Omar Mohammad Ahmad Abour
Russeifa
Summary
Over Senior Analyst, bringing a strong foundation in data integrity, time management, and regulatory compliance. Skilled in monitoring updates to pharmacopoeias and standard operating procedures to ensure continued adherence to industry standards. Possess approximately one year of hands-on experience in Computer System Validation (CSV), with a solid understanding of GxP and data lifecycle requirements.
Currently serving as an In-Process Control Supervisor in the CRO (Clinical Research Organization) field, with proven success in supervisory responsibilities, regulatory compliance, and workflow oversight. Adept at leading teams, ensuring operational efficiency, and maintaining high quality standards in a regulated environment.
Overview
9
9
years of professional experience
Work History
In Process Control supervisor
Pharmaceutical Research Unit
Amman
06.2025 - Current
- Supervisory Skills
- Quality Control
- Good Laboratory Practice (GLP)
- Good Clinical Practice (GCP)
- Data Integrity
- Quality management system
- Quality System Compliance
- Deviation Management
- Change Control
- SOP Development
- Quality Auditing
- Logistics Management
- Team Leadership
- Problem Solving
- Calibration
- Troubleshooting
- In Process Control
- Checking on spot
Computer System Validiation Senior Officer
Dar Al Dawa
Amman
09.2024 - 05.2025
- Quality Control
- Data integrity
- Computerized System Validation (CSV)
- U.S. Title 21 CFR Part 11 Regulation
- Good Manufacturing Practice (GMP)
- Equipment Qualification
- Quality System Compliance
- Leadership
- Quality Management.
- Microsoft Office
- SAP ERP
- Good Laboratory Practice (GLP)
- Documentation Practices
- GAMP 5
- Corrective and Preventive Action (CAPA)
- Deviation Management
- Problem Solving
- Change Control
- Troubleshooting
- Qualification Testing
- Laboratory Skills
Senior Analyst
Pharma International
Amman
05.2021 - 09.2024
- Data Reviewer.
- Checking on performance qualification for HPLC, UV spectrophotometer, Dissolution tester and physical instrumental.
- Follow up with analysts on data integrity, GLP, GDP and ALCOA++.
- Issue report investigation out of specification/trend.
- Follow up of production plant and coordination with it on plan of work.
- Modification and development of Standard Operational Procedures.
- Distribution of tasks and jobs on the analysts.
Analyst
Pharma International
Amman
10.2017 - 05.2021
- Analysis of products in all form (Liquid, semi solid, tablet and capsules) and all cases (in process and finished product).
- Apply to GLP, GDP and ALCOA+.
- Read and understand test procedure.
- Knowledge and understanding data integrity.
- Doing performance qualification for HPLC, UV spectrophotometer, Dissolution tester and physical instrumental.
- Working on different instrument such as (HPLC, UV spectrophotometer and IR).
Analyst
Dar AlDawa
Amman
05.2016 - 10.2017
- Analysis of products in form (tablet and capsules) and all cases (in process and finished product).
- Apply to GLP, GDP and ALCOA+.
- Read and understand test procedure.
- Knowledge and understanding data integrity.
- Working on different instrument such as (HPLC and UV spectrophotometer).
Education
Bachelors - Chemistry
University of Jordan
06.2016
Skills
- Capable of multitasking
- Problem Solve
- Microsoft Applications
- Team Work
- Creative
- Working under pressure
- Troubleshooting
- Time Management
- Good Communication Skills
- Leadership Skills
Languages
- English
- Arabic
Timeline
In Process Control supervisor
Pharmaceutical Research Unit
06.2025 - Current
Computer System Validiation Senior Officer
Dar Al Dawa
09.2024 - 05.2025
Senior Analyst
Pharma International
05.2021 - 09.2024
Analyst
Pharma International
10.2017 - 05.2021
Analyst
Dar AlDawa
05.2016 - 10.2017
Bachelors - Chemistry
University of Jordan