Experience

SITEC Information Technology

• Jordan
• IT Services and IT Consulting
• 1 - 100 Employee

• Quality Assurance Manager

  • Aug 2022 - Present

  SITEC Jordan Co. has an exclusive agency to AmpleLogic software, which is interested in DMS and QMS. I'm working on marketing this software to companies to help her with electronic transformation. SITEC Jordan Co. has an exclusive agency to AmpleLogic software, which is interested in DMS and QMS. I'm working on marketing this software to companies to help her with electronic transformation.



Wadi Alrafidain Pharma

• Quality Assurance Manager & ISO Consaltant

  • Oct 2020 - Aug 2022

  Managing the QA department, and giving the necessary training in GMP & QMS rules to the company staff, in addition to following up on the requirements of Iraqi MOH regarding the GMP requirements. Work as a consultant for the QMS requirements in Al-Rafidain Group.

• QA Manager

  • Oct 2020 - Aug 2022



Self-employed

• Amman, Jordan

• QA Manager & QMS Consultant

  • Mar 2017 - Oct 2020

  According my long experience in the quality assurance in the pharmaceutical industries, I providing advice, Follow-up of the quality assurance system and verify its efficiency, by conducting frequent internal audits, and follow-up the application of all requirements to ensure the quality of the final product and the satisfaction of customers, and providing the recommendations to improve work performance and get rid of these problems in a professional manner. According my long experience in the quality assurance in the pharmaceutical industries, I providing advice, Follow-up of the quality assurance system and verify its efficiency, by conducting frequent internal audits, and follow-up the application of all requirements to ensure the quality of the final product and the satisfaction of customers, and providing the recommendations to improve work performance and get rid of these problems in a professional manner.



Pharma International Company

• Jordan
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Head of Documentation in QA Dept.

  • Nov 2001 - Feb 2017

  Manage and supervise all activities in the documentation section / QA dept. Prepare and review documentation system based on GMP and ISO requirements. Control all documents related to GMP and ISO requirements. Ensure keeping the documents and records of GMP requirements to protect access to documents and records under security and privacy rules. Follow up with the latest GMP trends and update the documentation system based on GMP requirements. Ensure compliance of the good documentation practices by the internal inspection of the different technical departments based on GMP and ISO requirements. Prepare the documentation section budget. Evaluate the performance of documentation staff to achieve department goals. Determine training needs for documentation staff. Interview new staff and choose the best candidates for the job requirements. Determine the key performance indicators (KPI’s). Contribute to SWOT Analysis. Receive customer complaints and deal with them according to the applicable system. Show less



TQ Pharma

• Jordan
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Documentation / QA Supervisor

  • Oct 2009 - May 2010

  Make sure that the department documents are identical to the coding and documentation system. Documents data entry in the database system. Distribution and follow-up the documentation technician's tasks. Control of ISO records and logbooks. Preparing ISO documents. and Commitment to applying good manufacturing practices GMP. Make sure that the department documents are identical to the coding and documentation system. Documents data entry in the database system. Distribution and follow-up the documentation technician's tasks. Control of ISO records and logbooks. Preparing ISO documents. and Commitment to applying good manufacturing practices GMP.



Arab Medical Containers/ Hikma Pharmaceuticals Group

• Jordan
• Packaging and Containers Manufacturing
• 1 - 100 Employee

• QA/QC Supervisor

  • Aug 1992 - Nov 2002

  Performing the QC responsibilities such as make testing for all batches (start-up and in-process). Performing the final acceptance release for batches. Taking the samples (start-up and in-process) for testing in QC. Performing calibration for measurement tools (pipe gauge, balances, and caliber ...etc.). Inspection of raw materials and packaging materials received from suppliers. Control of ISO records and logbooks. Preparing ISO documents. and Commitment to applying good manufacturing practices GMP. Show less