Job Purpose
Participate in the testing plan and follow up in all chemistry laboratory operations & assigned teams, ensuring adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), safety and security measures.

Responsabilities:
1. Monitors records of all deviations/investigations and secures they are properly logged on the system before sending for final validation.
2. Follows up on the closure of deviations/investigations and CAPA implementation within the team. When needed, proceed with team training in coordination with QCL Team leader/Supervisor.
3. Ensures that CAPA related to the Quality Control department are followed properly and executed on time. (Extended or closed on time)
4. Generates monthly report to QC manager on the effectiveness of personnel training and performance based on the number of investigations.
5. Generates monthly report to QC Manager for the number of incoming batches for testing per month and the time allocated to perform the test at both sites Zouk and Zekrit.
6. Monitors chemistry section and Microbiology SOPs status (When needed) and follows up with relevant personnel to secure completion/update.
7. Support the inventory controller in securing the inventory of reagents, standards, Spare parts, glassware’s and supplies. Ensure their good storage as per classification/SOP.
8. Support the Instrumentation team in executing machine’s qualifications and environmental mapping when needed.
9. Assist in preparing, updating and reviewing QSMs as per the yearly plan under the coaching of QC manager.
10. Assist QC manager in any study related to QC department i.e Addition of new equipment/ BC Review, logbook and archive management, Lab extension- Zekrit, Departmental objectives…
11. Review of Analytical laboratory report for Finished product and Raw materials when needed.
12. Performs any task in line with his/her competencies, in the Quality Control department, as required by the management according to department’s/ company’s objectives.
13. Abide to company ethics, compliance and quality requirements and procedures.

Qualifications:

BS in Pharmacy, Chemistry
3 to 5 years of experience
Problem solving
Detailed oriented
Collaborative