Manage deviations, CAPAs, and root cause analysis for Grifols’ regulated Quality System. Support compliance across Canadian and EMA requirements.

As a Deviation and CAPA Specialist reporting to the QMS Manager, you will oversee quality event management and documentation. The work includes regulatory monitoring, KPI reporting, investigation support, and continuous improvement. You will help maintain compliance with Grifols standards and applicable regulations.

Key Responsibilities:

- Manage approved deviation and CAPA systems
- Coordinate investigations, root cause analysis, and corrective actions
- Track records, timelines, documentation, and quality event closure
- Monitor Canadian, EMA, and Grifols regulatory changes
- Support audits with quality records, metrics, and compliance evidence

Requirements:

- Bachelor’s degree in health-related sciences, preferably Pharmacy
- Minimum two years’ related GMP Quality Systems experience
- Knowledge of Quality Management and preferred cGMP requirements
- Proficiency with computers and Microsoft Office
- Ability to follow, explain, and enforce SOPs

Apply quality systems expertise, regulatory awareness, and CAPA management skills to strengthen compliance at Grifols.

📌 Deviation and CAPA Quality Specialist (Mississauga)
🏢 Grifols
📍 Mississauga