Rami Sawalha

Formulation Scientist at MS PHARMA
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Contact Information
us****@****om
(386) 825-5501
Location
JO

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Experience

    • Jordan
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Formulation Scientist
      • Jan 2022 - Present

    • Manufacturing Supervisor
      • Jul 2019 - Present

    • Manufacturing Supervisor
      • Jul 2019 - Jul 2019

      • Working on lyophilizer system specifically on preparations that need partial closure.• Performs all aspects of lyophilization preparation such as Clean in Place (CIP), Steam in Place (SIP), and leak tests • Troubleshoots or repairs mechanical failures / faults with the lyophilization systems. • Proactively evaluates system functionality to identify and prevent possible system issues that may result in equipment downtime.• Weighing and preparing sterile preparation.• Control products that need acidity titration.• Commitment to the conditions and environment needed by sterile area.• Preparing aseptic and terminal product.• Sterilization autoclave issues by following the principles used to sterilize product.• Follow-up to check autoclave on a daily basis by examining the Bowie-Dick Test and leak test.• Finish and calculate the percentage of the patch record from manufacturing to package

    • Jordan
    • Pharmaceutical Manufacturing
    • 500 - 600 Employee
    • Manufacturing Team Lead
      • Feb 2017 - Jul 2019

      • Performing quantitative and qualitative analysis of raw material, finished products, stability, process validation, and cleaning validation samples, using analytical instrumentation such as UPLC, HPLC, TLC, UV/VIS, PH metry analysis, Karl fischer• Performing GMP review of laboratory products • Revise test methods and SOPs• Having in depth knowledge of chromatographic analysis such as tailing factor, resolution, peak purity, purity angle purity threshold, capacity factor, theoretical plate count

    • Pharmaceutical Manufacturing Team Lead
      • Aug 2011 - Jul 2019

    • Manufacturing Team Lead
      • Aug 2011 - Mar 2017

      • Performed pharmaceutical manufacturing operations in FDA and GMP environment• Operated various manufacturing and processing lines in various Manufacturing -Departments including:o Receiving and delivering the primary and secondary materials within the followed steps from preserving material and checks on the code number And QC number and EXP date and weight of materials and the number of material.o Manual to Semi-automatic manufacturing and packaging, wet and dry weigh & fill-line equipment, agitators, dispensers, liquid and solid encapsulation, compression, rolling, packaging and labeling to produce products including tinctures, lotions, capsules, vape pens and pre-rolls.o Hand-on experience in operating Klockner, Hoonga , Gea800 , Gea300 , Mixing Gea , Bosch Cartoning • Maintain a safe work environment, actively contributing to continuous improvements.• Perform weigh and dispense activities of finished product, active ingredient(s), raw materials and excipients.• Document all manufacturing activities consistent with Good Manufacturing Practices (GMP).• Perform manual manufacturing activities as required.• Observe, monitor & record temperature, pressure and other parameters on Manufacturing processes and equipment.• Perform minor equipment and process maintenance activities.• Communicate daily and effectively with the Manufacturing Manager, Supervisor and Operator peer group.• Maintain personal training status and records consistent with company policies and procedures.• Follow the daily, weekly, and monthly program.

Education

  • Jami'at Al-Zaytoonah Alordunia Al-Khassa
    Bachelor's degree, Pharmacy
    2012 - 2017
  • Alarabiyya College
    Diploma, Pharmacy
    2009 - 2011

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