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
Solid 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.

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