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Malik Abulhija
Amman E-mile alhija2014@gmail.com
Call +972799768178
Personal information
 Nationality: Jordanian
 Place of Birth: Irbid, Jordan
 Date of Birth: 28 of April, 1983
 Sex: Male
 Status: Married with 1 child (age 5)
Educations:
 B.Sc. in Chemistry from the science faculty from the Yarmouk University (2002-2006) Grade: Good.
Certificates of completion:
 Cleaning validation work shop 1-2 Dec 2014 Amman-Jordan by business enabler consulting.
 Computerized systemsoftware validation work shop 07-08- Sep 2015 Amman-Jordan by business enabler.
 Microsoft office excel 2010 (30 hours)19.08.2014 Amman-Jordan by new horizons.
 Advance Chromeleon 7.1 software UHPLC 2-5 April 2014 Germering-Germany by Thermo fisher scientific.
 Enabling powerful leaders and situational coaching and negotiations skills , 6 days Amman –Jordan by
Business Eye Consulting.
 Empowered leadership program 24-25 June 2013 Amman-Jordan by Business Eye Consulting
 Time and stress management 15-16 Sep 2013 Amman-Jordan by Business Eye Consulting.
 Lean workshop in reduce waste and boost yourprofit with the effective 5S program in quality control labs
January-April 2009 Amman-Jordan by Hikma.
 Essential of applied statistics 24 January-13 February 2011 (30 hours) Amman-Jordan by German Jordanian
University.
 HPLC method development based on molecular structure of pharmaceuticals 16-17 August 2009 Amman-
Jordan by Sana pharmaceutical research.
Professional Summary
Total Quality experiences more than nine years.
 Quality control senior analyst for four years, with excellent experiences and knowledge in the analysis of different
types of pharmaceutical drugs utilizing the wet chemistry and different instruments like HPLC, UHPLC, spectrometer.
 Quality control supervisorfor three years, supervise production laboratory.
 Quality control senior supervisorfor two years, supervise production and raw material laboratory till now.

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Experience
 Employed chromatography, spectroscopy and spectrophotometry techniques.
 Improved formulas and processes to increase efficiency.
 Created new laboratory processes.
 Coordinated all personnel involved in testing labs.
 led a team of production quality control, including 12 chemists, 2 lab technicians.
 Led, write and review quality control investigations and reports.
 Conducted both qualitative and quantitative analysis.
 Executed experimental design techniques and evaluation reports.
 Trained junior chemists on different instruments and quality control SOP's
 Evaluated and inspected incoming raw materials.
 Evaluated and follow up process validation for new products.
 Maintained up-to-date records of product technical data sheet and certificate of analysis.
 Create and update methods of analysis and specification sheets.
 Managing the work changing priorities, and others.
 Excellent skills for HPLC analyses and troubleshooting
 Excellent experience in Method Development and method validation - Very good skills for HPLC analysis.
 Capabilities in managing and organizing of work.
 Ability in building of teams and taking the decisions.
 Continued: Create, review quality control SOP's.
 Review and approve the IQ-OQ protocols and change controls of different type of instruments.
 Review and approve the cleaning validation methods and reports.
 Review the standardization reports of working standards.
 Review the instruments maintenance and calibration reports.
 Evaluate and order of different types of QC instruments and consumables.
 Follow the implementation of the new USP/EP/BP monographs and updates.
 Training QC employees on GMP's, GLP's and general regulations.
Skills
 Highly communication skills.
 Computer skills.
 Problem-solving.
 Great organizational skills.
 Excellent knowledge using SAP system.