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DAWOOD FAISAL AL-JAMAL
PERSONAL DETAILS
Date of Birth 19-05-1986
Nationality JORDANIAN
Driving Licence Sharjah Driving licence number (400170)
Contact Number 00971567467146
Email Dawood.aljamal@gmail.com
LinkedIn https://ae.linkedin.com/pub/dawood-al-jamal/40/2a9/a26
EDUCATION AND TRAINING
Date: June 2009 University - Bachelor of Science in BIOTECHNOLOGY & GENETIC ENGINEERING
From JORDAN UNIVERSITY OF SCIENCE & TECHNOLOGY, Jordan.
Date: August 2009 Course: Training course in Real-Time PCR “Principle & Application”
At The Centre of Consultation in the Jordan University
Date: 15-03-2009 till 15-04-2009 Course: Trained in Laboratories Division / Medical Dept.
At King Abdullah University Hospital
Date: 23-07-2008 till 07-08-2008 Course Hands on Assisted Reproduction Technology (IVF/ICSI)
Course from IVF & GENETICS CENTER at JORDAN HOSPITAL
Date: 22-06-2008 till 22-07-2008 Course Trained in the IVF unit at THE FARAH HOSPITAL
CAREER HISTORY
GULF PHARMACEUTICAL INDUSTRIES (JULPHAR), Ras Al Khaimah, UAE
from June 2010 – (Still on the head of my work)
Research Officer
 Lead the analytical team in the biotechnology development lab
 Check and evaluate the data of analytical reports of in-process and final bulk samples according to the
procedures.(Processing and Analyzing Erythropoietin and Insulin samples through different analytical test)
 Prepare /review/check of in-process and final bulk products SOPs and Specification Methods and ensure
their conformance to the compendial and regulatory requirements.
 To execute lab qualification, analytical method development and method validation activities.
 Prepare SOPs (Standard Operating Procedure), and STMs (Standard test methods) to make sure that
these documents are used whenever and wherever applicable.
 Maintain and provide work status as well as activity reports to Chief Scientist biotechnology for evaluation in
timely manner.
 Maintain inventory of in-house and compendial reference standards for use in the laboratory.
 Maintain GLP practises in the development lab.
 Development, Standardization, Validation and Verification as per the regulatory for In-process and Final
Purified Product testing.
 Operate many Biotech. & Analytical instrument (Real-Time PCR, HPLC , AKTA System ,VERTICAL &
Automated IEF , Endotoxin clotting test )
SKILLS AND LANGUAGES
 Mother tongue : Arabic Other language : English ( Toefl & IELTS)
 Computer skills and competences : MS Office, Internet searching skill
 Highly motivated, good social communication skills , good team- worker
 Can Handle work pressure & can handle multiple Tasks
REFERENCES
AVAILABLE UPON REQUEST

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DAWOOD C.V

  • 1. DAWOOD FAISAL AL-JAMAL PERSONAL DETAILS Date of Birth 19-05-1986 Nationality JORDANIAN Driving Licence Sharjah Driving licence number (400170) Contact Number 00971567467146 Email Dawood.aljamal@gmail.com LinkedIn https://ae.linkedin.com/pub/dawood-al-jamal/40/2a9/a26 EDUCATION AND TRAINING Date: June 2009 University - Bachelor of Science in BIOTECHNOLOGY & GENETIC ENGINEERING From JORDAN UNIVERSITY OF SCIENCE & TECHNOLOGY, Jordan. Date: August 2009 Course: Training course in Real-Time PCR “Principle & Application” At The Centre of Consultation in the Jordan University Date: 15-03-2009 till 15-04-2009 Course: Trained in Laboratories Division / Medical Dept. At King Abdullah University Hospital Date: 23-07-2008 till 07-08-2008 Course Hands on Assisted Reproduction Technology (IVF/ICSI) Course from IVF & GENETICS CENTER at JORDAN HOSPITAL Date: 22-06-2008 till 22-07-2008 Course Trained in the IVF unit at THE FARAH HOSPITAL CAREER HISTORY GULF PHARMACEUTICAL INDUSTRIES (JULPHAR), Ras Al Khaimah, UAE from June 2010 – (Still on the head of my work) Research Officer  Lead the analytical team in the biotechnology development lab  Check and evaluate the data of analytical reports of in-process and final bulk samples according to the procedures.(Processing and Analyzing Erythropoietin and Insulin samples through different analytical test)  Prepare /review/check of in-process and final bulk products SOPs and Specification Methods and ensure their conformance to the compendial and regulatory requirements.  To execute lab qualification, analytical method development and method validation activities.  Prepare SOPs (Standard Operating Procedure), and STMs (Standard test methods) to make sure that these documents are used whenever and wherever applicable.  Maintain and provide work status as well as activity reports to Chief Scientist biotechnology for evaluation in timely manner.  Maintain inventory of in-house and compendial reference standards for use in the laboratory.  Maintain GLP practises in the development lab.  Development, Standardization, Validation and Verification as per the regulatory for In-process and Final Purified Product testing.  Operate many Biotech. & Analytical instrument (Real-Time PCR, HPLC , AKTA System ,VERTICAL & Automated IEF , Endotoxin clotting test )
  • 2. SKILLS AND LANGUAGES  Mother tongue : Arabic Other language : English ( Toefl & IELTS)  Computer skills and competences : MS Office, Internet searching skill  Highly motivated, good social communication skills , good team- worker  Can Handle work pressure & can handle multiple Tasks REFERENCES AVAILABLE UPON REQUEST