Mohamed Ashraf Momtaz

**th Ahmed Fahmy St. Ain shams, Cairo

***- 010********

ac3geu@r.postjobfree.com

CAREER OBJECTIVE

Joining an innovative team where my experience, creativity and skills can make a difference. PERSONAL INFORMATION

Date of Birth: Dec 14, 1987

Marital Status: Married

Military Service: Exemption (Only Son)

EDUCATION

Faculty of Science, Tanta University,

Diploma in analytical chemistry also enrolled in Master's Degree.2015 Bachelor of Science Degree (Chemistry Major) 2009

Grade Point Average: Good

EXPERIENCE

Company: Genuine Research Center (GRC) April 2014 – present Adress: 50 El-KhalifaEl-Mamoonst., Heliopolis, Cairo, Egypt Department: Quality Control “Biowaiver”

Job Title: Analyst

Job Description:

Conducted full in-vitro comparison study of our products versus brand product to assess the similarity of our product to that of the patent.

Developing techniques for the analysis of drug products and chemicals; using a range of analytical techniques, instrumentation and software ”analytical method development & validation”

Analyzing samples from various sources to provide information on compounds or quantities of compounds present.

Validating methods and equipment.

Interpreting data and adhering to strict guidelines on documentation when recording data and reporting scientific results.

Designed, developed, validated and implemented stability indicating analysis method. Company: Delta Pharmaceutical Industries (Delta Pharma) February 2013 – April 2014 Adress: 10th of Ramadan City, Al Sharqeya

Department: Quality Control

Job Title: Analyst

Job Description:

- Completes routine testing of in-process, final, validation and stability samples for human and veterinary sector in accordance to SOPs for product release and validation.

- Release finished products from the production hall after analysis ( syrup,semisolid,tablet and sterile )

- Participate in establishing and verification of computerized calculation system by Excel sheet for bulk products

- Audit quality processes and systems and ensure corrective actions are taken.

- Have an idea about: dispensing area, granulation,mixing, compression and coating for tablet (F.C&S.R coating), liquid preparation (syrup &suspension), homogenous of oil& aqueous preparation, packaging (primary

&secondary).

- Troubleshoot routine and non-routine problems encountered in product testing

- Monitoring and ensuring that GLP is followed in the Laboratory

- Ensuring that required reference standards, chemicals, columns, working standards, etc are available

- Aids in the development of test methods.

- Conducts data review and preliminary evaluation of results

- Use different modern methods of analysis and techniques and able to operate the following instruments: High performance liquid chromatography (HPLC) (Agilent, Waters, Shimadzu ),gas chromatography (GC Agilent),near Infra-Red apparatus (NIR),dissolution apparatus, Potentiometer apparatus -disintegration apparatus-hardness apparatus for tablets-refract meter apparatus, friability apparatus-Karl Fischer Apparatus-spectrophotometer apparatus(Normal use).,pH meters, conductivity meter-viscometers, analytical balances and Melting point tester.

Company: Delta Pharmaceutical Industries (Delta Pharma) August 2012 – February 2013 Adress : 10th of Ramadan City, Al Sharqeya

Department: Quality Control

Job Title: Analyst

- Preparation and reviewing of validation protocols and reports.

- Responsible for in process control and monitoring critical parameter for validation batches.

- Operating Procedures (SOPs) and area parameters (Pressure, Temperature,Relative Humidity ...etc)

- Reviewing and assessing the impact of any changes in process or equipment on the corresponding validation status.

- Follow up & maintain the calibration program for all instruments related to the manufacturing process such as:Weights, Sensors and Balances,also validation program for machines like tunnel,autoclave,sip,,,others

- Provide validation support to plants for new projects assigned.

- Participate in validation team (process-cleaning validation :prepare validation protocols and reports

- Perform weight check for the dispensed raw material prior to preparation processes.

- Perform in-process checks at production area (solid department-semisolid soft gelatin )

- Assure product compliance with specifications and proper documentation during production process.

- Assure employees commitment to cGMP .

- Checks for the presence of approved SOPs and check their implementation at the production area and warehouse .

- perform protocol & report of cleaning validation including the master plan and detect the sample plane & critical parameters then implementation the results Company: Egyptian Matches Co. December 2009 – August 2012 Adress: 10th of Ramadan City, Al Sharqeya

Department: Quality Control

Job Title: Chemist

Job Description:

- Analyzing incoming raw materials.

- Supervising different stages of production.

- Conducting various quality tests on the finished product to ensure that it matches both of British and Egyptian standards.

- Developing methods of analysis (Methodology) to detect and determine chemicals.

- Training junior Q. C. Analysts on using instruments such as: viscometer, sieves shaker, pH meter & Conductivity meter.

- Supervising the entire night shift.

TRAINING

- Workshop in Drug manufacturing and registration in faculty of pharmacy Cairo university

- Malaysia compliance program and IT requirements

- Good laboratory practice GLP

- Validation training according to GSK compliance.

- ISO 17025/2005 training.

- Professionally trained on computers’ maintenance incliding ICDL - in E-T Propaganda Co. & World Center for Computers (Supervised by Banha Electronics Co.), Tanta 2008

- Trained in Kafr El Zayat Pesticides & Chemicals Co., in Quality Control Department My summer training was about basic laboratory tests such as: Volumetric titrations, spectrometry & Hardness of water 2011 LANGUAGE & COMPUTER SKILLS

- Obtained level (12 out of 16 levels) according to the American university in Cairo (AUC) .

- Training on soft skills in Emak Academy (training lasted one month)

- Aware of global guidelines ICH,IUPAC,USP,BP)

- Excellent files management skills

- Professional user of Microsoft Office packages (All editions till 2015).

- Good user of different technical program like (Quality Companion, Minitab & ChemSketch, others

- Occasional nights, weekends and holidays may be required.

- Aware of and keeping up to date with, health and safety issues.

- Working collaboratively in cross-functional teams.

Contact this candidate