1. TASKS
1.1. Management of the execution of the projects by the Specialists, Quality Assurance
1.2. Verification of the work of the Specialists, Quality Assurance
1.3. Management of Standard Operating Procedures (SOPs / SOPs) of clients
1.4. Management of internal procedures
1.5. Management of stability study protocols
1.6. Management of various validation protocols (transport, processes, etc.)
1.7. Maintenance of the internal quality system and that of the customers
1.8. Management of the internal change control and that of the customers
1.9. Management of quality complaints
1.10. Management of investigations and risk/impact evaluation
1.11. Direct interaction with customers
1.12. Release of pharmaceuticals, natural health products and cosmetics on the market
1.13. GMP training to employees and customer staff
1.14. Management of Annual Product Quality Review programs
1.15. Verification and management of different deviation reports
1.16. Self-inspections of clients
1.17. GMP audits of manufacturers and subcontractors
1.18. GMP audits of raw and packaging material suppliers
1.19. Management, verification and execution of all GMP related tasks
1.20. Maintain liaison with the Regulatory Affairs Department
2. MININAL REQUIREMENTS
2.1. BAC in a related science
2.2. Ten to fifteen years of GMP experience involving all dosage forms
2.3. Ten years of experience in personnel management
2.4. Ability to manage multiple projects
2.5. Strong organizational and communication skills
2.6. Strong ability to solve problems
2.7. Available for travel
2.8. Excellent French-English bilingualism, spoken and written
