Myriam Azizi

Senior Manager Quality

Myriam Azizi

Senior Manager Quality

Key Knowledge Areas:

  • Certification of promotional information 
  • Quality Management on Exploitant site  
  • Quality approach and continuous improvement management 
  • Educational engineering 

Myriam Azizi Quality Manager PharmaBlue


Myriam earned a PharmD from the University of Paris-Sud (2013) and later a Master’s degree in Quality Management. 


About Myriam 

She is Quality Manager at PharmaBlue within the BlueReg Group managing quality systems. She is responsible of the maintenance of PharmaBlue´s quality system (documentation, initial and continuous training, deviations, CAPA, change controls, quality reviews, internal and external audits). She manages the product complaints process and batch follow-up. 


Myriam also contributes to third parties’ business continuity and to effective functioning of PharmaBlue (enhance efficiencies of quality process).


Myriam has a broad experience in quality management and project management gained through several years of experience working within the pharmaceutical industry. 

Background/Past experience 

Before joining Blue Reg, Myriam worked as a Quality Consultant at Bon Usage Conseil (2012 -2019) in Boulogne-Billancourt, where she supported several Exploitant companies to obtain and maintain the certification for their promotional activities: compliance of their quality system documentation, implementation of management tools, quality management reviews. She also participated to optimize internal process and conducted several audits. 


As Head of Consultancy function of Bon Usage, she was responsible for coordinating consulting services, performing audits and study engagements, managing quality and regulatory project consultants, and identifying development areas for the service function.  


Prior to that, Myriam worked as a Quality Assurance Officer at Stallergenes (2011 – 2012) in Antony, France. She was in charge of qualification and validation of analytical equipment and information systems on a GMP site as well as preparing quality documents (procedures, instructions, forms) for the analytical department..