Lynda Ibrahim

Managed and drafted the annual supplier quality review for packaging materials, adhering to GMP and internal standards.

Comprehensive supplier performance analysis: accepted/rejected batches, NC, deviations, CAPA, OOX, change requests, and audits.

Document verification and consolidation: certifications, approvals, qualifications, CoA, CoC, technical data sheets.

Quality data processing (SAP, GoTrack, IDEA For Con), trend analysis, and proposal of improvement actions.

Drafting and updating quality documentation (procedures, investigation forms, specifications, etc.), with communication of summaries in English to QA/QC teams.

Led awareness training sessions on GMP, GLP, HACCP, and ISO 22000 for all staff: prepared materials, created post-training tests, monitored effectiveness, and regularly updated content.

Complete update of the HACCP plan: hazard analysis, review of flows and uses, definition/adjustment of PRPs, identification of PRPs and CCPs, update of critical limits, monitoring plans, corrective actions, verification/validation, and records, with supervision of on-site implementation.

Deployment of a hygiene charter: design, communication (posters), explanation sessions for operators, on-site monitoring, and reduction of deviations in internal audits.

Supervision of customer/supplier complaints: data collection and root cause analysis (Ishikawa, 5P...etc.), implementation of corrective/preventive actions, effectiveness monitoring, and inter-departmental communication.

Study of the biosynthesis pathways of anti-cancer alkaloids in the plant Catharanthus roseus. Production of recombinant proteins from Escherichia coli. Implementation of several techniques (In vitro culture, French Press, Bradford, Western Blot, Rt-PCR, HPLC, and immunohistochemistry).