Apply regulatory expertise to pharmaceutical quality assurance in Canada, supporting GMP compliance, product release, and quality systems as a consultant.

This senior consulting position supports pharmaceutical, medical device, natural health product, and clinical trial supply operations. You will coordinate regulatory documentation, collaborate with clients and international manufacturing sites, and contribute to compliant Canadian-market operations. The work includes quality investigations, reporting, audits, and continuous improvement.

Key Responsibilities:

- Maintain DEL, MDEL, SL, and other establishment licences
- Coordinate international site approvals across multiple clients
- Review GMP documentation and product release records
- Manage deviations, complaints, change controls,



and trend analysis
- Support audits, inspections, recalls, and quality reporting

Requirements:

- Bachelor's degree in pharmaceutical or healthcare-related discipline
- At least five years of qualified Quality Assurance experience
- Knowledge of Food and Drugs Act and Health Canada GMP
- Understanding of GCP, GMP, GDP, and data integrity
- Experience with root cause analysis and CAPA

Bring regulatory knowledge, investigation expertise, and quality systems experience to Canadian healthcare and pharmaceutical consulting operations.

📌 Senior Pharmaceutical Quality Assurance Consultant (Canada)
🏢 Jobgether
📍 Canada