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Process Engineer - Chemical Engineer


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Education: 4
Experience: 7 years
Relocation: Yes - Internationally

Industry Experience
3 years Process Engineer
3 years Other
1 years Quality Control/Quality Assurance Engineer

Career Objective

to be a member of yor team


Professional Experience

Professional Experience

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)

 

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