Apply pharmaceutical quality assurance expertise to regulated client projects, remotely or onsite, across medicinal products, drugs, devices, and natural health products.
The Quality Consultant provides establishment, validation, operational, and other quality assurance consulting services. This work supports regulated industries and draws on scientific knowledge, GMPs, quality systems, and validation experience. Projects span the drug manufacturing and supply lifecycle.
Key Responsibilities:
- Apply scientific and regulated product knowledge to client projects
- Manage pharmaceutical quality system lifecycles and documentation
- Qualify and validate facilities, equipment, and computerized systems
- Conduct supplier quality and GMP evidence audits
- Author compliance approaches for licensing or remediation
Requirements:
- Post-secondary quality assurance or regulatory education
- Knowledge of International and Health Canada GMP terminology
- Experience applying GMP, GLP, GDP, and applicable GCP standards
- Experience developing quality manuals and validation master plans
- Robust organizational, communication, and problem-solving skills
Use quality systems, validation, GMP auditing, and regulated product knowledge across pharmaceutical consulting projects.
📌 Pharmaceutical Quality Assurance Consultant (Canada)
🏢 RQC
📍 Canada