Tariq Jawabreh
Crestwood
Summary
Quality Control Supervisor with over 8 years of experience in quality control within pharmaceutical and food manufacturing environments. Experienced in supervising QC activities, ensuring GMP/cGMP compliance, supporting routine laboratory operations, and participating in investigations and CAPA activities. Familiar with stability testing, SOPs, audit support, and continuous improvement to maintain product quality and regulatory compliance.
Overview
8
8
years of professional experience
Work History
Senior QA technician
NLX BEVERAGE SOLUTIONS
New Lenox
10.2025 - Current
- Perform routine line audits and inspections of manufacturing, filling, and packaging processes to ensure compliance with Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).
- Monitor critical control points (CCPs) as defined in the HACCP plan.
- Conduct visual inspections of raw materials, in-process products, and finished goods for defects, contamination, or deviations.
- Collect random samples of raw materials (flavors, sweeteners, water), work-in-progress (WIP), and finished products according to the established sampling plan.
- Perform basic physical and chemical tests in the QA lab, such as: pH and Brix/Acidity measurements, Carbonation levels (for relevant products), Turbidity/Clarity checks, Weight/Volume checks for fill levels, Packaging integrity tests (leak tests, torque tests for caps).
- Prepare samples for external microbiological or nutritional analysis as required.
- Accurately record all test results, inspection findings, and non-conformances in QA logs, checklists, and the company's quality management system (e.g., digital QA software or physical batch records).
- Assist in maintaining and organizing all quality-related documents, including certificates of analysis (COAs) from suppliers, SOPs, and calibration records.
- Support the creation of daily/weekly quality performance reports.
- Immediately report any quality deviations, out-of-specification (OOS) results, or potential hazards to the QA Supervisor/Manager.
- Assist in quarantining non-conforming products and materials.
- Participate in root cause analysis investigations and support the implementation of Corrective and Preventive Actions (CAPA).
- Support audits of cleaning and sanitation procedures for production equipment and the production environment.
- Verify the effectiveness of cleaning by conducting basic ATP swab tests or visual inspections.
- Monitor staff compliance with personal hygiene and GMP policies (e.g., dress code, hand washing).
- Ensure all laboratory and testing equipment (scales, pH meters, refractometers) are calibrated and maintained according to schedule.
- Maintain cleanliness and order in the QA laboratory.
- Manage inventory of QA lab supplies and consumables.
Lead Senior Quality Control (Stability)
Hayat Pharmaceutical Industries
06.2024 - 12.2024
- Lead the team in the operation of HPLC (Thermo Dionex, Shimadzu, Agilent), UPLC, UV spectroscopy, IR, and near-IR spectroscopy, ensuring accurate stability testing of products.
- Guide the use of Atomizer devices and manage the analysis of sterile products for stability compliance.
- Led investigations into deviations, out-of-specifications (OOS), and non-conformances, performing thorough root cause analysis to identify underlying issues and prevent recurrence.
- Oversee the recording of stability testing results in Certificates of Analysis (CoA).
- Ensure the team prepares all related documents, records, and certificates in compliance with regulatory standards, maintaining accuracy and reliability in stability reports.
- Implement and manage Standard Operating Procedures (SOPs) specific to stability testing, ensuring adherence to regulatory guidelines (GLPs, USP, ISO).
- Lead the writing, updating, and monitoring of SOPs for stability testing methods and instruments used by the QC lab team.
- Review all stability-related data and reports from the team, ensuring compliance with specifications and correct calculations.
- Lead troubleshooting efforts to resolve any issues during stability analysis, ensuring the integrity of stability testing results and trends.
- Implement standard operating procedures (SOPs) to ensure compliance with applicable regulations, including GLPs, USP, ISO, etc.
- Supervise the management of stability samples, including entry, withdrawal, and testing in stability chambers.
- Ensure the team follows the monthly stability plan, performs daily checks on temperature and humidity levels in stability chambers, and creates SDS (Stability Data Sheets) for stability results.
- Regularly reviewed the effectiveness of implemented CAPA actions through trend analysis and follow-up audits, ensuring sustained improvements and preventing recurrence of identified issues.
Senior Quality Control
Savvy pharma
03.2024 - 06.2024
- Operate HPLC (Thermo Dionex, Shimadzu), UPLC, UV spectroscopy, IR, and near-IR spectroscopy.
