Khalándrion, Attiki, Greece
•Employing techniques such as HPLC/Dissolution/Karl Fischer/UV/VIS Spectroscopy. •Performing routine analysis of pharmaceutical products and raw materials. •Implementing method validation and method transfer protocols. •Organization and planning for multiple ongoing projects. •Operating advanced analytical lab instrumentation. •Maintaining and managing accurate and precise documentation according to GMP requirements. •Participating in internal and external audits to ensure compliance with regulatory standards. •LIMS Database Management
•Sterility testing and bacterial endotoxin test (Kinetic method) in semifinal products • Bioburden analysis of water, raw materials and bulk samples •Sampling of water, semi-final and final products •Performance of growth promotion tests on culture media • Data entry, EM reports, data monitoring and trending •Training in Good laboratory practice and Good manufacturing practice •Handling of microbiological wastes •Change Controls •Visual Inspection