Kirollos Attallah Metyas

Eva Pharma

• Senior Quality Assurance SpecialistFull Time

  Nov 2023 - Present -1 yr, 7 months

  Egypt , Sharqia

  • Job Details:Duties: • Prepare validation master plans. • Develop and execute process validation protocols and reports. • Review IQ, OQ, and PQ documents for equipment qualification. • Perform and oversee the required qualifications / requalification for Air Handling Units (AHUs), Production Machines, Laboratory Equipments, & Water Treatment Plant (WTP) • Review cleaning validation reports. • Perform HVAC validation activities. • Execute temperature mapping and prepare final reports. • Follow up on the calibration of all equipment as per the annual CMP • Handle calibration activities for all departments with third-party organization • Perform compressed air validation and calibration activities. • Manage site documentation system and conduct training. • Review and release production batches on Oracle. • Review issued deviations, review investigations, and related CAPAs. • Organize and participate in internal audits and CAPA reporting. • Train newly hired Quality Assurance Specialists. • Review Quality Control COAs on LIMS system. • Review batch records and laboratory reports for release. • Evaluate change control requests, ensure proper documentation, and assist in execution
• Senior Quality Control SpecialistFull Time

  Jun 2023 - Nov 2023 -5 months

  Egypt , Sharqia

  • Job Details:Duties: • Prepare quality control lab reports for raw, packaging materials, and finished products. • Maintain and troubleshoot QC instruments. • Review analytical method validation reports. • Monitor stability activities and review related reports. • Train newly hired Quality Control Specialists. • Review working and reference standard certificates. • Monitor quality control laboratory chemicals consumption and stock.
• Quality Control SpecialistFull Time

  Jun 2021 - Jun 2023 -2 yrs

  Egypt , Cairo

  • Job Details:Duties: • Perform analysis of raw, packaging, and finished products. • Participate in the process of validation of new and revalidated products. • Perform analytical method validation and technical transfer activities. • Conduct performance checks for laboratory instruments (HPLC, UV, TOC, etc.). • Review annual performance qualification reports of instruments. • Prepare mobile phase and buffer solutions.