- Use Atomizer devices and perform analysis of sterile products, ensuring compliance with specifications.
- Record results in Certificates of Analysis (CoA) and prepare various documents and records.
- Implement and update Standard Operating Procedures (SOPs) to ensure compliance with regulations such as GLPs, USP, and ISO.
- Review documents, reports, and data from analysts, ensuring accuracy and compliance with specifications.
- Troubleshoot and resolve any issues encountered during analysis.
- Perform daily checks on stability chambers for temperature and humidity, and create SDS for stability results.
- Sample, test, and release finished products according to strict timelines, ensuring compliance with business requirements.
- Monitor and analyze stability samples, checking results against trend data.
Senior Research Analyst (Stability)
Julphar pharmaceutical industry
08.2022 - 02.2024
- Operate HPLC (Thermo Dionex, Shimadzu, Agilent), UPLC, UV spectroscopy, IR, and near-IR spectroscopy.
- Work with Atomizer devices and perform analysis on sterile products to ensure compliance with specifications.
- Record results in Certificates of Analysis (CoA) and prepare various documents, records, and Certificates of Analysis.
- Ensure all reports comply with internal and regulatory standards.
- Review documents, reports, and data from analysts, ensuring accuracy and proper calculations.
- Troubleshoot and resolve any issues encountered during analysis, ensuring consistent quality.
- Create SDS (Stability Data Sheets) for stability results.
- Monitor and analyze stability samples, compare results with trend data, and conduct daily checks on temperature and humidity in stability chambers.
Senior Quality Control
MS pharma injectable
03.2019 - 07.2022
- Operate HPLC (Thermo Dionex, Shimadzu), UPLC, UV spectroscopy, IR, and near-IR spectroscopy.
- Use Atomizer devices and perform analysis of sterile products, ensuring compliance with specifications.
- Record results in Certificates of Analysis (CoA) and prepare various documents and records.
- Implement and update Standard Operating Procedures (SOPs) to ensure compliance with regulations such as GLPs, USP, and ISO.
- Review documents, reports, and data from analysts, ensuring accuracy and compliance with specifications.
- Troubleshoot and resolve any issues encountered during analysis.
- Sample, test, and release finished products according to strict timelines, ensuring compliance with business requirements.
- Monitor and analyze stability samples, checking results against trend data.
- Oversee the receipt and entry of raw and packaging materials in the QC raw materials area.
- Perform analysis of raw materials following industry protocols, and communicate with suppliers to resolve any issues related to analysis procedures.
Quality Control Analyst
Hayat Pharmaceutical Industries
10.2017 - 03.2019
- Conduct in-process checks during production to ensure the intermediate or Active Pharmaceutical Ingredient (API) meets specifications, adjusting processes as needed.
- Perform analysis on physical and chemical properties of various drug dosage forms, including tablets, capsules, syrups, suspensions, creams, and ointments.
- Utilize advanced instruments such as HPLC (Thermo Dionex, Jaco, Thermo TSP), UV spectrophotometer, potentiometer, disintegration apparatus, hardness apparatus, friability apparatus, Karl Fischer apparatus, pH meter, viscometer, melting point apparatus, and refractometer.
- Record results, perform calculations, and document findings in a chemical notebook, ensuring accuracy and compliance with industry standards.
- Prepare and standardize chemical reagents, and conduct analysis of both bulk and finished products, including stability studies.
Education
Bachelor Degree - Chemistry
The Hashemite University
Jordan 10.2012 - 01/2017
Skills
- CAPA
- GMP / cGMP Compliance
- Data Review
- SOP
- OOS/OOT investigation
- FDA regulations
- Documentation control & data integrity
- Process Control
- Troubleshooting
- Audit preparation (internal and external)
Timeline
Senior QA technician
NLX BEVERAGE SOLUTIONS
10.2025 - Current
Lead Senior Quality Control (Stability)
Hayat Pharmaceutical Industries
06.2024 - 12.2024
Senior Quality Control
Savvy pharma
03.2024 - 06.2024
Senior Research Analyst (Stability)
Julphar pharmaceutical industry
08.2022 - 02.2024
Senior Quality Control
MS pharma injectable
03.2019 - 07.2022
Quality Control Analyst
Hayat Pharmaceutical Industries
10.2017 - 03.2019
Bachelor Degree - Chemistry
The Hashemite University
10.2012 - 01/2017