Dr. Azis Shraibi, Eng, has over 25 years of experience in process engineering, layouts, clean systems and utilities, cleanrooms and Validation in various sectors: pharmaceutical, biotechnology, morphine/cannabis, medical devices, natural health products, cosmetics, nutraceuticals, food, pulp & paper, biorefinery & bioethanol. He is an expert referent for Health Canada & MAPAQ, for the implementation of quality systems, but also for facility compliance audits, in accordance with regulatory requirements: GMP/CGMP, HACCP, ISO-22000, SQF, GFSI.
Dr. Shraibi is also a certified trainer by CPMT #0059104. He has been a guest speaker at several pharmaceutical conferences: JFDA, GMP Summit/Omics, A3P, Maghreb Pharma et CIPE.
Dr. Azis Shraibi, Eng, has more than 120 projects in Canada, France, Switzerland, USA, North Africa, involving APS/BOD, detailed engineering: APD, FAT, SAT, commissioning, and qualification. He was Engineering Director at Validapro, SNC Lavalin Pharma, CRIP, Groupe ONA, Cosumar, Baltimar.