Bachelor degree in engineering/science or relevant Very good in English reading, writing, and communication. Experienced in Microsoft Office (Word, Excel, Power Point)Strong communication skills with different levels and departments. Professional in creating and reviewing validation protocols, reports, and dashboards Strong knowledge of manufacturing processes (for sterile and non-sterile manufacturing)High level of leadership skills Strong understanding of regulatory requirements related to validation (FDA, EU, WHO)Familiar with Gx P compliance. Familiar with calibration and qualification software Self-learning and team motivator. Professional for multitask follow-up. Manufacturing equipment qualifications (IQ, OQ, PQ)HVAC qualification and area classification (ACR, DP, PAO testing, viable testing, etc.)Qualification and calibration risk assessment Aseptic process simulation Thermal mapping (sterilizers, storage area, and controlled chambers, etc.)Process validation Cleaning validation Monitoring, recording, and logging instruments calibration Preferable to have experience in: Analytical instrument calibration and qualification experience CSV
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