Raed Ibrahim Abd Al Rahman

Address: JEDDAH SAUDI ARABIA

Mobile no : 009***********

E-mail address: ad0ubs@r.postjobfree.com

ad0ubs@r.postjobfree.com

Experience:

From July 2018 till now Production Manager at ALRAI PHARMA JEDDAH KSA.

-Perform assigned communication responsibilities.

-Planning and organizing production schedules with planning manager.

-Follow up the implementation and end the approved production orders .

-Guidance of GMP practice in production.

-Overseeing production processes and trouble shooting.

-Sharing and reviewing process validation and cleaning validation with other departments.

-Reviewing and check new and updated SOPs,BMR &BPR.

-Follow up track and trace (serialization ) system for finished product and delivering to WH.

-Suggestion of coast saving in manufacturing activities .

-Coordination with R&D department for pilot patches in production.

-Organizing the repair and routine maintenance of production equipment with Engineering manager Department .

-Maintain office files and records, including perpetual inventory for stock.

-Estimating budgets and timescales for production and assessing project and resources requirements.

-Training production staff on production processes and coordinating internal and external training for production staff .

-Coordination with the Human Resources Department on training courses both internally and externally.

-Coordination with the Human Resources Department on periodic medical examinations .

-Follow up g and Coordination with the Human Resources Department for working hours and staff vacations.

June 2016 – April 2018 QA supervisor in SAUDI PERFUME&COSMETIC CO LTD (SPCCL) KSA

-Monitoring Applying GMP in all department .

-Preparing SOPs for different department.

-Reviewing new design and approving it.

-Inspection of receiving PPM & SPM and release .

-NCR, deviation procedure.

-Retain sample collecting .

-Customer complain investigation.

-Daily quality tour .

April 2007 – September 2015: Section Head Solid Dosage Form Department EIPICO - Egypt

-Suggestion for solving problems during compression, capsule filing, Bottles Filing till final solution.

-Suggestion for personal, materials flow in production area to avoid the mix-up, Cross contamination.

-Design of production plant of pharmaceutical products (buildings, instruments, and machines), and

-Design of clean room and containment areas.

-Management Of Validation ( Cleaning – Process )

-Share in Planning of Top Quality; Managing the Quality Function

-Production planning & Coordination local market, export & tenders annual plan

May 2000 - March 2007: Production supervisor solid dosage form,Powder Department EIPICO - Egypt

-Prepare the Documents (SOPs) related to Manufacturing and Packaging.

-Tablet preparation, compression, coating, striping and packaging.

-HG capsule (preparation, filling and packaging).

-SG capsule (filling and packaging).

-Eff. Tab. And powder (preparation, compression, filling and packaging).

-Training the operators about the basic of GMP including personals hygiene, cleaning, and operation.

-Coordinate the handling of raw material,packaging and finished product between production and warehouse

-Check the clearance of the lines before and after processing.

-Prepare the handling of repackaging process from receiving to finial delivery to storage area .

-Check the setting parameters which have effect on the quality of the products like: pH, moisture contain, hardness, friability, disintegration, Wight variation, volume, compression force, leakage,

-Reviewing the batch record before delivery to warehouse..

-Prepare and reviewing the reconciling of batch products.

-Check the all log book for operations and cleaning.

-Member in the team of process and cleaning validation.

April 1997 - April 2000 Quality Assurance Specialist EIPICO - Egypt

1)Processing Activities:

-Reviewing Batch Materials before production operation with production responsible person.

-Withdrawing all samples needed from analysis purposes, send them to QC for Analysis & receiving the analysis certificate from QC & submit it to production responsible person.

-Follow up & check finished product quality in all processing steps

-Ensure that all production rooms are ready for processing through checking appropriate approved forms.

-Check, follow and control production personnel behavior, gowning, hygiene, before production entrance.

-Check recording processes in appropriate form & Sign. If needed, for this.

-Check cleaning procedures of Machine parts & withdraw samples for analysis purpose.

2) Packaging activities:

-Check & follow up all packaging activities.

-Ensure that all records are appropriately filled in time & line clearance checklist is performed.

-Perform physical inspection for semi-finished products on regular basis.

-Perform printed packaging materials check on regular basis & record that in approval forms.

-Check sealing state of blisters, Sachets according approval SOP & record that.

-Check preparation steps of packaging materials such as leaflet folding, overprinting, etc.

-Check and approve the overprinting order for packaging processes.

3) Finished Product in Packaging Area:

-Check the cartooning process, and product identification label for ready finished product for delivery to warehouse.

-Withdraw Stability Samples as specified in approval SOPs and submit them to QC Lab.

4) Initial and final Batch record review

5) Preparing SOPs (Standard Operation Procedures)

20TH OCT 1996 – ABRIL 1997 QC ANALYST IN PHARMACEUTICAL IND.(EIPICO.COPAMNY

HPLC,GC,UV & Titration ANALYST.

Raed Ibrahim Abd El Rahman

Address : JEDDAH KSA

Mobile no : 009***********

E-mail address : ad0ubs@r.postjobfree.com : ad0ubs@r.postjobfree.com

Personal Data:

Nationality : Egyptian

Marital Status : Married

Education:

Faculty : Science

Major : Special Chemistry

Graduation year : 1995

Post Graduate diploma BIO Chemistry and Physiology 2011

Training and Previous Courses:

Basic principles of GMP – CGMP Consideration

Validation System &Cleaning Validation

CAPA & Deviation System

Clean Room Specifications (Contamination – Cleaning Of Aseptic Area )

Air Classification – Water Station

Good Storage Practice ( GSP )

Supplier Evaluation

Hazard Material Management

Integrated Management System

Course with certificate in lead auditing in ISO systems 9001, 14001, 18001

ISO 9001:2015 transaction training SGS ACADEMY

Languages: Arabic & English: Very good

Computer Skills: Windows, Internet, Word, Excel

Driving license: Holds. A driving license

TRANSFERABLE IQAMA: AVILABLE

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