NEW: QA/PV Self Inspection
Exclusive to The Source - register/apply now
Our Canada-based client is seeking an external self-inspection covering its Pharmaceutical Quality Management System/GMP and Pharmacovigilance activities.
Our client operates as an importer and distributor of pharmaceutical and natural health products, with warehouse storage and distribution activities in Mississauga, Ontario, Canada, and no manufacturing capability.
The proposed scope includes assessment against applicable Canadian regulatory requirements.
The Role
G&L requires support for the following PV activities:
- Pharmacovigilance System Master File
- ICSR management and reporting
- Safety database data integrity and validation
- Literature monitoring and signal management
- PSUR, RMP and product quality complaint handling
- Quality management system and CAPA
- Business continuity
- Data Protection
- Key personnel education and training e.g. QPPV/Deputy
Requirements
How to Apply
This contract opportunity is exclusive to The Source.
To apply or request further information, please register or sign in by clicking the button below.
Timeline: The client is targeting completion by late November/early December 2026, ahead of anticipated Health Canada regulatory inspections in 2027.
Location: On-site versus remote delivery is yet to be confirmed.
