-Graduate or Post Graduate in Lifesciences or B. Tech Engineers, -At least 2-3 year experience in Medical Device/IVD industry. -Exposure to Medical Device Quality Management System, ISO 13485 documentation and Certification Process and GMP. -Previous experience in Diagnostic Manufacturing industry is preferred. The main responsibilities will include: Managing quality oversight (on-site) of all manufacturing activities. Ensuring that quality management system is being maintained and followed. Organising ISO and GMP Audit by various regulatory bodies Language: Fluency in English is must, knowledge in Arabic will be good. Job Types: Full-time, Permanent
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