Morcos Loka is a Quality Senior Manager for Biologics F&F and New Projects, and previously served as Training Manager & GMP Advisor at Minapharm. Over 25+ years, Morcos has played various production and quality roles in the pharmaceutical and biopharmaceutical industries. His experience includes the manufacture of sterile and non-sterile products, handling regulatory and customer audits, conducting internal and supplier audits, GMP gap analysis, GMP training, GMP consultation, establishing quality management systems, management review, quality metrics, establishing quality risk management systems, and QRM studies, including the manufacturing of HPAPIs in shared facilities and the design of pharmaceutical and biopharmaceutical manufacturing facilities.
Morcos has a Master in Business Administration (MBA), a B.Sc. (Hons) in Pharmaceutical Sciences, two postgraduate diplomas in Total Quality Management (TQM) and Train the Trainer (ToT), and four professional certificates: ASQ Certified Manager of Quality/Organizational Excellence (CMQ/OE), Certified Quality Auditor (CQA), Certified Pharmaceutical GMP Professional (CPGP), and ISPE Certified Pharmaceutical Industry Professional (CPIP).
Morcos is a member of ASQ, ISPE, and PDA. He has participated in various ISPE and PDA publications and has been a speaker at different IVT, ECA, PDA, and ISPE pharmaceutical industry conferences.