Support pharmaceutical quality assurance at Apotex in Toronto through GMP oversight, batch review, and cleaning validation activities. Coordinate production quality documentation.

This Coordinator supports quality systems across compounding, sterile filling, non-sterile filling, and packaging. The work includes in-process bulk testing, batch record review, and validation documentation. You will use SAP, LIMS, and Trackwise while supporting investigations and CAPAs.

Key Responsibilities:

- Review sterile and non-sterile production documents
- Provide QA oversight on production lines
- Support investigations and CAPA implementation
- Coordinate cleaning validation sampling activities
- Record batch receipt, review, and release

Requirements:

- Related college diploma or university degree
- Minimum two years pharmaceutical quality or production experience
- Knowledge of GMP and quality requirements
- Robust English verbal and written communication
- Flexibility to work shifts

Apply pharmaceutical quality knowledge, GMP oversight, and documentation skills as a Coordinator supporting Apotex manufacturing operations.

📌 Pharmaceutical Quality Assurance Coordinator (Canada)
🏢 Apotex
📍 Canada