originate Validation Master Plan & Master List. Process Study 16.Contribute on Process Safety Study (PSS). 17.Contribute on Process HAZOP Analysis (PHA). 18.Contribute on Product Quality Trade Survey. 19.Contribute on Process Design Reviews. 20.Contribute on qualifying new Raw Material Suppliers. 21.Contribute on Microbiology Risk Assessment. 22.Lead Vendor Acceptance Test for New Projects. (VAT)
