1. Management of the execution of the projects by the Specialists, Quality Assurance
  2. Verification of the work of the Specialists, Quality Assurance
  3. Management of Standard Operating Procedures (SOPs / SOPs) of clients
  4. Management of internal procedures
  5. Management of stability study protocols
  6. Management of various validation protocols (transport, processes, etc.)
  7. Maintenance of the internal quality system and that of the customers
  8. Management of the internal change control and that of the customers
  9. Management of quality complaints
  10. Management of investigations and risk/impact evaluation
  11. Direct interaction with customers
  12. Release of pharmaceuticals, natural health products and cosmetics on the market
  13. GMP training to employees and customer staff
  14. Management of Annual Product Quality Review programs
  15. Verification and management of different deviation reports
  16. Self-inspections of clients
  17. GMP audits of manufacturers and subcontractors
  18. GMP audits of raw and packaging material suppliers
  19. Management, verification and execution of all GMP related tasks
  20. Maintain liaison with the Regulatory Affairs Department


  • BAC in a related science
  • Ten to fifteen years of GMP experience involving all dosage forms
  • Ten years of experience in personnel management
  • Ability to manage multiple projects
  • Strong organizational and communication skills
  • Strong ability to solve problems
  • Available for travel
  • Excellent French-English bilingualism, spoken and written