Houria El Ibrahimi

-Monitoring of ISO/IEC 17025 implementation -Writing procedures and work instructions -Follow-up of non-conformities and corrective actions -Tracking quality objectives and KPIs -Participation in internal and external audits -Scheduling calibrations and equipment verifications -Managing quality and metrology documentation -Ensuring equipment traceability -Raising staff awareness on quality requirements -Preparing management review reports

-Management of qualification files and method validation according to ISO/IEC 17025. -Follow-up on equipment deviations and calibration schedules. -Measurement uncertainty calculations. -Calibration of pH meters, conductometers, and temperature chains. -Preparation of standard solutions. -Documentation and traceability of technical records in compliance with ISO/IEC 17025.

Analysis and Optimization of Calibration Intervals for Equipment According to Standard FDX 07-014 : -Utilization of Drift, OPPERET, and Periodicity Methods to Optimize -Calibration Intervals -Development of Calibration Procedures for Balances and Glassware.

-Treatment of phosphogypsum -Exploration of phosphogypsum treatment methods - Analysis of treatment effectiveness Recommendations for sustainable management

-Pharmaceutical Waste Management -Regulatory monitoring of the pharmaceutical waste destruction procedure. -Development of an action plan to reduce waste. -Calibration of balances.

Contribution to the implementation of a management system in accordance with ISO/IEC 17025 -Implementation of the PDCA approach. -Establishment of a confidentiality agreement. -Development of a quality policy. -Creation of job descriptions. -Implementation of a procedure for document and record management.

-Performs and processes biological samples for biomedical analyses according to medical prescription, for the purpose of diagnosis, screening, treatment, prevention or research.